Next Article in Journal
Validation and Improvement of a Bicycle Crank Arm Based in Numerical Simulation and Uncertainty Quantification
Previous Article in Journal
Presentation Attack Face Image Generation Based on a Deep Generative Adversarial Network
Previous Article in Special Issue
A Novel Genetically Encoded Single Use Sensory Cellular Test System Measures Bicarbonate Concentration Changes in Living Cells
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Sensing Senses: Optical Biosensors to Study Gustation

1
Institute of Molecular and Cell Biology, Hochschule Mannheim, 68163 Mannheim, Germany
2
BRAIN AG, 64673 Zwingenberg, Germany
3
Interdisciplinary Center for Neurosciences, Heidelberg University, 69120 Heidelberg, Germany
*
Authors to whom correspondence should be addressed.
Sensors 2020, 20(7), 1811; https://doi.org/10.3390/s20071811
Submission received: 29 February 2020 / Revised: 19 March 2020 / Accepted: 21 March 2020 / Published: 25 March 2020
(This article belongs to the Special Issue Disposable Optical Biosensors)

Abstract

:
The five basic taste modalities, sweet, bitter, umami, salty and sour induce changes of Ca2+ levels, pH and/or membrane potential in taste cells of the tongue and/or in neurons that convey and decode gustatory signals to the brain. Optical biosensors, which can be either synthetic dyes or genetically encoded proteins whose fluorescence spectra depend on levels of Ca2+, pH or membrane potential, have been used in primary cells/tissues or in recombinant systems to study taste-related intra- and intercellular signaling mechanisms or to discover new ligands. Taste-evoked responses were measured by microscopy achieving high spatial and temporal resolution, while plate readers were employed for higher throughput screening. Here, these approaches making use of fluorescent optical biosensors to investigate specific taste-related questions or to screen new agonists/antagonists for the different taste modalities were reviewed systematically. Furthermore, in the context of recent developments in genetically encoded sensors, 3D cultures and imaging technologies, we propose new feasible approaches for studying taste physiology and for compound screening.

1. Introduction

On the journey towards understanding the sense of taste, two major parameters have been measured at the cellular level: voltage and Ca2+ changes. Indeed, both types of signals are emitted by taste cells in the periphery and by neurons in the central nervous system in response to a given tastant. All the way up from the tongue to the brain, our body uses an alphabet of voltage and Ca2+ fluctuations to decipher qualities and concentrations of tastants and to instruct decisions on food palatability. These notions have been used to construct and use different types of biosensors for fundamental and applied research.
Biosensors are analytical devices that allow the detection of chemical analytes through the combination of a biological recognition element with a physicochemical transducer [1,2]. Amongst these, cell-based biosensors incorporate sensors (and sometimes also transducers) in living cells and convert the resulting information into digital signals, which are then analyzed by means of specific techniques [2,3]. With respect to taste analysis, cell-based biosensors are also called “bioelectronic tongues” (B-ETs). These are able to analyze tastants in a fast, sensitive and selective way and have been recently designed based on the discoveries in taste physiology [2,4,5]. Since B-ETs are based on cells or tissues expressing taste receptors, they provide specificity, selectivity and sensitivity analogous to the biological sense of taste [5]. So far, transducers coupled to B-ETs use often voltametric/amperometric, potentiometric or piezoelectric methods and thus include microelectrode arrays, field effect transistors or light-addressable potentiometric sensors [5,6,7,8]. Even if these prototype devices have not yet been commercialized, B-ETs have a wide range of potential applications in the fields of drug and food industries, toxicology and biomedicine [3,9,10]. Furthermore, they might become valuable tools for research on taste transduction mechanisms. Finally, their development is tightly linked to the progress in understanding taste physiology.
A second kind of approach that has been primarily applied to basic research on taste sensation uses “molecular optical biosensors” to measure cellular responses to flavor stimulation. In this context, we refer to molecular optical biosensors as molecules that produce light changes in relation to cellular activity, therefore they are suitable to measure functional cell responses. They can be either, chemical fluorophores or genetically encoded fluorescent proteins, that shift their excitation/emission spectra or fluorescence intensity based on specific biological signals, such as changes in ion concentration, voltage, metabolites and second messenger molecules. Molecular optical biosensors are highly sensitive, real-time and simple-to-operate tools, that can be easily monitored with a plate reader for enhanced throughput or with microscopy for high spatial resolution. In contrast to classical B-ETs, molecular optical biosensors have been essential in basic research in the field of taste, but they have not yet been considered for the applications typical for B-ETs. This contribution reviews the use of molecular optical biosensors as tools in taste research and proposes their integration into the concept of B-ETs. Starting with a summary of the current knowledge on the taste system, the manuscript will systematically address applications of different molecular optical biosensors in the tongue, the central nervous system and in recombinant cell systems. Then, we will speculate on a future use of molecular optical biosensors to novel fields of applied taste research.

2. Taste—Function and Mechanism of Action

The taste system is crucial for feeding and survival as well as to detect and discriminate a large amount of chemical substances in complex environments. The sensation of the five basic taste modalities sweet, bitter, umami, sour and salty, gives essential information on food choice and prepares the body for digestion. Each taste modality has a specific role in body homeostasis and taste receptors (TRs) are also expressed in extraoral tissues, where they mediate non-tasting effects, e.g., in the airway, gastrointestinal tract or heart (reviewed in [11,12,13]). In humans, the sweet taste is the most attractive modality, probably because sugars are associated with calories and energy fuel for the body. Umami, the taste of glutamate, reflects the protein content in food while bitter substances are perceived as unpleasant, which likely reflects a warning signal for toxicity. Salty and acid tastes can be attractive or repulsive, depending on their concentration which is critical for mediating body-fluid maintenance and the acid-base balance [14,15]. For the modalities sweet, umami and bitter, flavors are recognized via highly specialized TRs, while salt and acid sensations utilize the activation of ion channels. From a clinical point of view, understanding the functionality and the complex signaling networks downstream of these receptors and ion channels is a major goal, to treat e.g., obesity, diabetes or cardiovascular dysfunctions. On another note, the development of bitter inhibitors may help to improve palatability of unpleasant bitter medicines. For example, special formulations for children are often sweetened although this still does not completely eliminate the bitterness of many drugs [16,17]. Finally, food industries are highly interested in understanding taste physiology to optimize their products with new flavors or substitutes [18,19].

2.1. Taste System Anatomy and Transduction in the Periphery

Taste buds are the peripheral organs of gustation. They are implanted in the epithelia of the tongue, palate and epiglottis [20]. In human beings, ~5000 taste buds are distributed on the tongue and are organized in taste papillae (Figure 1) [21,22]. Fungiform papillae are found in the anterior two thirds of the tongue, they contain ~3.5 taste buds each and are innervated by the chorda tympani nerve. Foliate papillae reside on the posterior lateral sides of the tongue. They contain multiple taste buds and are innervated by both, the corda tympani and the cranial nerve IX, which belongs to the glossopharyngeal nerve [22,23]. Circumvallate papillae on the dorsal tongue are the largest papillae with ~250 taste buds. They are only present in mammals [24] and are innervated by the glossopharyngeal nerve [25].
Each taste bud contains 80–100 mature polarized neuroepithelial taste cells of elongated shape. They are grouped into three categories (Figure 1) [15,20,26]. Type I cells are the most abundant cells and believed to have a glia-like function. They synthesize NTPDase to degrade ATP released by other cells for intercellular communication [15,26,27,28]. Type I cells show an electron-dense cytoplasm, apical dark granules and long microvilli. Conversely, type II cells contain a more electron-lucent cytoplasm and their microvilli are shorter and thicker [29,30]. They are also called “receptor cells” as they express G-protein coupled TRs, which are key players in the transduction of sweet, bitter and umami taste. In addition, type II cells express voltage-gated Na+ and K+ channels to mediate action potentials [15]. Upon depolarization, hemichannels in type II cells allow the release of ATP to stimulate nerve terminals and type III cells [31,32,33,34,35]. The latter are also termed “presynaptic cells” as they synapse with afferent nerve terminals and release serotonin [36,37,38] as well as other neurotransmitters [39,40,41,42]. Furthermore, type III cells are involved in sour taste transduction [43]. They display an intermediate electron density and a single microvillus [29,30]. As the life span of all taste cells is limited to only ~10 days, they need to be replenished regularly. To this end, progenitor cells, also called type IV cells, reside on the basement of the taste bud and give constantly rise to new mature taste cells [15,26,44].

2.1.1. Taste Transduction of Saltiness

Saltiness is associated with the taste of table salt (NaCl) and Na+ ions [45]. At low concentrations, salt is attractive, while at higher concentrations it is aversive [46]. Apparently, different taste cell types and mechanisms are responsible for these responses. The attractive pathway is selective and sensitive to low concentrations of Na+ (10 mM–150 mM) and mediated by amiloride-sensitive Na+ channels (ENaC) [47,48]. The exact channel composition, the downstream signaling, and the cells expressing ENaC are still under debate [49,50,51]. The amiloride-sensitive pathway plays only a minor role in taste perception in humans, with large variability among subjects [51,52]. The amiloride-insensitive aversive pathway responds to a wide range of salts. It is activated only by higher salt concentrations and mediated by a different but still undefined cell population (Figure 2) [46]. Two mechanisms for amiloride-insensitive salt sensation were proposed. First, the vanilloid receptor (V1R) is a candidate [53,54], since mice lacking V1R showed altered nerve responses to salt [53]. Second, an unknown Cl conductance was found to mediate a Ca2+ rise in type II cells in response to high salt concentrations [55].

2.1.2. Taste Transduction of Sour

Sour taste mediates both attractive and aversive behaviors depending on tastant concentration, context (for example presence of sugars) and learning. It is mediated either by organic or mineral acids. Organic acids are sensed by presynaptic type III cells upon changes in intracellular pH [56,57] which induces serotonin release [56]. Such weak acids might permeate the cell membrane in the protonated form [58], dissociate in the cytoplasm and protons may then block Kir2.1 channels, resulting in depolarization and voltage-gated Ca2+ entry [59]. For the sensation of mineral strong acids, a variety of mechanisms have been discussed (Figure 2) [60,61,62,63,64,65] (reviewed in [25,58]). One candidate was the polycystic-kidney-disease-like ion channel (PKD2L1). However, while selective ablation of PKDL1 expressing cells eliminated gustatory neural response [66,67], sour sensation remained intact in PKD2L1 knockout mice [68]. Recently, a new mechanism has been proposed: extracellular protons derived from the dissociation of strong mineral acids might enter type III cells via Otop1, a specific ion channel now termed “sour receptor” (Figure 2). However, despite a large reduction in nerve response to strong acids, Otop1 knockout mice have a retained acid aversion [69]. Therefore, the mechanism leading to the acid-induced avoidance behavior remains elusive, and further transduction pathways may be involved. Furthermore, sour taste may utilize different pathways depending on the species [60,61,62,63].

2.1.3. Taste Transduction of Bitter

In humans, bitter taste is mediated via ~25 bitter taste receptors (T2Rs), which can be co-expressed in different combinations in type II cells [70,71]. Many structurally unrelated compounds are able to activate T2Rs, and while some bitter compounds are specific for one receptor, others can activate more than one [47,72,73]. Studies on native rat receptor cells suggest cellular specificity for certain bitter compounds [74]. T2Rs are G-protein coupled receptors (GPCR) [71,75], mainly linked to a specific taste G-protein named “gustducin” (Figure 2). Even if other G-proteins may be co-expressed in receptor cells, gustducin is the main G-protein involved in bitter transduction [76,77,78]. Upon stimulation of T2Rs, the βγ-subunit of gustducin is believed to stimulate phospholipase Cβ2 (PLCβ2) to mediate Ca2+ release from intracellular stores via inositol-3-phosphate (IP3) [79]. Subsequently, cell depolarization is thought to be mediated by Ca2+-activated transient receptor potential M5 channels (TRPM5) [80], which leads to ATP release via pannexin or CAHLM channels followed by stimulation of afferent fibers and presynaptic type III cells [25,81,82]. In addition, the α-subunit of gustducin was found to activate a phosphodiesterase (PDE) to keep intracellular cAMP levels low and to avoid the activation of protein kinase A, which in turn inhibits PLCβ2 [43].

2.1.4. Taste Transduction of Sweet

Sweet taste is mediated by caloric sugars and artificial sweeteners upon binding to the sweet receptor which is composed of the T1R2-T1R3 heterodimer (Figure 2) [83,84,85]. Receptor cells sensing sweet and bitter compounds are segregated in two different populations [22]. Sweet-sensing cells use the classical bitter downstream signaling involving PLCβ2, IP3, Ca2+ release, TRPM5 and ATP release (Figure 2) [43,83]. However, there might be an alternative transduction pathway for sweet, as T1R3 knockout mice showed residual responsiveness to sugars, but not to artificial sweeteners [86]. This may be mediated by glucose transporters (GLUT and SGLT) and downstream KATP channels [87]. Additionally, before the discovery of the sweet taste receptor, it was proposed that sugars activate adenyl-cyclase (AC) to increase cAMP levels, favoring protein kinase A (PKA) mediated inhibition of K+ conductance resulting in cell depolarization (Figure 2) [43,88,89,90,91,92]. It is discussed, that this pathway is mostly utilized by sugars while artificial sweeteners may largely activate the classical PLCβ2 / IP3 pathway [43].

2.1.5. Taste Transduction of Umami and Additional Taste Qualities

Umami is associated with L-glutamate and guaninmonophosphate/inosinmonophosphate which are produced after hydrolysis of proteins and NTPs [15,45]. As sweet, also umami is sensed by type II cells via T1R1-T1R3 heterodimers (Figure 2) [93,94]. The downstream signaling of umami taste is thought to be similar to that of bitter taste [95].
Carbonation has been recently recognized as an additional taste modality. In type III cells, CO2 is sensed by carbonic anhydrase 4 (CA4) which produces protons and bicarbonate ions. Proton influx into acid-sensing cells is believed to serve for signal transduction of carbonation [66,96].
Dietary lipids are perceived via GPR120 and CD36 receptors that activate a phospholipase A2 which was reported to trigger Ca2+ release from the store and Ca2+ entry via multiple store-operated Ca2+ channels such as Orai1 and 3 [97,98].
Kokumi, the sensation of mouthfullness, is produced by substances that have no taste on their own but enhance other modalities. It is responsible to inform the organism about the presence of amino acids and proteins. Accordingly, it is activated by small peptides, amino acids and Ca2+. Indeed, the calcium sensing receptor (CaSR) is believed to be responsible in this context. CaSR is present in type II and III cells, but not co-expressed with sweet receptors [99,100].
Capsaicin and vanillin evoke a burning sensation when ingested due to binding to V1R, located in the nerve terminals [101,102]. It is debated, whether a variant of V1R is also present in taste cells. V1R was shown to be responsible for capsaicin response in taste receptor cells and to contribute, via capacitative Ca2+ entry, to Ca2+ homeostasis together with mitochondria and Ca2+ exchangers [103]. Furthermore, it was also proposed to account for amiloride-insensitive salt responses in rat [53].

2.1.6. Communication of Taste Cells

To stimulate the nerves and to communicate with each other, taste bud cells release different neurotransmitters and paracrine molecules. Type I cells may also release some neurotransmitters such as GABA [104], however one of their major roles is rather the clearance of ATP by released NTPDase (Figure 1) [26]. Type II cells stimulate the nerves by ATP release (Figure 2) [33,34]. Accordingly, nerve terminals express purinergic receptors (Figure 2) [31]. In addition, ATP also stimulates presynaptic type III cells and exerts a positive autocrine feedback on type II cells (Figure 1) [105], which express M3 muscarinic receptors and release acetylcholine to generate positive autocrine and paracrine signals [42,106,107,108]. Type III cells make synaptic contacts with afferent fibers and release serotonin (Figure 2) [36], noradrenaline [39] and GABA [40]. While Serotonin and GABA act not only on nerve terminals, but have also inhibitory functions on type II cells, the role of noradrenaline is not well understood [43]. Molecules involved in the different signaling pathways can be used as markers to identify the different cell types in a taste bud. Thus, type I cells are recognized by expression of NTPDase [109], and GLAST [110], type II cells by gustducin [79,111], TRPM5 [112,113], IP3R [50] and PLCβ2 [33,49], while type III cells mainly express GAD1 [42,114] or SNAP25 [49]. Additionally, it is possible to discriminate between type II and type III cells according to their response to KCl-mediated depolarization, which induces Ca2+ entry via voltage-gated Ca2+ channels only in type III cells [49,50].

2.2. In Search of an Appropriate System to Study Taste Signaling with Biosensors

Much progress in our knowledge about taste has been achieved in the last decades. However, major obstacles have still not been solved and hamper further research. The main challenge is the absence of a reliable, functionally complete test system to study human taste (reviewed in [24]). So far, taste has been predominantly studied in animals due to limited accessibility to human samples. However, interspecies differences have been widely recognized. For example, taste nerve activity results in different outcomes for carnivores and herbivores when stimulated with salts such as NaCl or KCl [115]. Additionally, the number of TRs is variable among species, e.g., while frogs express 49 bitter receptors (T2R), the numbers for chicken, dogs, cows and humans are 3, 15, 18 and 25, respectively [116,117,118]. Other species, such as domestic cats, lack sweet taste receptors altogether and thus are not attracted by sweetness [119]. Even the shape of taste buds differs: while humans contain oval taste buds, they are spindle-like in pigs or melon-shaped in horses [24]. Most of the research on taste has been performed on rodents. However, the sweet receptor, which was identified first in rat [83] and then in humans [93], displays structural and functional differences between the two species, as the selective competitive inhibitor lactisol and the artificial sweetener aspartame are effective only in humans [120,121]. Furthermore, while rodents are strongly attracted by polysaccharides derived from starch, humans are not [122,123].
An alternative to primary rodent tissue is the use of cell lines expressing heterologous functional gustatory receptors together with molecules essential for the signal transduction (Figure 3). These recombinant expression systems can be used for high throughput screenings of a large number of chemicals but sometimes the results might not be representative of the situation in vivo, as they lack the complexity of native tissues. To study human taste, it would be best to have access to human samples. In principle, this is possible, since papillae can be donated as they regenerate [124]. However, even when donors were found, papillae are naturally composed of mixed cell populations, which have a limited life span. Indeed, up to now primary human taste cells can be maximally cultured for seven passages [125] and heterogeneity and variability of the samples are critical. To overcome these limitations, immortalization of human taste cells yielded a test system able to reliably sense bitter substances [117]. Alternatively, isolated and immortalized progenitor taste cells could be used to differentiate into mature taste cells or to build organoids [126,127]. However, the knowledge on how to differentiate these progenitors is still at the beginning [128] and nobody has so far attempted to isolate, cultivate and differentiate human progenitors cells. The different biological models that have been used and analyzed with optical biosensors to progress in the study of taste physiology up to now can be grouped into four main categories as follows (Figure 3):
  • Isolated animal primary taste cells, taste buds, tongue epithelia and slices were used in combination with fluorescent dyes in ex vivo live imaging experiments for unravelling the intracellular signal transduction pathways and intercellular communication.
  • Recombinant systems expressing taste receptors and downstream signaling molecules in non-taste cell lines were employed upon loading with chemical dyes in plate reader experiments to study receptor structure, binding sites, selectivity and sensitivity in high throughput.
  • Biosensor cells expressing specific neurotransmitter/hormone receptors were used upon loading with fluorescent dyes and juxtaposed to taste cells/tissue to monitor with live imaging experiments the release of neurotransmitters such as ATP, serotonin, noradrenaline, GABA and acetylcholine.
  • Expression of genetically encoded biosensors in neurons of mice to monitor brain activity patterns in response to flavor application in vivo and to label specific cell types in a reporter gene mode.

3. Use of Molecular Optical Biosensors for Taste Research

In the following paragraphs, the application of different molecular optical biosensors for the study of taste sensation will be systematically reviewed according to their use in taste buds and the central nervous system (CNS).

3.1. Application of Molecular Optical Biosensors for Peripheral Processing of Taste

In contrast to artificial taste sensors, devices or recombinant cells, native taste cells detect tastants with a much higher performance and in a physiological context [129]. In search of taste transduction molecules, primary cells isolated from taste buds or lingual slices of animals are thus an indispensable tool. Due to limited accessibility of human samples, these approaches mainly used rodent tissue. However, as taste transduction displays differences between species, our knowledge about human taste physiology, even at the level of primary signal transduction, is still incomplete. Studies on taste signaling were mainly achieved using either dissociated primary taste cells or lingual slices containing taste buds. In both cases, these samples are derived from an acute isolation procedure and could be used only for a few hours. As a readout for sweet, bitter, umami, salty and sour responses mostly fluorescent chemical Ca2+ sensors were used. For sour and salty taste, also pH fluorescent indicators were used (Figure 3, Table 1).

3.1.1. Chemical Ca2+ Sensors

Fluorescent biosensors of divalent metal ions were first discovered by Tsien in the 1980s [130,131,132]. They are commercially available and allow live cell imaging studies upon easy loading protocols. In the field of taste research, Ca2+ sensor dyes are preferentially used among ion indicators and have promoted the discovery of main signaling mechanisms (Table 1). A pioneering study used the Ca2+ indicator Fura-2 in rat taste cells to prove that bitter substances induce Ca2+ release from internal stores [133], and this was confirmed in mudpuppy [134]. Fura-2 is a dual excitation single emission Ca2+ indicator whose excitation spectra shifts from a wavelength of ~380 to ~340 nm upon Ca2+ binding. Therefore, the ratio of the emissions at those two wavelengths is directly related to the amount of intracellular Ca2+ [135], offering the advantage of an internal calibration and relative robustness against uneven dye loading or sample thickness, variable wavelength and intensity of excitation light, dye leakage and photobleaching [130]. With a Ca2+ dissociation constant (Kd) of 140–230 nM, Fura-2 is ideally suited to detect physiological cytosolic Ca2+ concentrations [130]. Fura-2 requires ~10–40 min to permeate into the cells. To reduce accumulation in organelles, it is often used in combination with sulfinpyrazone, a blocker of the organic anion transport system [136]. To further improve loading and retention inside the cells, the derivative Fura-2-acetoxymethyl ester (Fura-2-AM) was developed [137]. The non-polar ester permeates the plasma membrane, and the ester bonds are then cleaved by cytosolic esterases, leading to a trapping of the polar dye inside the cell [131]. To inhibit extrusion from cells via multidrug resistance transporters (MDR1), as observed for Fura-2-AM in rat vallate papilla cells, substrates and/or inhibitors of MDR1, such as verapamil, tamoxifen and cyclosporin A can be used [138]. Efficient Fura-2 loading protocols of both, dissociated cells and taste buds, were developed [37,139,140,141,142,143,144]. In combination with conventional and confocal microscopic live imaging, these were used to unravel the Ca2+ responses of sweet, umami, bitter, salty, sour, fatty acid and kokumi taste in mice (Table 1). Furthermore, these experiments revealed mechanisms important for Ca2+ homeostasis in taste cells and for unconventional Ca2+ entry. For example, store-operated Ca2+ channels (SOC) were found to be crucial for fatty acid and bitter-mediated signaling [97]. Mitochondria and sodium-calcium exchangers (NCXs) were shown to control basal cytosolic Ca2+ levels [145]. In addition, Fura-2-based experiments helped to solve the debate whether VGCCs are involved in Ca2+ entry in type II cells. Generally, it was believed that only type III cells possess VGCCs [113,146]. However, with the use of Fura-2, some type II cells were described to utilize a different pathway than PLCβ2/IP3 in response to bitter compounds and to display voltage-gated Ca2+ entry [103]. Fura-2-based experiments revealed the modulation of taste signaling by neurotransmitters and hormones, such as ATP [140,144], serotonin [38], glutamate [143], adrenaline [147] and oxytocin [142]. Application of Fura-2 on taste cells from different species, including mice, rats [133], mudpuppy [148] and humans [98,125] unraveled species-dependent similarities and differences. For example, compared to mammalian taste cells, mudpuppy counterparts showed that prolonged bitter stimulation results not only in Ca2+ release from stores but also in Ca2+ influx [148]. Fura-2 was also used in live imaging experiments in cells derived from a taste 3D culture [127].
Thanks to its short wavelength spectrum, Fura-2 can be combined with green fluorescent proteins (GFP) and yellow fluorescent proteins (YFP) to label specific cell populations (see Section 6) [38,42,113,141,143,149,150]. This has facilitated the discovery of functional differences between receptor and presynaptic cells in terms of Ca2+ signaling: as mentioned above, for type II cells the major Ca2+ source is the endoplasmic reticulum, while in type III cells Ca2+ enters via voltage-gated Ca2+ channels. Further, Fura-2 was used in combination with the Na+-sensitive dye AsanteNaTrump-2 to simultaneously measure Ca2+ and Na+ changes in response to the activation of TRMP5 and TRPM4 channels by sweet and bitter compounds [151]. The interplay between intracellular acidification and Ca2+ signals was investigated by live cell imaging experiments measuring at the same time H+ with the pH-sensitive dye pHrodo-Red and Ca2+ with Fura-2 [69]. Fura-2 can be further combined with the ratiometric voltage-sensitive dye di-8-ANEPPS although this is not optimal (see Section 4.1) [152]. Fura is also available in a red version (Fura-red) which is excited at 605–700 nm, and when combined with the Ca2+ dye Fluo-4 can be used for ratiometric measurements, in order to correct for changes in focal plane which may occur during imaging [153,154].
Besides ratiometric Ca2+ dyes such as Fura-2, also single wavelength indicators have been used. They are very bright and can be easily combined with other fluorophores without spectral overlap [155]. These dyes do not shift their excitation or emission spectra upon Ca2+ fluctuations, but change in fluorescence intensity according to the intracellular Ca2+ concentration. Thus, single wavelength indicators require excitation with only one wavelength and the time intervals between two subsequent image acquisitions is reduced. This is of importance for live cell imaging experiments, especially when measuring fast Ca2+ changes such as voltage-gated Ca2+ currents generated by action potentials. A disadvantage of single wavelength indicators is that dye loading may differ between cells, compromising a correct Ca2+ quantification. Thus, these cells cannot be directly compared in terms of Ca2+ levels and each individual cell has to be normalized to its background fluorescence [135]. Amongst the single wavelength indicators, fluo-dyes belong to the family of high affinity Ca2+ indicators with a Kd of 390 nM [155]. In Ca2+-uncaging experiments with Np-EGTA-AM, Fluo-4 served to clarify the presence of Cl conductance activated by Ca2+ in taste cells [156]. In addition, fluo-dyes have been largely used in recombinant HEK cells where Ca2+ transients in response to taste stimulation were predominantly analyzed with plate reader-based bulk measurements (see Table 1 and Table 3, and Section 5).
Due to their high quantum yield and low toxicity, Calcium Green-1 (CaG; X 490 nm, M 530 nm) and Calcium Orange (CaO; X 549 nm, M 576 nm) are preferred single wavelength indicators for live Ca2+ imaging of intact taste tissues. The Kd of CaG is ~190 nM and upon Ca2+ binding its fluorescence emission increases up to ~100-fold [155]. In its dextran-conjugated form (CaGD) it is not membrane permeable but has to be applied invasively with a patch pipette [135]. However, once inside the cells, dextran conjugates are retained for long periods and even tissue slicing and cell dissociation do not affect their intracellular concentration. Thus, specific CaGD and CaOD loading protocols were established in the taste field [33,157,158] which allow to specifically label the apical, differentiated taste cells, while basal progenitor cells remained dark. In this way, individual taste cells, their cell bodies and both apical and basal processes could be readily distinguished. This was ideal for studying taste sensation, since differentiated type II and type III cells are the cells responding to tastants with Ca2+ signals. Furthermore, this approach permitted to study taste cells in the intact taste bud with apical and baso-lateral polarity for exposure to stimuli in a physiological way [42]. Since desensitization is an issue in primary taste perception, it was also important that stimuli could be applied at slow or fast time scales, i.e., either as bath perfusion or by pressure injection [42,47,102]. Confocal microscopy for live imaging from individual cells was adopted to study Ca2+ responses to umami [157], bitter [74,159], kokumi [100], sour [56,59,160] as well as sweet and salty compounds [161]. Furthermore, to enable in situ two-photon live imaging, CaGD-soaked paper was placed on the tongues of anesthetized mice and uniform electrical pulses were applied with a tweezer type electrode to the tongue surface. Intravital two-photon microscopy was then performed on the tongue firmly positioned in a custom-made chamber. This allowed to visualize taste responses upon application of small molecules on the tongue as well as upon their entry into blood circulation, suggesting that small molecules can diffuse through tight junctions to reach microvilli from below to stimulate taste receptor cells in an indirect manner and not only through the taste bud pore [77]. Although CaOD has been reported to be more difficult to load than CaGD and to be poor in performance [59,162], it was used when the green channel was employed for other markers such as in transgenic mice expressing GFP under specific promoters [33,42,49,59,114]. Additionally, CaO was used in combination with the pH-sensitive dye BCECF-D to simultaneously measure pH and Ca2+ changes in intact lingual preparations upon focal stimulation [59,163].

3.1.2. Genetically Encoded Ca2+ Indicators (GECIs)

A main disadvantage of synthetic Ca2+ sensors is their lack of control over loading into specific cell types and subcellular localization. Thus, synthetic dyes sometimes do not enter the cells of interest or they tent to compartmentalize in the endoplasmic reticulum or other compartments [173]. In contrast, genetically encoded Ca2+ indicators (GECIs) allow cell-type and subcellular targeting specificity [174,175]. Most GECIs do not contain synthetic compounds or cofactors and are not extruded by the cells. They are mostly fluorescent proteins that change their emission/excitation spectra upon Ca2+ binding inside the cells. Synthesis and expression of GECIs occurs upon introduction of genetic expression elements into target cells [174]. GECIs have been engineered after the discovery of aequorin and GFP, both derived from the jellyfish, Aequorea victoria [175,176,177,178]. Currently, most genetically encoded biosensors use spectral variants of GFP (XFP) with improved optical properties or siblings of GFP from other cnidarian species [174]. Considering the advantages of GECIs, such as the possibility to target them to a specific cell population and even to subcellular compartments, it is surprising they have never been used to transduce primary taste cells. Maybe, one reason is that the expression of recombinant proteins might require some days and this has to fit into the short life span of taste cells of ~10 days. However, a recent approach using expression of a G-GECO Ca2+ sensor in 3D cultures of an immortalized human tongue cell line showed measurements of acute Ca2+ changes with confocal and light-sheet fluorescence microscopy upon tastants perfusion [179]. Furthermore, cell-type specific expression of GECIs followed by in situ microscopy was realized in a few studies [55,180,181]. Amongst these, Roebber et al., used Pirt-GCaMP3 mice where the Ca2+ sensor is expressed in sensory neurons as well as in type II and type III cells, thus this approach is well suited to investigate salt detection in tongue slices [55]. Apart from this, genetically encoded sensors were mostly used to study the decoding of taste sensation in the CNS (see Section 3.2).

3.1.3. Molecular pH Biosensors

While Ca2+ is the main effector of taste signaling in general, the study of sourness also needs measurements of proton concentrations both in the extracellular milieu and in the cytoplasm (Table 1). Furthermore, the responses to acids are dependent on acid strength, with weak organic acids, such as citric and acetic acids, paradoxically inducing a stronger response [59]. Thus, the ideal setup for analysis of sour taste signal transduction uses contemporary measurements of Ca2+ and protons. While Ca2+ transients are rapid and Ca2+ concentration can increase up to 100 times, the intracellular pH, usually only varies between 6.8 and 7.4 in the cytosol and variations have longer time scales. To quantitatively measure pH, the pKa of the indicator must match the pH of the milieu. Mostly, the dyes pHrodo-Red [66,67], and BCECF [59,163], in their permeant AM form were used as pH indicators in the taste field. BCECF (2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein) is a polar derivative of fluorescein introduced by the “three witches” Rink, Tsien and Pozzan in 1982 [182]. The pKa of BCECF of 6.98 makes it suitable to measure intracellular pH changes and its emission fluorescence intensity decreases with acidification. With rare exceptions [59], BCECF is usually applied as a ratiometric dye, as measuring the emission upon excitation at its isosbestic point (440 nm) and the maximum (490 nM) allows to correct for concentration, pathlength, leakage and photobleaching [66,164,183]. In contrast, the fluorescence intensity of the single wavelength indicator pHrodo-Red (pKa of 6.5) increases with acidification and its excitation/emission maxima (560/585 nm) render it suitable for multiplexing with fluorophores such as GFP. Quantification of intracellular pH is possible for both, pHrodo-Red and BCECF, upon calibration with nigerin [164]. In the dextran and AM forms, BCECF is suitable for iontophoretic loading of the lingual epithelium. To simultaneously investigate pH and Ca2+ changes in the very same cell in response to sour stimuli, BCECF was applied together with CaOD [59,163]. Confocal microscopy upon focal application of sour stimuli to the taste pore with a puffer pipette allowed to precisely determine the exact concentration of the acid reaching the taste pore region by adding to the stimulus solution the dye lucifer yellow CH, which is pH-insensitive and not cell-permeant [59,163]. It was determined, that the acids reaching the taste pore were able to acidify most of the taste bud cells, but only a subset of them (25 %) showed concentration-dependent Ca2+ responses [59,163] at concentrations similar to the sensitivity for citric acid and HCl in mice [184]. This also demonstrated that sour-induced Ca2+ transients occur only in type III cells and are mediated by Ca2+ entry via voltage-gated Ca2+ channels. Furthermore, a linear relationship between intracellular acidification and Ca2+ response, but not with the extracellular pH, was shown. At equal acidity, weak acids (undissociated: citric, acetic acid, with higher pKa) were a much more potent stimuli than strong acids (dissociated: HCl, with lower pKa) [59,163]. As mentioned earlier, the non-linear relationship between extracellular and intracellular pH may be explained by separate pathways for weak and strong acids, with the second involving the entry of protons through the Otop1 channel [69]. Recently, this hypothesis was confirmed with simultaneous live imaging of pHrodo-Red, Fura-2 and YFP in PDK2L1-YFP reporter mice [66,67]. This revealed both intracellular acidification by acetic acid and Otop1-mediated proton influx by HCl, the latter with a lower onset and offset compared to acid diffusion. Similarly, pHrodo-Red proved that Otop1 channels mediate intracellular acidification upon lowering the extracellular pH in a recombinant cell model [185].

3.2. Biosensors to Study Taste Representation in the Central Nervous System

While primary taste signal transduction occurs in taste buds, their responses are transferred to the brain, where they are processed and converted into an internal representation of taste (Figure 1). In the brain the information is processed and passed by several relaying structures, to terminate in the cortex where all the information about palatability (taste quality), reward (hedonic value) and energy source (metabolic information) are integrated to take a decision about food ingestion. Other sensations, including chemesthesis as well as sight and hearing play also an important role in the interpretation of food value and influence our behavior.
Sensory neurons innervating taste buds have their cell body in the geniculate, petrosal and nodose ganglia and synapse with neurons of the nucleus of solitary tract (NTS) in the brain stem (Figure 1) [186]. These project to the parvicellular portion of the ventroposteromedial nucleus of the thalamus [187]. From there, the information travels to the primary gustatory cortex in a region called “insula”, where the neurons respond to taste stimuli as well as to visual, auditory and tactile cues to decode the qualities of food. In humans, the information passes then to the orbitofrontal cortex, which contributes to perception of tastants, pleasantness of food and decision making about food ingestion [188,189]. In the field of taste neuroscience, a principal question is how signals are decoded at the different levels. Currently, mainly three hypotheses are being discussed. First, the “labelled-line coding” theory proposes that taste cells and neurons are tuned to respond only to a single taste modality and use dedicated neural channels. Second, the “combinatorial-coding” theory suggests that stimuli are decoded by the contemporary activity of a particular ensemble of neurons. Third, each neuron may respond to diverse flavor categories using a “temporal-coding” of action potential firing (reviewed in [81,190]). It is believed that from the periphery to the central nervous system (CNS), there is an increasing complexity of taste code processing, suggesting a preference for labelled-line coding at the level of taste buds and sensory fibers and for combinatorial and temporal-coding involving functional neuronal ensembles in the higher structures (for review [20,191]). While topographic mapping of specific taste qualities to dedicated brain regions was neglected [192], this view was challenged by experiments in mice showing that neurons coding for one taste quality are anatomically clustered [193] and by a magnetic resonance study in humans, which demonstrated that the different taste categories are represented in discrete regions of the insula [194,195]. All these theories were developed based on electrophysiological or optical recordings in living animals (reviewed in [187,196,197]).
A lack in spatial or temporal resolution inherent to the aforementioned approaches was overcome with the use of in vivo microscopy of genetically encoded biosensors as these combine high spatial and temporal resolution. This technique allowed the generation of taste stimulus profiles by localizing individual neurons and quantifying their Ca2+ changes, which correlate with the firing of action potentials (Table 2) (reviewed in [198]). The two major technical challenges of such an approach are: (1) genetic targeting of a specific neuronal population, and (2) real-time imaging in brain regions in living animals (Table 2). To address the first point, targeting of genetically encoded biosensors to defined cell populations can be done by stereotactic injection of viral biosensor carriers. Amongst these, Adeno-associated viruses are attractive to induce long-term stable transgene expression in the cells of the CNS with high efficiency and without side effects [199]. They mediate cellular specificity via serotype [200]. Alternatively, transgenic mice using cell-type specific promoters can be generated to express a GECI in the target neuronal population (Figure 3). But a major challenge here is the identification of specific promoters. For example, in one study, 40 transgenic mouse lines were made and screened to efficiently and selectively drive GCaMP3 expression by the promoter Thy1 [201]. The alternative strategy was to drive GCaMP3 expression in the soma of geniculate ganglia neurons by stereotactic injection of a viral construct in the brainstem. To perform live Ca2+ imaging with good spatial and temporal resolution in the ganglia, which are buried in a bony structure, a micro-endoscope was positioned directly into the tissue [201]. As for the second challenge, next-generation Ca2+ sensors, such as GCaMP6, detected single action potentials in vivo with high reliability [202]. Upon opening of the skull via surgery to generate an optical imaging window, Ca2+ changes were measured in vivo mainly via two-photon microscopy. The latter features low phototoxicity and reduced light scattering and thus permits imaging up to a depth of few millimeters (reviewed in [203,204]) and to record Ca2+ changes in real-time at cellular resolution with fields of view of 200–500 µm2 [205].
To correctly identify the anatomical structure of interest in the brain, additional tracing experiments are often required. For this purpose, virus particles encoding fluorescent proteins (GFP, DTomato, mCherry or tWGA-DsRed) or dextran-conjugated dyes (MicroRuby dextran) can be injected in structures that send innervation to the selected brain region (anterograde tracing) or receive innervation from them (retrograde tracing) (Table 2) [192,193,206,207]. For example, upon expression in type II cells, the tracer tWGA-DsRed was transferred to neurons via trans-synaptic transfer and revealed that sweet and bitter taste have distinct topographic representation in the NTS [206]. Similar approaches were used to delineate the projections from the gustatory cortex to the amygdala [207], or from the thalamus to the gustatory cortex [192,207]. Another way to trace neurons activated by gustatory stimuli, is to analyze the expression of early genes like c-fos or Zif268 [206,208]. However, this cannot be performed in living mice and has so far involved extensive sectioning and computational reconstruction of 3D images. Recently published methods of optical tissue clearing allow to avoid sectioning, since they render the brain transparent to visualize the tissue in toto by direct 3D imaging [209]. Finally, besides purely descriptive analysis of circuitries, novel optogenetic approaches additionally permit to delete functional connections selectively via targeted diphtheria-toxin expression in freely behaving animals. This approach was used to characterize the role of SatB2 neurons of the parabrachial nucleus in gustatory sensation [208]. SatB2 was found to be a selective marker of sweet-sensitive neurons and upon their ablation in transgenic mice, the sweet taste sensation was severely impaired, while the other taste sensations remained intact. Furthermore, using a miniaturized microscope to observe SatB2-positive neurons expressing the GECI GCaMP6s it was possible to visualize the activity of sweet responding neurons in awake animals during licking behavior. This showed that neuronal activity was synchronized with licking. The expression in SatB2-positive neurons of channelrhodopsin, a light-activated Na+ channel regularly employed in optogenetic settings, allowed the specific photostimulation of SatB2-positive neurons and induced a licking behavior similar to that of sweet substances, even when water was presented. This suggested that these mice sensed the sweet taste upon optogenetic stimulation of SatB2-positive neurons, even if the taste buds were not involved [208]. Such complex experiments are important to unravel the central mechanisms of gustatory sense (reviewed in [210,211,212]).

4. Additional Optical Biosensors in the Taste Field

4.1. Voltage-Sensitive Dyes

Although of their tongue-epithelial origin, taste cells possess electrical characteristics comparable to those of neurons [214]. Patch-clamp recordings showed that mammalian taste cells are electrically excitable and can fire action potentials (AP) [215,216] in response to sweet [217], salty [218], sour [63] and bitter compounds [219]. In rodents, voltage-gated Na+ and Ca2+ currents are involved in depolarization, whereas K+ and probably Cl currents participate in repolarization during an AP. Type II and type III cells differ in the density and kinetics of Na+ and K+ currents and in the duration of APs [146,220,221,222]. Since different stimuli evoke distinct patterns of AP firing, these are likely to play a role in taste quality coding [223] and the regulation of neurotransmitter release [214]. Furthermore, the firing activity of taste cells seems to be correlated with that of nerve fibers, and to depend on taste modalities [224].
Alternative to patch-clamp studies targeting only a single cell, the electrical activity of multiple cells can also be measured with voltage-sensitive dyes, which have been in use since the 1970s [225]. Their fluorescence changes depend on membrane potential specifically at the plasma membrane [226]. At difference with Ca2+ indicators, they have a time resolution in the few milliseconds range, they can measure also subthreshold events and can be used in cells lacking depolarization-induced Ca2+ changes [226,227,228]. However, voltage dyes are often less bright, requiring stronger illumination which may lead to photobleaching and phototoxicity [226]. Despite their advantages, voltage-sensitive dyes have been rarely used in the field of taste research. Therefore, it is still largely unknown how voltage changes in taste cells are transduced in Ca2+ signals, neurotransmitter release and communication with the afferent fibers. Among the voltage-sensitive dyes, analogues of aminonaphthylethenylpyridinium (ANEP) [229,230] have been the most popular. They fluoresce when incorporated in the cell membrane and can be applied as retrograde tracer of neuronal pathways [231]. ANEPs are “fast potentiometric dyes”, where changes in the electric field affect the electronic molecule structure, resulting in a shifted excitation spectrum [232]. ANEPs can therefore be used to measure membrane potential by dual wavelength ratiometric methods [233,234]. They show a linear electrochemical response to membrane potential changes from −100 mV to +100 mV [230,235] with response times of few milliseconds and they are easily incorporated in the cell membrane upon short incubation [160]. During the first 15–30 min after incubation, the dye response is unstable and can strongly fluctuate in both directions [152]. Quantification of ANEP signals are achieved by ratiometric measurements using blue (450 nm) and cyan (505 nm) excitation [233,234]. In combination with Fura-2, ANEP-based measurements showed that glutamate-induced Ca2+ transients in taste cells occur via two mechanisms, of which only one involved cell depolarization [152]. Another study used ANEP to investigate depolarizing potentials in acid-sensitive cells in combination with CaGD and BCECF for the measurements of Ca2+ and pH, respectively [160]. Since spectral properties precluded simultaneous measurement of all three parameters, they could only conclude that acidification-induced pH decrease, depolarization and Ca2+ changes occur in a subset of cells, but the temporal order and the occurrence in the same cells remained elusive.
Changes in the membrane potential of taste bud cells were optically evaluated with tetramethylrhodamine methyl ester (TMRM), another voltage-sensitive dye. This dye is obtained by esterification of tetramethylrhodamine [236]; it is a lipophilic cation that localizes in the cell membrane of the outer mitochondrial membrane, in proportion to its potential [236,237]. In intact tongue epithelium, taste buds were stained by exposing their basolateral membrane to the TMRM solution, using a special chamber. Comparison of patch-clamp and optical voltage recordings revealed that cells in the taste bud are heterogenous in their voltage responses to a tastant mixture, with some cells undergoing depolarization and others hyperpolarization [238]. At the time when these studies were published, the functional differences between type II and type III cells were not clear yet and many components of the signaling cascade were still to be discovered. It is therefore surprising that no further investigation with voltage-sensitive dyes followed. For example, online voltage measurement in taste cells may help to refine the mechanisms of signal transduction and to link changes in membrane potential to the activation of voltage-gated currents. Additionally, since optical recordings offer the advantage to measure voltage changes in a large cell population, voltage sensors could help to understand the dynamics of cell–cell communication in the taste bud. Furthermore, simultaneous imaging of Ca2+ in taste bud cells and voltage in the nerve fibers may help to understand how kinetics of Ca2+ transients are transduced into defined firing patterns of afferent fibers.
An emerging technology for optical monitoring of voltage dynamics comes with genetically encoded voltage sensors (GEVIs). GEVIs are cell-specific, less invasive, allow long-term recordings of larger cell populations and give additional information about the anatomy of the structures imaged. GEVIs can detect slow subthreshold events as well as repetitive firing of APs, therefore they are suitable to detect neuronal ensembles and synchronized activities. However, GEVIs are still slower compared to the fast voltage-sensitive dyes (ms vs µs). Furthermore, photobleaching and toxicity might be an issue (reviewed in [239,240]), although new GEVIs have improved sensitivity, brightness and kinetics [241]. GEVIs can be used in vitro and in vivo in order to report voltage from dozens of neurons simultaneously [242] and they can be targeted to a specific cell population [243]. Initial versions of GEVIs were fusions of a fluorescent protein and a voltage-sensing domain. Recent designs, such as Ace-mScarlet A, used a bright fluorescent protein with a voltage-sensitive rhodopsin. Thanks to its red-shifted spectrum, Ace-mScarlett can be used together with green emitting GEVIs or GECIs and also with blue-light excitable opsins, allowing flexible and complex experimental configurations suitable to study neuronal circuits [244]. A “chemigenetic” sensor called Voltron was based on Förster resonance energy transfer (FRET) between a rhodopsin and a synthetic dye. Its increased photon yield allows longer in vivo recordings and in ten times more neurons [241]. Despite the large progress in GEVIs synthesis and their increasing applications, they have not yet been applied to study taste transduction in taste buds or in the brain and only few studies report the use of voltage-sensitive indicators to study functional projections between the gustatory cortex and other brain regions [245]. However, further use of GEVIs is largely desired to improve our knowledge about cell–cell communication within the taste bud and coding of taste signals in the brain.

4.2. cAMP Sensors

Besides Ca2+ indicators, also cAMP sensors may be of interest for taste studies as the cAMP/PKA pathway was shown to be involved in bitter, sweet and umami transduction (Figure 2) [43]. Intriguingly, since the discovery of the sweet taste receptor and the PLCβ2/IP3 pathway, cAMP research was largely neglected in taste research. However, in early studies, it was shown that caloric sugars lead to GTP-dependent elevation of cAMP levels. This in turn was proposed to induce PKA-mediated phosphorylation of K+ channels resulting in their closure and cell depolarization [88,89,90,91,92]. This view was later challenged by experiments on gustducin knockout mice, which showed that bitter and umami compounds activate PDEs to keep cAMP levels and PKA activity low in order to allow a permissive condition for the taste-induced Ca2+ signaling (Figure 2) [43,246,247]. Alternatively, it was proposed that cAMP is important to regulate the activity of cyclic nucleotide-gated channels that play a role in regulating membrane potential [248,249]. Since in these studies cAMP was measured with enzyme immunoassay on lysate extract from tongue epithelia, they provided poor temporal and no spatial or cell-type specific information. However, now there are fluorescent molecular cAMP biosensors that allow to study cAMP dynamics in living cells. The first molecular cAMP biosensor was introduced in 1991 [250]. It used fluorescein labelled catalytic- and rhodamine labelled regulatory-subunits of PKA to produce a FRET-based cAMP sensor [250]. However, since the fluorophores are not genetically encoded, FRET-sensors had to be microinjected [251]. In the last 20 years, genetically encoded FRET-based cAMP biosensors were developed and allowed to unravel the relevance of compartmentation of intracellular cAMP signaling. The first genetically encoded cAMP sensor was generated tagging the PKA with two FRET-suited GFP mutants and this was used to monitor cAMP fluctuation in cardiac myocytes [252,253]. Since then, cAMP sensors have been continuously improved including newly discovered cAMP binding sequences and fluorescent proteins (for reviewed see [254]). Furthermore, subcellular targeting of such sensors permits to study changes in cAMP levels in micro- and nanodomains [255] and the genetic approach renders them suitable for studies in recombinant cells lines, primary cells and in vivo [256,257,258]. Therefore, they would be very helpful to define the precise role of cAMP in taste transduction. For example, they could help to understand if natural sugars and synthetic sugars differ in the stimulation of the cAMP pathway [91,92,139] and if sweet, bitter and umami signaling induce diverse cAMP responses.

5. Recombinant Systems to Study Taste Receptor Function

Engineered reporter cell assays systems have been developed and used in the field of taste to characterize the functions and structure of TRs and to find novel agonists and antagonists. In particular, the human embryonic kidney cell line 293 (HEK293) [47,72,259,260,261] and less frequently also Chinese hamster ovary (CHO) [262] cells were used for this purpose (Figure 3, Table 3). Several transduction components of the different taste modalities have been so far expressed in heterologous systems, such as sweet, umami and bitter receptors, but also channels including V1R [261], CaSR [263], and PKD2L1 (Table 3) [154,260,264]. About 20 years back, pioneering studies in this field faced two major challenges: first, the understanding of signaling pathways was still very limited, and second, targeting the receptor proteins to the plasma membrane was not efficient. These problems were addressed by co-expression with the α-subunit of the G-protein gustducin [83,94] and the production of chimeras between the taste receptor and a sequence of rhodopsin [47]. These studies were crucial to understand that T1R2-T1R3 dimers form functional sweet taste receptors [68] and that homomeric T2Rs act as bitter receptors [47]. Furthermore, these studies proved that both sweet [83,94] and bitter [47] receptors require the α-subunit of gustducin to give rise to intracellular Ca2+ signaling via activation of PLCβ2. Further, recombinant systems allowed to identify the structural requirements for bitter receptor activation and agonist interaction [265] and they were used to explain the mechanism of bitter side-taste of synthetic sweeteners: indeed, while acesulfame and saccharin at low concentration are sweet agonists, they become sweet antagonists and activate bitter receptors at higher concentrations [72]. Recombinant systems were also used to study the interaction site of the sweet receptor with the sweet taste inhibitor lactisol [120] or with synthetic sweeteners such as cyclamate [266]. They were also crucial to prove that sweet and umami receptors share the T1R3 subunit [93]. Heterologous systems expressing the transient receptor potential family members PKD1L3 and PKD2L1 were used to investigate whether they may represent the sour taste receptor [150], and recombinant systems were important to prove that TRPM5 opening is induced by intracellular Ca2+ [112,267]. While the most intensely studied taste quality in engineered cell lines is bitterness, reports for salty taste using recombinant systems with optical readouts are lacking.
Since the discovery of the composition of taste receptors, they have been co-expressed with the Gα15 or the artificial chimeric Gα16 subunits of gustducin 44, which efficiently couples Gs, Gq, Gi and gustducin to PLCβ2 [47]. However, since these subunits were derived from murine hematopoietic cells [268,269], the human receptors expressed in the recombinant system did not couple with their native G-protein [270,271]. Furthermore, in native tissue, taste signaling involves also Gαi-2, Gαi-3, Gαs and Gα14 which are often co-expressed with gustducin [272,273,274,275], and recombinant assays may suffer from molecular crowding resulting in false-positive results [19]. These may be reasons why the results obtained in recombinant systems fall short of the situation in vivo, especially for human cells. Nevertheless, the Ca2+ transients induced by the coupling of the recombinant TRs to promiscuous G-proteins can be quantified with synthetic Ca2+ indicators, of which Fura and Fluo are the most preferred for their easy loading protocol and high signal-to-noise-ratio (Table 3). However, as GFP was often used to label transduced cells [47,83,94,259,276], Ca2+ measurements were contaminated by GFP fluorescence [277]. An approach to overcome this problem is to measure Ca2+ changes using red-shifted single wavelength Ca2+ indicators like X-Rhod (X 580 nm, M 602 nm) [262,277]. Alternatively, the labelling of transduced cells could employ other fluorescent protein variants [112]. As recombinant cell lines can be easily expanded and passaged, Fluorescent Imaging Plate Reader (FLIPR) approaches to quantify Ca2+ changes for enhanced throughput screening were developed to perform quantitative optical screening and cell-based kinetic assays [278]. They allow simultaneous fluorescence measurements from entire 96, 384 or 1536 well microplates, with kinetics in the sub-seconds range in combination with precise compound injection and controlled temperature and CO2. However, since FLIPR measurements are at the expense of spatial resolution, additional microscopic imaging is required to get cellular and subcellular resolution (Figure 3) [154,260,264].
Industrial applications in the taste field have largely profited from recombinant models, and different cell-based assays were patented to test bitter, sweet and umami substances (reviewed in [19]). For example, HEK293 cells expressing T1R2-T1R3 receptors where used to discover novel sweet taste enhancers or natural high-intensity sweeteners. A bitter-sensitive reporter cell line expressing T2R44 was used to identify the first synthetic bitter blocker GIV3727 [279]. In addition, recombinant cell lines to find novel ligands for umami (T1R1-T1R3) [93] and kokumi receptors (CaSR) [263] were developed. To study salty taste compounds, HEK293 cells transiently transfected with ENaC were used in combination with ion-sensitive dyes as a measure for membrane potential or sodium [280,281]. Given that the functionality of signaling molecules is sensitive to the cellular environment, there has always been a desire in the taste field to work with primary cells. Indeed, human primary taste cell cultures were developed [98,125] and albeit their limited accessibility and life span, the introduction of foreign genes is possible and new techniques are still under development [282]. For example, α1 adrenergic receptors were expressed in isolated primary taste cells and then stimulated with noradrenaline upon loading with Fura-PE3, which was preferred as it is less prone to leakage and compartmentation [283]. To generate large numbers of human cells for enhanced throughput analysis, an original approach was the immortalization of primary human lingual cells to produce cell lines that endogenously express taste receptors. These were found to express functional bitter receptors as well as naturally occurring downstream signaling components [117]. Additionally, these cells were engineered to stably express a GECI (G-GECO). This prompted the generation of spheroids where Ca2+ signals could be measured in all the regions of a spherical 3D structure, where cell–cell interactions are well preserved [179]. Spheroids can be easily and robustly produced by the “liquid overlay” or “hanging drop” technique in specific microplates that can be used for plate reader [284,285] or microscopic measurements [179,286]. Alternatively, the use of non-taste cell lines expressing endogenous taste receptors and downstream signaling molecule can be of option. Since TRs have been found in multiple other tissues as the lungs, gastrointestinal tract and epithelium [287], cell lines as 16-HBE, HGT-1 or HuTu-80, which express natively components of taste signaling, have been used in patens from diverse companies (for overview see [19]). A limitation of this approach is that these cell lines often co-express sweet and bitter receptors, at difference with taste receptor cells.

6. Reporter Genes to Mark Specific Taste Cell Populations in Mice

Reporter genes are readily detectable gene products like β-Gal, luciferase or fluorescent proteins attached to a promoter sequence of another gene whose expression pattern is known or of interest. When used in transgenic organisms, the reporter gene product should thus allow to follow the activity pattern of the employed promoter [47,83,94,259,276,295]. Therefore, reporter genes can help to identify defined cell populations, if the used promoter sequence is specific for these cells and it allows to perform cell-type specific functional studies [296]. The first gustducin reporter mouse used the expression of the lacZ gene [111], but before these were introduced to study taste-specific questions, the only way to link a functional response to a defined cell type was to fix the investigated tissue/cell after live imaging and then proceed with phenotypic characterization, e.g., by immunostaining; the same cell had to be found and related to the imaging data. For example, Caicedo et al. aimed to study Ca2+ signaling in gustducin-positive cells. To do so, live imaging experiments were conducted, and afterwards the analyzed cells had to be re-identified by anti-gustducin immunostaining [159]. Thus, reporter gene approaches clearly facilitate the identification of the right cell population in live tissue. Currently, GFP is the most widely used reporter gene in the field of taste research (Table 4). The first GFP-based taste-related reporter mouse was presented by Huang and colleagues who exchanged the lacZ gene with a red-shifted GFP (BRL) from Wong’s cassette [79]. This achieved GFP expression in 95% of gustducin-GFP-positive cells [79]. Since the expression of the reporter gene product depends exclusively on the cell-type specific promoter, the recombinant promoter still drives the expression of the reporter protein in a specific cell upon knockout of the native gene product. Following such a strategy, it was possible to investigate taste signaling in defined cell types in absence or presence of key molecules in response to the different taste modalities (Table 4). Bitter responsiveness in the absence of gustducin was investigated by creating a reporter mouse in which GFP was expressed under the gustducin promoter, but with gustducin itself being knockedout [141]. Another reporter gene promoter to mark type II receptor cells was PLCβ2, which was used to create a knockin mouse expressing PLCβ2-GFP. Upon loading with CaOD, this allowed to demonstrate responsiveness GFP-positive cells to bitter compounds [297]. PLCβ2-GFP reporter mice were also used along with GAD-GFP mice. GAD is an isoform of the glutamic acid decarboxylase which is used as a marker for type III presynaptic cells [298]. Measuring Ca2+ responses in PLCβ2-GFP and GAD-GFP cells with CaOD significantly improved the understanding of the differences between type II and III cells in terms of expression of voltage-gated channels [49], signal transmission [114], neurotransmitter stimulation [33,42] and oxytocin-mediated modulation [142]. Further, IP3R3-GFP and TRMP5-GFP reporter mice were used to identify type II cells [50,113,299], and experiments with Fura-2 showed that only GFP-negative cells responded to depolarizing stimuli, thus confirming that type II cells do not possess voltage-gated Ca2+ channels [113]. To discriminate between sweet and umami taste cells (which are both of type II), mice expressing a T1R3-GFP fusion protein were generated (Table 4) [34,113,300,301,302,303,304,305]. As bitter is transduced by multiple receptors, the copy number of any individual bitter receptors might be rather low and therefore single T2R constructs may not be feasible. However, Oka and colleagues generated reporter mice expressing the blue-shifted GFP-derivate Sapphire under the control of the T2R32 promotor [46,306]. Sapphire has improved folding properties, is more pH stable and has excitation/emission peaks at 399/511 nm [307], thus allowing the combination with green-emitting Ca2+ indicators such as CaG. This showed, that type II cells expressing bitter receptors are also responsive to high KCl salt concentrations [46]. To address sourness and saltiness, PKD2L1-GFP [67] and ENaC-GFP reporter mice [48], respectively, were generated. In most reporter gene assays in the field of taste research, Ca2+ was measured with synthetic dyes (Table 4), either Fura-2 [277] or CaOD [33,49,114,297]. Alternatively, electrical recordings were used to assay Ca2+ transients [67,301,308,309]. Finally, one study presented mice where the GECI GCaMP3, expressed under the Pirt promoter, is present in type II and type III cells to investigate salt transduction [55,310].

7. Biosensor Cells to Determine Neurotransmitter Release from Taste Bud Cells

In general, biosensor cells (BCs) are living cells that detect the presence and concentration of a certain analytical substance. In taste research, they were used to study the response of taste cells to a stimulus, by reporting the release of neurotransmitters (Table 5) [315]. As some cell lines express a large variety of different native receptors, they can be directly used as sensor for certain ligands [316]. If the receptors of interest are not endogenously expressed, the cells can be genetically modified by heterologous expression [317]. In addition to the receptor, a biosensor cell-based system needs a transducer to report receptor activity to the experimenter. Often, BCs take advantage of intracellular signaling cascades activated by the receptor-ligand interaction, which amplifies the signal and facilitates its detection and measurement (Table 5) [316]. Accordingly, Ca2+ measurements with synthetic indicators are widely used (Table 5) because of their low cost and high efficiency and sensibility. BCs can be flexibly designed and are cheaper than antibodies or enzymes [318], but issues like inhomogeneous expression of receptors, depressed sensitivity and reproducibility need to be addressed [129]. As outlined below, BCs were useful tools to study the release of neurotransmitters and intercellular communication in taste buds (Table 5).
In a first attempt, BCs for serotonin (5HT) were made. These used CHO cells transiently expressing human high-affinity 5HT2C receptors, which trigger activation of PLCβ2, generation of IP3 and Ca2+ release from intracellular stores [319]. Thus, serotonin release could be assessed with these BCs by quantifying Ca2+ signals with Fura-2 live cell imaging (Figure 3) [320]. A second generation of serotonin BCs consisting of CHO cells stably expressing 5HT2C receptors were used to prove that 5HT is released by taste bud cells upon stimulation with bitter, sweet, or sour compounds [36]. To asses this, a Fura-2 loaded BC was positioned close to a freshly isolated mouse taste bud. Stimulation with KCl, sweet, sour or bitter compounds activated the BCs, indicating release of 5HT from taste bud cells (Figure 3). Since CHO cells natively express some purinergic receptors, the antagonist mianserin or the desensitization with a preincubation in high concentrations of ATP were used to differentiate serotoninergic from purinergic responses [36,105]. Notably, these BCs sensed 5HT concentrations in the nanomolar range, and thus allowed to detect the release of 5HT even from single dissociated taste cells [36,37]. Of course, the procedure was rather delicate and needed great care to position the BCs in immediate vicinity of the target cells to not lose the response. Furthermore, since only about one third of the trials were successful [36], stimulating preselection procedures of the best BCs prior to use with taste cells were applied [41].
In a similar fashion, BCs to sense ATP [37], noradrenaline (NA) [39] and GABA [40,41,104] were generated by transducing CHO cells with the purinergic receptors P2X2 and P2X3 [37,321], α1-adrenergic receptor (α1A) [39,322] and heteromeric GABAB receptors plus Gαqo5 (Table 5) [40]. Conversely, ATP-sensitive BCs based on COS-1 cells utilized their endogenous expression of P2Y receptors coupled to Ca2+ mobilization [32,323]. In this approach, a glass pipette was used to position the taste cell. This is advantageous, since the same pipette can be used for patch-clamp recordings to characterize the cell type and to trigger neurotransmitter release also by electrophysiology [32,323]. In the further course, dual BCs were generated (Table 5) by co-expressing two different receptors such as 5HT2c with α1A [39] or with P2X2/P2X3 [41,56,324]. Upon desensitization of one pathway, these dual BCs could be used to test alternatively one of the two neurotransmitters [40,41]. In some experiments, Ca2+ changes were simultaneously measured with Fura-2 in the taste cell and in the BC and the observed delay between the two transients was interpreted as a confirmation for communication via neurotransmitter [105].
BC-based research critically contributed to the understanding of the complex cell–cell communication in the taste bud. They unraveled the secretion of ATP by type II cells via an unconventional mechanism mediated by hemichannels [37], the release of 5HT, noradrenaline and GABA by type III cells upon voltage-gated Ca2+ entry [36,39,40,41] and of GABA by type I cells upon substance P stimulation [104]. Furthermore, the origin and the modulatory effects of glutamate [143], calcitonin gene-related peptide [324], adenosine [325], GABA [104] and acetylcholine [42] on taste cell-mediated neurotransmitter release were investigated. To develop BC-based systems for higher throughput, it could be advantageous to create co-cultures of biosensor cells and taste cells. In this case, rather than using a chemical indicator, it would be preferable to express genetically encoded sensors for Ca2+ or other second messengers such as cAMP [326,327] in the BCs and taste cells. This would be very useful in case of the generation of 3D cultures where loading with synthetic dyes may not be as efficient and homogenous as in 2D.

8. Conclusions and Future Perspectives

In taste research, two main streams run in parallel and are interconnected: one is the study of the mechanism underlying gustation, the other deals with the generation of artificial taste systems that can sense and discriminate between different tastants. Our concluding discussion will first focus on new potential approaches to discover the still missing pieces of the complex puzzle of taste physiology and to further refine the previous findings adding more details on the intracellular signaling and cell–cell communication. In a second part, ideas for novel sensing systems will be proposed that might mimic more closely the in vivo situation, but would be also compliant in terms of cost, technology and ethics.

8.1. New Approaches to Study Taste Physiology

The last 20 years have seen massive improvement in understanding taste physiology, both in the periphery and in the CNS as well as at the molecular, cellular and network levels. However, most studies focused on the ubiquitous intracellular signal Ca2+, potentially leading to an underestimation of other important factors. Indeed, the taste transduction pathways might be much more complex than the models proposed in most reviews including the pathway shown in Figure 1. For example, many knockout mouse models suggest that there may be additional signaling pathways involved, since taste sensation, nerve response and preferences for test compounds are often not completely abolished by eliminating a critical component of the canonical pathway including taste receptors, gustducin or TRPM5 channels [76,86,300,330]. Looking only at Ca2+ may not suffice to discriminate between these different pathways, as they may all induce a similar Ca2+ increase but with different underlying mechanisms. Along these lines, G-proteins other than gustducin are likely also involved in the signaling cascade [275,331] as well as other second messengers than Ca2+, such as cAMP [141,165]. Moreover, sweet signal transduction mechanisms may exist that bypass the activation of sweet taste receptors and instead use glucose transporters (GLUT) [86,87,332]. The pathway usage might be different even for compounds falling into the same taste modality [139], as it might be true for nutritive sugars and synthetic sweeteners or bitter compounds utilizing a PLCβ2-independent pathway at higher concentrations [333]. In this context, it would be helpful to use genetically encoded molecular biosensors for different signaling components such as cAMP and glucose [252,334] or a plethora of other factors (for a comprehensive database, see https://biosensordb.ucsd.edu). Via standard genetic engineering tools, such biosensors can be expressed in recombinant tongue-derived cell lines [179], introduced into primary taste cells via viral infection or electroporation or in transgenic mice for in situ or in vivo studies.
Next, it is widely recognized that specificity of second messenger-based cellular signal transduction involves local organization, by restricting signals to specific organelles and even to microdomains [335]. Until now, this aspect of signal compartmentation has been completely neglected in the investigation of taste transduction, although it is well known that taste cells use many different sources of Ca2+ [49,113]. Accordingly, although some taste responses are mediated by Ca2+ influx into receptor cells [50,117], the underlying molecular mechanism is unknown, since these cells do not express voltage-gated calcium channels. Finally, measurements of cytoplasmatic Ca2+ in combination with drugs that empty the endoplasmic reticulum or block the activity of mitochondria showed an important role of these organelles in the Ca2+ homeostasis within the taste bud [168,169]. As valuable as these insights were, future approaches should measure Ca2+ signals in the corresponding compartments by appropriate subcellular targeting of genetically encoded probes [336]. In synthesis, switching from chemical dyes to genetically encoded biosensors and adding other signaling components to Ca2+ will help to further improve our understanding of the taste signaling cascades.

8.2. Development of New In Vitro Taste Systems

Taste cell-based biosensors have a great potential for either basic research or for industrial applications, such as food safety and discovery of new ligands. On the one side, biosensor systems highly specialized for one taste modality are good testing platforms for discovering new agonists and antagonists to specific receptors/ions. Embedded into analytic devices they might serve to detect for example toxins [129] or to screen compound libraries [271,279]. On the other side, taste cell-based biosensors able to respond to flavors of different modalities could interpret complex flavor patterns and may be useful for quality control of food, drugs and the development of new palatable mixtures, such as in search for new sweet beverages with low caloric content.
On the long run, a complex taste cell-based artificial tongue system can be envisaged, which should fulfil the following criteria. It should 1) reproduce the complexity of the taste bud with respect to structure and functionality, 2) be representative for human gustation and 3) be implementable for high throughput. Considering the complexity of taste buds, 3D taste cell cultures with heterogeneous cell populations might come closest to such an idea. For reasons of reproducibility, these 3D culture could be formed as spheroids [179], cell chip cultures (Figure 4), and organoids derived from progenitor cells [127] or microfluidic devices [337]. Spheroids, prepared with tongue-derived human cells (HTC-8) by liquid overlay technique on commercially available low-attachment plates, were successfully used to measure real-time responses upon application of bitter compounds [179]. Comparable results were obtained upon 3D cultivation of HTC-8-G-GECO cells in special Dynarray cell chips, which can be used for live imaging experiments in perfusion conditions, as they are made of transparent materials and have porous walls (Figure 4, original data from us). Furthermore, the chips can be used in bioreactors with circulating media and with the option of different apical and basal perfusions to favor cell polarization. Further, organoids were generated from Lgr5-positive mouse progenitor cells, which could be expanded and differentiated into the different taste cell types [126,127]. However, neither the purification of such multipotent cells from human tongue, nor the generation of mature taste cells by differentiating human induced pluripotent stem cells have been explored so far. Recent progress in the mechanisms of taste cell development [124,127,128] suggest further steps in that direction. Another effort to recreate a multicellular taste cell-based system with a potential integration in a microfluid device for industrial application, has been recently made with the help of tongue extracellular matrix [337], which was generated from porcine tongue and used to prepare primary 2D and 3D taste cell cultures and co-cultures with neurons [337]. This improved both the expression of gustatory markers and the functionality of taste cells, furthermore taste cell signals were transmitted to the neurons. These findings were applied to test wine [10].
Finally, on the road to an artificial tongue system, the development of optimal cell culture conditions needs to be flanked by novel sensor technologies for more specific and comprehensive readouts. For example, optical and electrical sensors could be used in parallel. Patterns of Ca2+ changes in combination with voltage current recordings may allow to discriminate not only between the different taste modalities but also between compounds of the same families, such as natural versus artificial sweeteners. Novel, sophisticated imaging systems suitable to acquire multiple fluorescence signals from microplates with cellular resolution are now available and high-content imaging systems allow the acquisition of confocal images in thick tissue/probes up to a 1536 wells format with multiple lasers and dichroic filters [338,339]. In addition, optical tissue clearing protocols start also to be applied to 3D cultures, which could largely improve expression analysis in three dimensions [340]. For enhanced throughput of electrical recordings, new devices such as multielectrode arrays or automatic patch-clamp platforms allow to clamp hundreds of cells simultaneously [341].
In summary, the use of taste cells to develop biosensor systems for gustation is a new field with a wide range of possible applications [5,6,7,9,205]. Next-generation biosensor systems could now be developed with 3D taste cell cultures that can be used for both high-content imaging and live imaging microscopy. The use of genetically encoded biosensors to measure different signaling molecules in defined cellular compartments will allow higher flexibility, easier handling and more specific readouts. A major challenge will be to couple 3D cell cultures expressing such sensors to microdevices able to read optical and electrical signals, in order to develop portable and user friendly “pocket tongues”.

9. Literature Research

Literature research used the electronic databases Google Scholar and PubMed, which were screened by two independent researchers for peer-reviewed publications written in English. The selection of articles was carried out by evaluating first heading and abstract, then reading the whole text. Search terms used were “taste”, “gustation”, ”calcium”, ”pH”, ”voltage”, ”dye”, “genetically encoded sensor” and “biosensor”: such terms were differently combined with the Boolean “AND” operation. Most hits were found with “taste AND calcium”. We included all articles without time restriction, while patents were excluded. Further, only studies concerning gustation in the taste bud and in the CNS were included. Conversely, studies in extraoral tissues and in specific brain regions in respect to food reward, expectation and decision making were omitted. Only articles applying optical biosensors in the context of an optical functional readout, such as plate reader or microscope, were included in the table. Other functional read out such as electrophysiology, or studies using only immunohistochemistry or biochemistry were mainly not discussed.

Author Contributions

Conceptualization, E.v.M. and T.C.; investigation, E.v.M. and T.C.; writing—original draft preparation, E.v.M. and T.C.; writing—review and editing, K.R., M.H. and R.R.; visualization, E.v.M. and T.C.; supervision, K.R., M.H. and R.R.; project administration, R.R.; funding acquisition, M.H. and R.R. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded by the German Federal Ministry of Education and Research (BMBF) as part of the Innovation Partnership M2Aind, project M2OGA (03FH8I02IA) within the framework Starke Fachhochschulen–Impuls für die Region (FH-Impuls).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ali, J.; Najeeb, J.; Asim Ali, M.; Farhan Aslam, M.; Raza, A. Biosensors: Their Fundamentals, Designs, Types and Most Recent Impactful Applications: A Review. J. Biosens. Bioelectron. 2017, 8. [Google Scholar] [CrossRef]
  2. Liu, Q.; Wu, C.; Cai, H.; Hu, N.; Zhou, J.; Wang, P. Cell-based biosensors and their application in biomedicine. Chem. Rev. 2014, 114, 6423–6461. [Google Scholar] [CrossRef]
  3. Podrażka, M.; Bączyńska, E.; Kundys, M.; Jeleń, P.S.; Witkowska Nery, E. Electronic Tongue-A Tool for All Tastes? Biosensors (Basel) 2017, 8, 3. [Google Scholar] [CrossRef] [Green Version]
  4. Ha, D.; Sun, Q.; Su, K.; Wan, H.; Li, H.; Xu, N.; Sun, F.; Zhuang, L.; Hu, N.; Wang, P. Recent achievements in electronic tongue and bioelectronic tongue as taste sensors. Sens. Actuators B Chem. 2015, 207, 1136–1146. [Google Scholar] [CrossRef]
  5. Wu, C.; Lillehoj, P.B.; Wang, P. Bioanalytical and chemical sensors using living taste, olfactory, and neural cells and tissues: A short review. Analyst 2015, 140, 7048–7061. [Google Scholar] [CrossRef] [PubMed]
  6. Wu, C.; Du, Y.-W.; Huang, L.; Ben-Shoshan Galeczki, Y.; Dagan-Wiener, A.; Naim, M.; Niv, M.Y.; Wang, P. Biomimetic Sensors for the Senses: Towards Better Understanding of Taste and Odor Sensation. Sensors (Basel) 2017, 17, 2881. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Wasilewski, T.; Kamysz, W.; Gębicki, J. Bioelectronic tongue: Current status and perspectives. Biosens. Bioelectron. 2020, 150, 111923. [Google Scholar] [CrossRef]
  8. Bioinspired Smell and Taste Sensors, 1st ed.; Wang, P.; Liu, Q.; Wu, C.; Hsia, K.J. (Eds.) Springer: Dordrecht, The Netherlands; Beijing, China, 2015; ISBN 9789401773324. [Google Scholar]
  9. Woertz, K.; Tissen, C.; Kleinebudde, P.; Breitkreutz, J. Taste sensing systems (electronic tongues) for pharmaceutical applications. Int. J. Pharm. 2011, 417, 256–271. [Google Scholar] [CrossRef]
  10. Gutiérrez, M.; Llobera, A.; Vila-Planas, J.; Capdevila, F.; Demming, S.; Büttgenbach, S.; Mínguez, S.; Jiménez-Jorquera, C. Hybrid electronic tongue based on optical and electrochemical microsensors for quality control of wine. Analyst 2010, 135, 1718–1725. [Google Scholar] [CrossRef]
  11. Laffitte, A.; Neiers, F.; Briand, L. Functional roles of the sweet taste receptor in oral and extraoral tissues. Curr. Opin. Clin. Nutr. Metab. Care 2014, 17, 379–385. [Google Scholar] [CrossRef]
  12. Lu, P.; Zhang, C.-H.; Lifshitz, L.M.; ZhuGe, R. Extraoral bitter taste receptors in health and disease. J. Gen. Physiol. 2017, 149, 181–197. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Yamamoto, K.; Ishimaru, Y. Oral and extra-oral taste perception. Semin. Cell Dev. Biol. 2013, 24, 240–246. [Google Scholar] [CrossRef]
  14. Beauchamp, G.K. Why do we like sweet taste: A bitter tale? Physiol. Behav. 2016, 164, 432–437. [Google Scholar] [CrossRef] [Green Version]
  15. Chaudhari, N.; Roper, S.D. The cell biology of taste. J. Cell Biol. 2010, 190, 285–296. [Google Scholar] [CrossRef] [Green Version]
  16. Mennella, J.A.; Spector, A.C.; Reed, D.R.; Coldwell, S.E. The Bad Taste of Medicines: Overview of Basic Research on Bitter Taste. Clin. Ther. 2013, 35, 1225–1246. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Ley, J.P. Masking Bitter Taste by Molecules. Chemosens. Percept. 2008, 1, 58–77. [Google Scholar] [CrossRef]
  18. Clark, J.E. Taste and flavour: Their importance in food choice and acceptance. Proc. Nutr. Soc. 1998, 57, 639–643. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Riedel, K.; Sombroek, D.; Fiedler, B.; Siems, K.; Krohn, M. Human cell-based taste perception—A bittersweet job for industry. Nat. Prod. Rep. 2017, 34, 484–495. [Google Scholar] [CrossRef]
  20. Roper, S.D.; Chaudhari, N. Taste buds: Cells, signals and synapses. Nat. Rev. Neurosci. 2017, 18, 485–497. [Google Scholar] [CrossRef]
  21. Lindemann, B. Receptor seeks ligand: On the way to cloning the molecular receptors for sweet and bitter taste. Nat. Med. 1999, 5, 381–382. [Google Scholar] [CrossRef]
  22. Montmayeur, J.-P.; Matsunami, H. Receptors for bitter and sweet taste. Curr. Opin. Neurobiol. 2002, 12, 366–371. [Google Scholar] [CrossRef]
  23. Witt, M.; Reutter, K.; Miller, I.J., Jr. Morphology of the Peripheral Taste System. In Handbook of Olfaction and Gustation; CRC Press: Boca Raton, FL, USA, 2003; pp. 1142–1188. [Google Scholar]
  24. Kikut-Ligaj, D.; Trzcielińska-Lorych, J. How taste works: Cells, receptors and gustatory perception. Cell. Mol. Biol. Lett. 2015, 20, 699–716. [Google Scholar] [CrossRef] [PubMed]
  25. Scott, K. Taste Recognition: Food for Thought. Neuron 2005, 48, 455–464. [Google Scholar] [CrossRef] [Green Version]
  26. Roper, S.D. Taste buds as peripheral chemosensory processors. Semin. Cell Dev. Biol. 2013, 24, 71–79. [Google Scholar] [CrossRef] [Green Version]
  27. Bannwarth, M.; Correa, I.R.; Sztretye, M.; Pouvreau, S.; Fellay, C.; Aebischer, A.; Royer, L.; Rois, E.; Johnsson, K. Indo-1 derivatives for local calcium sensing. ACS Chem. Biol. 2009, 4, 179–190. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Vandenbeuch, A.; Anderson, C.B.; Parnes, J.; Enjyoji, K.; Robson, S.C.; Finger, T.E.; Kinnamon, S.C. Role of the ectonucleotidase NTPDase2 in taste bud function. Proc. Natl. Acad. Sci. USA 2013, 110, 14789–14794. [Google Scholar] [CrossRef] [Green Version]
  29. Yee, C.L.; Yang, R.; Böttger, B.; Finger, T.E.; Kinnamon, J.C. “Type III” cells of rat taste buds: Immunohistochemical and ultrastructural studies of neuron-specific enolase, protein gene product 9.5, and serotonin. J. Comp. Neurol. 2001, 440, 97–108. [Google Scholar] [CrossRef]
  30. Miura, H.; Kusakabe, Y.; Harada, S. Cell lineage and differentiation in taste buds. Arch. Histol. Cytol. 2006, 69, 209–225. [Google Scholar] [CrossRef]
  31. Finger, T.E.; Danilova, V.; Barrows, J.; Bartel, D.L.; Vigers, A.J.; Stone, L.; Hellekant, G.; Kinnamon, S.C. ATP signaling is crucial for communication from taste buds to gustatory nerves. Science 2005, 310, 1495–1499. [Google Scholar] [CrossRef]
  32. Romanov, R.A.; Rogachevskaja, O.A.; Bystrova, M.F.; Jiang, P.; Margolskee, R.F.; Kolesnikov, S.S. Afferent neurotransmission mediated by hemichannels in mammalian taste cells. EMBO J. 2007, 26, 657–667. [Google Scholar] [CrossRef]
  33. Dando, R.; Roper, S.D. Cell-to-cell communication in intact taste buds through ATP signalling from pannexin 1 gap junction hemichannels. J. Physiol. (Lond) 2009, 587, 5899–5906. [Google Scholar] [CrossRef]
  34. Taruno, A.; Vingtdeux, V.; Ohmoto, M.; Ma, Z.; Dvoryanchikov, G.; Li, A.; Adrien, L.; Zhao, H.; Leung, S.; Abernethy, M.; et al. CALHM1 ion channel mediates purinergic neurotransmission of sweet, bitter and umami tastes. Nature 2013, 495, 223–226. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Romanov, R.A.; Lasher, R.S.; High, B.; Savidge, L.E.; Lawson, A.; Rogachevskaja, O.A.; Zhao, H.; Rogachevsky, V.V.; Bystrova, M.F.; Churbanov, G.D.; et al. Chemical synapses without synaptic vesicles: Purinergic neurotransmission via a CALHM1 channel-mitochondrial signaling complex. Sci. Signal. 2018, 11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Huang, Y.-J.; Maruyama, Y.; Lu, K.-S.; Pereira, E.; Plonsky, I.; Baur, J.E.; Wu, D.; Roper, S.D. Mouse taste buds use serotonin as a neurotransmitter. J. Neurosci. 2005, 25, 843–847. [Google Scholar] [CrossRef] [PubMed]
  37. Huang, Y.-J.; Maruyama, Y.; Dvoryanchikov, G.; Pereira, E.; Chaudhari, N.; Roper, S.D. The role of pannexin 1 hemichannels in ATP release and cell-cell communication in mouse taste buds. Proc. Natl. Acad. Sci. USA 2007, 104, 6436–6441. [Google Scholar] [CrossRef] [Green Version]
  38. Larson, E.D.; Vandenbeuch, A.; Voigt, A.; Meyerhof, W.; Kinnamon, S.C.; Finger, T.E. The Role of 5-HT3 Receptors in Signaling from Taste Buds to Nerves. J. Neurosci. 2015, 35, 15984–15995. [Google Scholar] [CrossRef]
  39. Huang, Y.A.; Maruyama, Y.; Roper, S.D. Norepinephrine is coreleased with serotonin in mouse taste buds. J. Neurosci. 2008, 28, 13088–13093. [Google Scholar] [CrossRef] [Green Version]
  40. Huang, Y.A.; Pereira, E.; Roper, S.D. Acid stimulation (sour taste) elicits GABA and serotonin release from mouse taste cells. PLoS ONE 2011, 6, e25471. [Google Scholar] [CrossRef] [Green Version]
  41. Dvoryanchikov, G.; Huang, Y.A.; Barro-Soria, R.; Chaudhari, N.; Roper, S.D. GABA, its receptors, and GABAergic inhibition in mouse taste buds. J. Neurosci. 2011, 31, 5782–5791. [Google Scholar] [CrossRef]
  42. Dando, R.; Roper, S.D. Acetylcholine is released from taste cells, enhancing taste signalling. J. Physiol. (Lond) 2012, 590, 3009–3017. [Google Scholar] [CrossRef] [Green Version]
  43. Gilbertson, T.A.; Damak, S.; Margolskee, R.F. The molecular physiology of taste transduction. Curr. Opin. Neurobiol. 2000, 10, 519–527. [Google Scholar] [CrossRef]
  44. Roper, S.D. Parallel processing in mammalian taste buds? Physiol. Behav. 2009, 97, 604–608. [Google Scholar] [CrossRef] [Green Version]
  45. Roper, S.D. Signal transduction and information processing in mammalian taste buds. Pflugers Arch. 2007, 454, 759–776. [Google Scholar] [CrossRef] [PubMed]
  46. Oka, Y.; Butnaru, M.; Buchholtz, L.v.; Ryba, N.J.P.; Zuker, C.S. High salt recruits aversive taste pathways. Nature 2013, 494, 472–475. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Chandrashekar, J.; Mueller, K.L.; Hoon, M.A.; Adler, E.; Feng, L.; Guo, W.; Zuker, C.S.; Ryba, N.J.P. T2Rs Function as Bitter Taste Receptors. Cell 2000, 100, 703–711. [Google Scholar] [CrossRef] [Green Version]
  48. Chandrashekar, J.; Kuhn, C.; Oka, Y.; Yarmolinsky, D.A.; Hummler, E.; Ryba, N.J.P.; Zuker, C.S. The cells and peripheral representation of sodium taste in mice. Nature 2010, 464, 297–301. [Google Scholar] [CrossRef] [Green Version]
  49. DeFazio, R.A.; Dvoryanchikov, G.; Maruyama, Y.; Kim, J.W.; Pereira, E.; Roper, S.D.; Chaudhari, N. Separate populations of receptor cells and presynaptic cells in mouse taste buds. J. Neurosci. 2006, 26, 3971–3980. [Google Scholar] [CrossRef] [Green Version]
  50. Hacker, K.; Laskowski, A.; Feng, L.; Restrepo, D.; Medler, K. Evidence for two populations of bitter responsive taste cells in mice. J. Neurophysiol. 2008, 99, 1503–1514. [Google Scholar] [CrossRef] [Green Version]
  51. Ossebaard, C.A.; Smith, D.V. Effect of amiloride on the taste of NaCl, Na-gluconate and KCl in humans: Implications for Na+ receptor mechanisms. Chem. Senses 1995, 20, 37–46. [Google Scholar] [CrossRef]
  52. Feldman, G.M.; Mogyorosi, A.; Heck, G.L.; Desimone, J.A.; Santos, C.R.; Clary, R.A.; Lyall, V. Salt-evoked lingual surface potential in humans. J. Neurophysiol. 2003, 90, 2060–2064. [Google Scholar] [CrossRef]
  53. Lyall, V.; Heck, G.L.; Vinnikova, A.K.; Ghosh, S.; Phan, T.-H.T.; Alam, R.I.; Russell, O.F.; Malik, S.A.; Bigbee, J.W.; Desimone, J.A. The mammalian amiloride-insensitive non-specific salt taste receptor is a vanilloid receptor-1 variant. J. Physiol. (Lond) 2004, 558, 147–159. [Google Scholar] [CrossRef]
  54. Lyall, V.; Heck, G.L.; Vinnikova, A.K.; Ghosh, S.; Phan, T.-H.T.; Desimone, J.A. A novel vanilloid receptor-1 (VR-1) variant mammalian salt taste receptor. Chem. Senses 2005, 30 (Suppl. 1), i42–i43. [Google Scholar] [CrossRef] [Green Version]
  55. Roebber, J.K.; Roper, S.D.; Chaudhari, N. The Role of the Anion in Salt (NaCl) Detection by Mouse Taste Buds. J. Neurosci. 2019, 39, 6224–6232. [Google Scholar] [CrossRef] [Green Version]
  56. Huang, Y.A.; Maruyama, Y.; Stimac, R.; Roper, S.D. Presynaptic (Type III) cells in mouse taste buds sense sour (acid) taste. J. Physiol. (Lond) 2008, 586, 2903–2912. [Google Scholar] [CrossRef] [PubMed]
  57. Kataoka, S.; Yang, R.; Ishimaru, Y.; Matsunami, H.; Sévigny, J.; Kinnamon, J.C.; Finger, T.E. The candidate sour taste receptor, PKD2L1, is expressed by type III taste cells in the mouse. Chem. Senses 2008, 33, 243–254. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Ramos Da Conceicao Neta, E.R.; Johanningsmeier, S.D.; McFeeters, R.F. The Chemistry and Physiology of Sour Taste—A Review. J. Food Sci. 2007, 72, R33–R38. [Google Scholar] [CrossRef] [PubMed]
  59. Richter, T.A.; Caicedo, A.; Roper, S.D. Sour taste stimuli evoke Ca2+ and pH responses in mouse taste cells. J. Physiol. (Lond) 2003, 547, 475–483. [Google Scholar] [CrossRef] [PubMed]
  60. Miyamoto, T.; Okada, Y.; Sato, T. Ionic basis of receptor potential of frog taste cells induced by acid stimuli. J. Physiol. (Lond) 1988, 405, 699–711. [Google Scholar] [CrossRef] [Green Version]
  61. Kinnamon, S.C.; Roper, S.D. Membrane properties of isolated mudpuppy taste cells. J. Gen. Physiol. 1988, 91, 351–371. [Google Scholar] [CrossRef] [Green Version]
  62. Gilbertson, T.A.; Roper, S.D.; Kinnamon, S.C. Proton currents through amiloride-sensitive Na+ channels in isolated hamster taste cells: Enhancement by vasopressin and cAMP. Neuron 1993, 10, 931–942. [Google Scholar] [CrossRef]
  63. Miyamoto, T.; Fujiyama, R.; Okada, Y.; Sato, T. Sour transduction involves activation of NPPB-sensitive conductance in mouse taste cells. J. Neurophysiol. 1998, 80, 1852–1859. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Ugawa, S.; Minami, Y.; Guo, W.; Saishin, Y.; Takatsuji, K.; Yamamoto, T.; Tohyama, M.; Shimada, S. Receptor that leaves a sour taste in the mouth. Nature 1998, 395, 555–556. [Google Scholar] [CrossRef] [PubMed]
  65. Stevens, D.R.; Seifert, R.; Bufe, B.; Müller, F.; Kremmer, E.; Gauss, R.; Meyerhof, W.; Kaupp, U.B.; Lindemann, B. Hyperpolarization-activated channels HCN1 and HCN4 mediate responses to sour stimuli. Nature 2001, 413, 631–635. [Google Scholar] [CrossRef] [PubMed]
  66. Huang, A.L.; Chen, X.; Hoon, M.A.; Chandrashekar, J.; Guo, W.; Tränkner, D.; Ryba, N.J.P.; Zuker, C.S. The cells and logic for mammalian sour taste detection. Nature 2006, 442, 934–938. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Lyall, V.; Alam, R.I.; Phan, D.Q.; Ereso, G.L.; Phan, T.H.; Malik, S.A.; Montrose, M.H.; Chu, S.; Heck, G.L.; Feldman, G.M.; et al. Decrease in rat taste receptor cell intracellular pH is the proximate stimulus in sour taste transduction. Am. J. Physiol. Cell Physiol. 2001, 281, C1005–C1013. [Google Scholar] [CrossRef] [Green Version]
  68. Nelson, T.M.; Lopezjimenez, N.D.; Tessarollo, L.; Inoue, M.; Bachmanov, A.A.; Sullivan, S.L. Taste function in mice with a targeted mutation of the pkd1l3 gene. Chem. Senses 2010, 35, 565–577. [Google Scholar] [CrossRef]
  69. Teng, B.; Wilson, C.E.; Tu, Y.-H.; Joshi, N.R.; Kinnamon, S.C.; Liman, E.R. Cellular and Neural Responses to Sour Stimuli Require the Proton Channel Otop1. Curr. Biol. 2019, 29, 3647–3656.e5. [Google Scholar] [CrossRef] [Green Version]
  70. Go, Y.; Satta, Y.; Takenaka, O.; Takahata, N. Lineage-specific loss of function of bitter taste receptor genes in humans and nonhuman primates. Genetics 2005, 170, 313–326. [Google Scholar] [CrossRef] [Green Version]
  71. Adler, E.; Hoon, M.A.; Mueller, K.L.; Chandrashekar, J.; Ryba, N.J.P.; Zuker, C.S. A Novel Family of Mammalian Taste Receptors. Cell 2000, 100, 693–702. [Google Scholar] [CrossRef] [Green Version]
  72. Kuhn, C.; Bufe, B.; Winnig, M.; Hofmann, T.; Frank, O.; Behrens, M.; Lewtschenko, T.; Slack, J.P.; Ward, C.D.; Meyerhof, W. Bitter taste receptors for saccharin and acesulfame K. J. Neurosci. 2004, 24, 10260–10265. [Google Scholar] [CrossRef] [Green Version]
  73. Meyerhof, W.; Batram, C.; Kuhn, C.; Brockhoff, A.; Chudoba, E.; Bufe, B.; Appendino, G.; Behrens, M. The molecular receptive ranges of human TAS2R bitter taste receptors. Chem. Senses 2010, 35, 157–170. [Google Scholar] [CrossRef] [PubMed]
  74. Caicedo, A.; Roper, S.D. Taste receptor cells that discriminate between bitter stimuli. Science 2001, 291, 1557–1560. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Matsunami, H.; Montmayeur, J.P.; Buck, L.B. A family of candidate taste receptors in human and mouse. Nature 2000, 404, 601–604. [Google Scholar] [CrossRef] [PubMed]
  76. Wong, G.T.; Gannon, K.S.; Margolskee, R.F. Transduction of bitter and sweet taste by gustducin. Nature 1996, 381, 796–800. [Google Scholar] [CrossRef]
  77. Choi, M.; Lee, W.M.; Yun, S.H. Intravital Microscopic Interrogation of Peripheral Taste Sensation. Sci. Rep. 2015, 5, 8661. [Google Scholar] [CrossRef]
  78. Ming, D.; Ninomiya, Y.; Margolskee, R.F. Blocking taste receptor activation of gustducin inhibits gustatory responses to bitter compounds. Proc. Natl. Acad. Sci. USA 1999, 96, 9903–9908. [Google Scholar] [CrossRef] [Green Version]
  79. Huang, L.; Shanker, Y.G.; Dubauskaite, J.; Zheng, J.Z.; Yan, W.; Rosenzweig, S.; Spielman, A.I.; Max, M.; Margolskee, R.F. Gγ13 colocalizes with gustducin in taste receptor cells and mediates IP 3 responses to bitter denatonium. Nat. Neurosci. 1999, 2, 1055–1062. [Google Scholar] [CrossRef]
  80. Liu, D.; Liman, E.R. Intracellular Ca2+ and the phospholipid PIP2 regulate the taste transduction ion channel TRPM5. Proc. Natl. Acad. Sci. USA 2003, 100, 15160–15165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  81. Chandrashekar, J.; Hoon, M.A.; Ryba, N.J.P.; Zuker, C.S. The receptors and cells for mammalian taste. Nature 2006, 444, 288–294. [Google Scholar] [CrossRef] [PubMed]
  82. Avau, B.; Depoortere, I. The bitter truth about bitter taste receptors: Beyond sensing bitter in the oral cavity. Acta Physiol. (Oxf) 2016, 216, 407–420. [Google Scholar] [CrossRef] [PubMed]
  83. Nelson, G.; Hoon, M.A.; Chandrashekar, J.; Zhang, Y.; Ryba, N.J.P.; Zuker, C.S. Mammalian Sweet Taste Receptors. Cell 2001, 106, 381–390. [Google Scholar] [CrossRef] [Green Version]
  84. Kitagawa, M.; Kusakabe, Y.; Miura, H.; Ninomiya, Y.; Hino, A. Molecular Genetic Identification of a Candidate Receptor Gene for Sweet Taste. Biochem. Biophys. Res. Commun. 2001, 283, 236–242. [Google Scholar] [CrossRef] [PubMed]
  85. Max, M.; Shanker, Y.G.; Huang, L.; Rong, M.; Liu, Z.; Campagne, F.; Weinstein, H.; Damak, S.; Margolskee, R.F. Tas1r3, encoding a new candidate taste receptor, is allelic to the sweet responsiveness locus Sac. Nat. Genet. 2001, 28, 58–63. [Google Scholar] [CrossRef] [PubMed]
  86. Damak, S.; Rong, M.; Yasumatsu, K.; Kokrashvili, Z.; Varadarajan, V.; Zou, S.; Jiang, P.; Ninomiya, Y.; Margolskee, R.F. Detection of sweet and umami taste in the absence of taste receptor T1r3. Science 2003, 301, 850–853. [Google Scholar] [CrossRef] [PubMed]
  87. Yee, K.K.; Sukumaran, S.K.; Kotha, R.; Gilbertson, T.A.; Margolskee, R.F. Glucose transporters and ATP-gated K+ (KATP) metabolic sensors are present in type 1 taste receptor 3 (T1r3)-expressing taste cells. Proc. Natl. Acad. Sci. USA 2011, 108, 5431–5436. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Avenet, P.; Lindemann, B. Patch-clamp study of isolated taste receptor cells of the frog. J. Membr. Biol. 1987, 97, 223–240. [Google Scholar] [CrossRef] [PubMed]
  89. Kurihara, K.; Koyama, N. High activity of adenyl cyclase in olfactory and gustatory organs. Biochem. Biophys. Res. Commun. 1972, 48, 30–34. [Google Scholar] [CrossRef]
  90. Naim, M.; Ronen, T.; Striem, B.J.; Levinson, M.; Zehavi, U. Adenylate cyclase responses to sucrose stimulation in membranes of pig circumvallate taste papillae. Comp. Biochem. Physiol. Part B Comp. Biochem. 1991, 100, 455–458. [Google Scholar] [CrossRef]
  91. Striem, B.J.; Pace, U.; Zehavi, U.; Naim, M.; Lancet, D. Sweet tastants stimulate adenylate cyclase coupled to GTP-binding protein in rat tongue membranes. Biochem. J. 1989, 260, 121–126. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Striem, B.J.; Naim, M.; Lindemann, B. Generation of Cyclic AMP in Taste Buds of the Rat Circumvallate Papilla in Response to Sucrose. Cell Physiol. Biochem. 1991, 1, 46–54. [Google Scholar] [CrossRef] [Green Version]
  93. Li, X.; Staszewski, L.; Xu, H.; Durick, K.; Zoller, M.; Adler, E. Human receptors for sweet and umami taste. Proc. Natl. Acad. Sci. USA 2002, 99, 4692–4696. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  94. Nelson, G.; Chandrashekar, J.; Hoon, M.A.; Feng, L.; Zhao, G.; Ryba, N.J.P.; Zuker, C.S. An amino-acid taste receptor. Nature 2002, 416, 199–202. [Google Scholar] [CrossRef] [PubMed]
  95. Kinnamon, S.C. Umami taste transduction mechanisms. Am. J. Clin. Nutr. 2009, 90, 753S–755S. [Google Scholar] [CrossRef] [PubMed]
  96. Chandrashekar, J.; Yarmolinsky, D.; Buchholtz, L.v.; Oka, Y.; Sly, W.; Ryba, N.J.P.; Zuker, C.S. The taste of carbonation. Science 2009, 326, 443–445. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  97. Dramane, G.; Abdoul-Azize, S.; Hichami, A.; Vögtle, T.; Akpona, S.; Chouabe, C.; Sadou, H.; Nieswandt, B.; Besnard, P.; Khan, N.A. STIM1 regulates calcium signaling in taste bud cells and preference for fat in mice. J. Clin. Investig. 2012, 122, 2267–2282. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  98. Ozdener, M.H.; Subramaniam, S.; Sundaresan, S.; Sery, O.; Hashimoto, T.; Asakawa, Y.; Besnard, P.; Abumrad, N.A.; Khan, N.A. CD36- and GPR120-mediated Ca(2)(+) signaling in human taste bud cells mediates differential responses to fatty acids and is altered in obese mice. Gastroenterology 2014, 146, 995–1005. [Google Scholar] [CrossRef] [Green Version]
  99. Ohsu, T.; Amino, Y.; Nagasaki, H.; Yamanaka, T.; Takeshita, S.; Hatanaka, T.; Maruyama, Y.; Miyamura, N.; Eto, Y. Involvement of the calcium-sensing receptor in human taste perception. J. Biol. Chem. 2010, 285, 1016–1022. [Google Scholar] [CrossRef] [Green Version]
  100. Maruyama, Y.; Yasuda, R.; Kuroda, M.; Eto, Y. Kokumi Substances, Enhancers of Basic Tastes, Induce Responses in Calcium-Sensing Receptor Expressing Taste Cells. PLoS ONE 2012, 7, e34489. [Google Scholar] [CrossRef] [Green Version]
  101. Ishida, Y.; Ugawa, S.; Ueda, T.; Murakami, S.; Shimada, S. Vanilloid receptor subtype-1 (VR1) is specifically localized to taste papillae. Mol. Brain Res. 2002, 107, 17–22. [Google Scholar] [CrossRef]
  102. Smutzer, G.; Devassy, R.K. Integrating TRPV1 Receptor Function with Capsaicin Psychophysics. Adv. Pharmacol. Sci. 2016, 2016, 1512457. [Google Scholar] [CrossRef] [Green Version]
  103. Hacker, K.; Medler, K.F. Mitochondrial calcium buffering contributes to the maintenance of Basal calcium levels in mouse taste cells. J. Neurophysiol. 2008, 100, 2177–2191. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  104. Huang, Y.A.; Dando, R.; Roper, S.D. Autocrine and paracrine roles for ATP and serotonin in mouse taste buds. J. Neurosci. 2009, 29, 13909–13918. [Google Scholar] [CrossRef] [PubMed]
  105. Eguchi, K.; Ohtubo, Y.; Yoshii, K. Functional expression of M3, a muscarinic acetylcholine receptor subtype, in taste bud cells of mouse fungiform papillae. Chem. Senses 2008, 33, 47–55. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Simon, S.A.; Baggett, H.C. Identification of muscarinic acetylcholine receptors in isolated canine lingual epithelia via voltage clamp measurements. Arch. Oral Biol. 1992, 37, 685–690. [Google Scholar] [CrossRef]
  107. Ogura, T.; Lin, W. Acetylcholine and acetylcholine receptors in taste receptor cells. Chem. Senses 2005, 30 (Suppl. 1), i41. [Google Scholar] [CrossRef] [Green Version]
  108. Huang, A.Y.; Wu, S.Y. Substance P as a putative efferent transmitter mediates GABAergic inhibition in mouse taste buds. Br. J. Pharmacol. 2018, 175, 1039–1053. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  109. Gaillard, D.; Xu, M.; Liu, F.; Millar, S.E.; Barlow, L.A. β-Catenin Signaling Biases Multipotent Lingual Epithelial Progenitors to Differentiate and Acquire Specific Taste Cell Fates. PLoS Genet. 2015, 11, e1005208. [Google Scholar] [CrossRef] [PubMed]
  110. Lawton, D.M.; Furness, D.N.; Lindemann, B.; Hackney, C.M. Localization of the glutamate-aspartate transporter, GLAST, in rat taste buds. Eur. J. Neurosci. 2000, 12, 3163–3171. [Google Scholar] [CrossRef] [PubMed]
  111. Wong, G.T.; Ruiz-Avila, L.; Margolskee, R.F. Directing Gene Expression to Gustducin-Positive Taste Receptor Cells. J. Neurosci. 1999, 19, 5802–5809. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  112. Zhang, Z.; Zhao, Z.; Margolskee, R.; Liman, E. The transduction channel TRPM5 is gated by intracellular calcium in taste cells. J. Neurosci. 2007, 27, 5777–5786. [Google Scholar] [CrossRef] [PubMed]
  113. Clapp, T.R.; Medler, K.F.; Damak, S.; Margolskee, R.F.; Kinnamon, S.C. Mouse taste cells with G protein-coupled taste receptors lack voltage-gated calcium channels and SNAP-25. BMC Biol. 2006, 4, 7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Tomchik, S.M.; Berg, S.; Kim, J.W.; Chaudhari, N.; Roper, S.D. Breadth of tuning and taste coding in mammalian taste buds. J. Neurosci. 2007, 27, 10840–10848. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  115. Beidler, L.M.; Fishman, I.Y.; Hardiman, C.W. Species Differences in Taste Responses. Am. J. Physiol. 1955, 181, 235–239. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  116. Go, Y. Lineage-Specific Expansions and Contractions of the Bitter Taste Receptor Gene Repertoire in Vertebrates. Mol. Biol. Evol. 2006, 23, 964–972. [Google Scholar] [CrossRef] [Green Version]
  117. Hochheimer, A.; Krohn, M.; Rudert, K.; Riedel, K.; Becker, S.; Thirion, C.; Zinke, H. Endogenous gustatory responses and gene expression profile of stably proliferating human taste cells isolated from fungiform papillae. Chem. Senses 2014, 39, 359–377. [Google Scholar] [CrossRef] [Green Version]
  118. Behrens, M.; Meyerhof, W. Bitter taste receptors and human bitter taste perception. Cell. Mol. Life Sci. 2006, 63, 1501–1509. [Google Scholar] [CrossRef]
  119. Li, X.; Li, W.; Wang, H.; Bayley, D.L.; Cao, J.; Reed, D.R.; Bachmanov, A.A.; Huang, L.; Legrand-Defretin, V.; Beauchamp, G.K.; et al. Cats Lack a Sweet Taste Receptor. J. Nutr. 2006, 136, 1932S–1934S. [Google Scholar] [CrossRef] [Green Version]
  120. Jiang, P.; Cui, M.; Zhao, B.; Liu, Z.; Snyder, L.A.; Benard, L.M.J.; Osman, R.; Margolskee, R.F.; Max, M. Lactisole interacts with the transmembrane domains of human T1R3 to inhibit sweet taste. J. Biol. Chem. 2005, 280, 15238–15246. [Google Scholar] [CrossRef] [Green Version]
  121. Inoue, M.; McCaughey, S.A.; Bachmanov, A.A.; Beauchamp, G.K. Whole nerve chorda tympani responses to sweeteners in C57BL/6ByJ and 129P3/J mice. Chem. Senses 2001, 26, 915–923. [Google Scholar] [CrossRef] [Green Version]
  122. Sclafani, A. The sixth taste? Appetite 2004, 43, 1–3. [Google Scholar] [CrossRef]
  123. Sclafani, A.; Zukerman, S.; Glendinning, J.I.; Margolskee, R.F. Fat and carbohydrate preferences in mice: The contribution of alpha-gustducin and Trpm5 taste-signaling proteins. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2007, 293, R1504–R1513. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  124. Barlow, L.A. Progress and renewal in gustation: New insights into taste bud development. Development 2015, 142, 3620–3629. [Google Scholar] [CrossRef] [Green Version]
  125. Ozdener, M.H.; Rawson, N.E. Primary culture of mammalian taste epithelium. Methods Mol. Biol. 2013, 945, 95–107. [Google Scholar] [CrossRef] [Green Version]
  126. Aihara, E.; Mahe, M.M.; Schumacher, M.A.; Matthis, A.L.; Feng, R.; Ren, W.; Noah, T.K.; Matsu-ura, T.; Moore, S.R.; Hong, C.I.; et al. Characterization of stem/progenitor cell cycle using murine circumvallate papilla taste bud organoid. Sci. Rep. 2015, 5, 17185. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  127. Ren, W.; Lewandowski, B.C.; Watson, J.; Aihara, E.; Iwatsuki, K.; Bachmanov, A.A.; Margolskee, R.F.; Jiang, P. Single Lgr5- or Lgr6-expressing taste stem/progenitor cells generate taste bud cells ex vivo. Proc. Natl. Acad. Sci. USA 2014, 111, 16401–16406. [Google Scholar] [CrossRef] [Green Version]
  128. Ren, W.; Aihara, E.; Lei, W.; Gheewala, N.; Uchiyama, H.; Margolskee, R.F.; Iwatsuki, K.; Jiang, P. Transcriptome analyses of taste organoids reveal multiple pathways involved in taste cell generation. Sci. Rep. 2017, 7, 4004. [Google Scholar] [CrossRef] [PubMed]
  129. Wu, C.; Du, L.; Zou, L.; Zhao, L.; Huang, L.; Wang, P. Recent advances in taste cell- and receptor-based biosensors. Sens. Actuators B Chem. 2014, 201, 75–85. [Google Scholar] [CrossRef]
  130. Gee, K.R.; Archer, E.A.; Lapham, L.A.; Leonard, M.E.; Zhou, Z.-L.; Bingham, J.; Diwu, Z. New ratiometric fluorescent calcium indicators with moderately attenuated binding affinities. Bioorganic Med. Chem. Lett. 2000, 10, 1515–1518. [Google Scholar] [CrossRef]
  131. Grynkiewicz, G.; Poenie, M.; Tsien, R.Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J. Biol. Chem. 1985, 260, 3440–3450. [Google Scholar]
  132. Tsien, R.Y.; Rink, T.J.; Poenie, M. Measurement of cytosolic free Ca2+ in individual small cells using fluorescence microscopy with dual excitation wavelengths. Cell Calcium 1985, 6, 145–157. [Google Scholar] [CrossRef]
  133. Akabas, M.H.; Dodd, J.; Al-Awqati, Q. A bitter substance induces a rise in intracellular calcium in a subpopulation of rat taste cells. Science 1988, 242, 1047–1050. [Google Scholar] [CrossRef]
  134. Ogura, T.; Mackay-Sim, A.; Kinnamon, S.C. Bitter Taste Transduction of Denatonium in the Mudpuppy Necturus maculosus. J. Neurosci. 1997, 17, 3580–3587. [Google Scholar] [CrossRef] [Green Version]
  135. Bootman, M.D.; Rietdorf, K.; Collins, T.; Walker, S.; Sanderson, M. Ca2+-sensitive fluorescent dyes and intracellular Ca2+ imaging. Cold Spring Harb. Protoc. 2013, 2013, 83–99. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  136. Di Virgilio, F.; Steinberg, T.H.; Silverstein, S.C. Inhibition of Fura-2 sequestration and secretion with organic anion transport blockers. Cell Calcium 1990, 11, 57–62. [Google Scholar] [CrossRef]
  137. Oakes, S.G.; Martin, W.J.; Lisek, C.A.; Powis, G. Incomplete hydrolysis of the calcium indicator precursor fura-2 pentaacetoxymethyl ester (fura-2 AM) by cells. Anal. Biochem. 1988, 169, 159–166. [Google Scholar] [CrossRef]
  138. Jakob, I.; Hauser, I.A.; Thévenod, F.; Lindemann, B. MDR1 in taste buds of rat vallate papilla: Functional, immunohistochemical, and biochemical evidence. Am. J. Physiol. 1998, 274, C182–C191. [Google Scholar] [CrossRef]
  139. Bernhardt, S.J.; Naim, M.; Zehavi, U.; Lindemann, B. Changes in IP3 and cytosolic Ca2+ in response to sugars and non-sugar sweeteners in transduction of sweet taste in the rat. J. Physiol. (Lond) 1996, 490, 325–336. [Google Scholar] [CrossRef] [PubMed]
  140. Baryshnikov, S.G.; Rogachevskaja, O.A.; Kolesnikov, S.S. Calcium signaling mediated by P2Y receptors in mouse taste cells. J. Neurophysiol. 2003, 90, 3283–3294. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  141. Clapp, T.R.; Trubey, K.R.; Vandenbeuch, A.; Stone, L.M.; Margolskee, R.F.; Chaudhari, N.; Kinnamon, S.C. Tonic activity of Gα-gustducin regulates taste cell responsivity. FEBS Lett. 2008, 582, 3783–3787. [Google Scholar] [CrossRef] [Green Version]
  142. Sinclair, M.S.; Perea-Martinez, I.; Dvoryanchikov, G.; Yoshida, M.; Nishimori, K.; Roper, S.D.; Chaudhari, N. Oxytocin Signaling in Mouse Taste Buds. PLoS ONE 2010, 5, e11980. [Google Scholar] [CrossRef] [Green Version]
  143. Huang, Y.A.; Grant, J.; Roper, S. Glutamate may be an efferent transmitter that elicits inhibition in mouse taste buds. PLoS ONE 2012, 7, e30662. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  144. Kim, Y.V.; Bobkov, Y.V.; Kolesnikov, S.S. Adenosine triphosphate mobilizes cytosolic calcium and modulates ionic currents in mouse taste receptor cells. Neurosci. Lett. 2000, 290, 165–168. [Google Scholar] [CrossRef]
  145. Szebenyi, S.A.; Laskowski, A.I.; Medler, K.F. Sodium/calcium exchangers selectively regulate calcium signaling in mouse taste receptor cells. J. Neurophysiol. 2010, 104, 529–538. [Google Scholar] [CrossRef] [PubMed]
  146. Medler, K.F.; Margolskee, R.F.; Kinnamon, S.C. Electrophysiological Characterization of Voltage-Gated Currents in Defined Taste Cell Types of Mice. J. Neurosci. 2003, 23, 2608–2617. [Google Scholar] [CrossRef]
  147. Herness, S.; Zhao, F.-l.; Kaya, N.; Lu, S.-g.; Shen, T.; Sun, X.-D. Adrenergic signalling between rat taste receptor cells. J. Physiol. (Lond) 2002, 543, 601–614. [Google Scholar] [CrossRef]
  148. Ogura, T.; Kinnamon, S.C. IP(3)-Independent release of Ca(2+) from intracellular stores: A novel mechanism for transduction of bitter stimuli. J. Neurophysiol. 1999, 82, 2657–2666. [Google Scholar] [CrossRef] [PubMed]
  149. Roberts, C.D.; Dvoryanchikov, G.; Roper, S.D.; Chaudhari, N. Interaction between the second messengers cAMP and Ca2+ in mouse presynaptic taste cells. J. Physiol. (Lond) 2009, 587, 1657–1668. [Google Scholar] [CrossRef]
  150. Kawaguchi, H.; Yamanaka, A.; Uchida, K.; Shibasaki, K.; Sokabe, T.; Maruyama, Y.; Yanagawa, Y.; Murakami, S.; Tominaga, M. Activation of Polycystic Kidney Disease-2-like 1 (PKD2L1)-PKD1L3 Complex by Acid in Mouse Taste Cells. J. Biol. Chem. 2010, 285, 17277–17281. [Google Scholar] [CrossRef] [Green Version]
  151. Banik, D.D.; Martin, L.E.; Freichel, M.; Torregrossa, A.-M.; Medler, K.F. TRPM4 and TRPM5 are both required for normal signalling in taste receptor cells. PNAS 2018, 115, E772–E781. [Google Scholar] [CrossRef] [Green Version]
  152. Hayashi, Y.; Zviman, M.M.; Brand, J.G.; Teeter, J.H.; Restrepo, D. Measurement of membrane potential and [Ca2+]i in cell ensembles: Application to the study of glutamate taste in mice. Biophys. J. 1996, 71, 1057–1070. [Google Scholar] [CrossRef] [Green Version]
  153. Wong, S.T.; Henley, J.R.; Kanning, K.C.; Huang, K.-h.; Bothwell, M.; Poo, M.-m. A p75 NTR and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein. Nat. Neurosci. 2002, 5, 1302–1308. [Google Scholar] [CrossRef] [PubMed]
  154. Ishimaru, Y.; Inada, H.; Kubota, M.; Zhuang, H.; Tominaga, M.; Matsunami, H. Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor. Proc. Natl. Acad. Sci. USA 2006, 103, 12569–12574. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  155. Paredes, R.M.; Etzler, J.C.; Watts, L.T.; Lechleiter, J.D. Chemical Calcium Indicators. Methods 2008, 46, 143–151. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  156. Cherkashin, A.P.; Kolesnikova, A.S.; Tarasov, M.V.; Romanov, R.A.; Rogachevskaja, O.A.; Bystrova, M.F.; Kolesnikov, S.S. Expression of calcium-activated chloride channels Ano1 and Ano2 in mouse taste cells. Pflugers Arch-Eur. J. Physiol. 2016, 468, 305–319. [Google Scholar] [CrossRef] [PubMed]
  157. Caicedo, A.; Jafri, M.S.; Roper, S.D. In Situ Ca 2+ Imaging Reveals Neurotransmitter Receptors for Glutamate in Taste Receptor Cells. J. Neurosci. 2000, 20, 7978–7985. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  158. Maruyama, Y.; Pereira, E.; Margolskee, R.F.; Chaudhari, N.; Roper, S.D. Umami responses in mouse taste cells indicate more than one receptor. J. Neurosci. 2006, 26, 2227–2234. [Google Scholar] [CrossRef] [Green Version]
  159. Caicedo, A.; Pereira, E.; Margolskee, R.F.; Roper, S.D. Role of the G-Protein Subunit α-Gustducin in Taste Cell Responses to Bitter Stimuli. J. Neurosci. 2003, 23, 9947–9952. [Google Scholar] [CrossRef] [Green Version]
  160. Richter, T.A.; Dvoryanchikov, G.A.; Chaudhari, N.; Roper, S.D. Acid-sensitive two-pore domain potassium (K2P) channels in mouse taste buds. J. Neurophysiol. 2004, 92, 1928–1936. [Google Scholar] [CrossRef] [Green Version]
  161. Caicedo, A.; Kim, K.-N.; Roper, S.D. Individual mouse taste cells respond to multiple chemical stimuli. J. Physiol. (Lond) 2002, 544, 501–509. [Google Scholar] [CrossRef]
  162. Oheim, M.; Van ‘t Hoff, M.; Feltz, A.; Zamaleeva, A.; Mallet, J.-M.; Collot, M. New red-fluorescent calcium indicators for optogenetics, photoactivation and multi-color imaging. Biochim. Biophys. Acta (BBA)-Mol. Cell Res. 2014, 1843, 2284–2306. [Google Scholar] [CrossRef]
  163. Boens, N.; Qin, W.; Basarić, N.; Orte, A.; Talavera, E.M.; Alvarez-Pez, J.M. Photophysics of the fluorescent pH indicator BCECF. J. Phys. Chem. A 2006, 110, 9334–9343. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  164. Stewart, R.E.; Lyall, V.; Feldman, G.M.; Heck, G.L.; DeSimone, J.A. Acid-induced responses in hamster chorda tympani and intracellular pH tracking by taste receptor cells. Am. J. Physiol. 1998, 275, C227–C238. [Google Scholar] [CrossRef] [PubMed]
  165. Trubey, K.R.; Culpepper, S.; Maruyama, Y.; Kinnamon, S.C.; Chaudhari, N. Tastants evoke cAMP signal in taste buds that is independent of calcium signaling. Am. J. Physiol. Cell Physiol. 2006, 291, C237–C244. [Google Scholar] [CrossRef] [PubMed]
  166. Liu, L.; Simon, S.A. Acidic stimuli activates two distinct pathways in taste receptor cells from rat fungiform papillae. Brain Res. 2001, 923, 58–70. [Google Scholar] [CrossRef]
  167. Hayato, R.; Ohtubo, Y.; Yoshii, K. Functional expression of ionotropic purinergic receptors on mouse taste bud cells. J. Physiol. (Lond) 2007, 584, 473–488. [Google Scholar] [CrossRef] [Green Version]
  168. Rebello, M.R.; Maliphol, A.B.; Medler, K.F. Ryanodine Receptors Selectively Interact with L Type Calcium Channels in Mouse Taste Cells. PLoS ONE 2013, 8, e68174. [Google Scholar] [CrossRef] [Green Version]
  169. Rebello, M.R.; Maliphol A., B.; Medler, K.F. Ryanodine Receptors Selectively Interact with L Type Calcium Channels in Mouse Taste Cells. PLoS ONE 2013, 8, e68174. [Google Scholar] [CrossRef] [Green Version]
  170. Laskowski, A.I.; Medler, K.F. Sodium-calcium exchangers contribute to the regulation of cytosolic calcium levels in mouse taste cells. J. Physiol. (Lond) 2009, 587, 4077–4089. [Google Scholar] [CrossRef]
  171. Ogura, T.; Margolskee, R.F.; Kinnamon, S.C. Taste receptor cell responses to the bitter stimulus denatonium involve Ca2+ influx via store-operated channels. J. Neurophysiol. 2002, 87, 3152–3155. [Google Scholar] [CrossRef] [Green Version]
  172. Kudo, K.-i.; Kawabata, F.; Nomura, T.; Aridome, A.; Nishimura, S.; Tabata, S. Isolation of chicken taste buds for real-time Ca2+ imaging. Anim. Sci. J. 2014, 85, 904–909. [Google Scholar] [CrossRef] [PubMed]
  173. Whitaker, M. Genetically encoded probes for measurement of intracellular calcium. Methods Cell Biol. 2010, 99, 153–182. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  174. Mank, M.; Griesbeck, O. Genetically encoded calcium indicators. Chem. Rev. 2008, 108, 1550–1564. [Google Scholar] [CrossRef] [PubMed]
  175. Zhong, C.; Schleifenbaum, J. Genetically Encoded Calcium Indicators: A New Tool in Renal Hypertension Research. Front. Med. (Lausanne) 2019, 6, 128. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  176. Pérez Koldenkova, V.; Nagai, T. Genetically encoded Ca2+ indicators: Properties and evaluation. Biochim. Biophys. Acta (BBA)-Mol. Cell Res. 2013, 1833, 1787–1797. [Google Scholar] [CrossRef] [Green Version]
  177. SHIMOMURA, O.; JOHNSON, F.H.; SAIGA, Y. Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea. J. Cell. Comp. Physiol. 1962, 59, 223–239. [Google Scholar] [CrossRef]
  178. Chalfie, M.; Tu, Y.; Euskirchen, G.; Ward, W.W.; Prasher, D.C. Green fluorescent protein as a marker for gene expression. Science 1994, 263, 802–805. [Google Scholar] [CrossRef] [Green Version]
  179. Von Molitor, E.; Nürnberg, E.; Ertongur-Fauth, T.; Scholz, P.; Riedel, K.; Hafner, M.; Rudolf, R.; Cesetti, T. Analysis of Calcium Signaling in Live Human Tongue Cell 3D-Cultures upon Tastant Perfusion. Cell Calcium 2020, 102164. [Google Scholar] [CrossRef]
  180. Kim, Y.S.; Chu, Y.; Han, L.; Li, M.; Li, Z.; LaVinka, P.C.; Sun, S.; Tang, Z.; Park, K.; Caterina, M.J.; et al. Central Terminal Sensitization of TRPV1 by Descending Serotonergic Facilitation Modulates Chronic Pain. Neuron 2014, 81, 873–887. [Google Scholar] [CrossRef] [Green Version]
  181. Kim, Y.S.; Anderson, M.; Park, K.; Zheng, Q.; Agarwal, A.; Gong, C.; Saijilafu; Young, L.; He, S.; LaVinka, P.C.; et al. Coupled Activation of Primary Sensory Neurons Contributes to Chronic Pain. Neuron 2016, 91, 1085–1096. [Google Scholar] [CrossRef] [Green Version]
  182. Rink, T.J.; Tsien, R.Y.; Pozzan, T. Cytoplasmic pH and free Mg2+ in lymphocytes. J. Cell Biol. 1982, 95, 189–196. [Google Scholar] [CrossRef] [Green Version]
  183. Lyall, V.; Alam, R.I.; Phan, T.-H.T.; Russell, O.F.; Malik, S.A.; Heck, G.L.; Desimone, J.A. Modulation of Rat Chorda Tympani NaCl Responses and Intracellular Na+ Activity in Polarized Taste Receptor Cells by pH. J. Gen. Physiol. 2002, 120, 793–815. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  184. Bachmanov, A.A.; Tordoff, M.G.; Beauchamp, G.K. Ethanol Consumption and Taste Preferences in C57BL/6ByJ and 129/J Mice. Alcohol. Clin. Exp. Res. 1996, 20, 201–206. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  185. Tu, Y.-H.; Cooper, A.J.; Teng, B.; Chang, R.B.; Artiga, D.J.; Turner, H.N.; Mulhall, E.M.; Ye, W.; Smith, A.D.; Liman, E.R. An evolutionarily conserved gene family encodes proton-selective ion channels. Science 2018, 359, 1047–1050. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  186. Hamilton, R.B.; Norgren, R. Central projections of gustatory nerves in the rat. J. Comp. Neurol. 1984, 222, 560–577. [Google Scholar] [CrossRef]
  187. Ohla, K.; Yoshida, R.; Roper, S.D.; Di Lorenzo, P.M.; Victor, J.D.; Boughter, J.D.; Fletcher, M.; Katz, D.B.; Chaudhari, N. Recognizing Taste: Coding Patterns Along the Neural Axis in Mammals. Chem. Senses 2019, 44, 237–247. [Google Scholar] [CrossRef]
  188. Gutierrez, R.; Simon, S.A. Chemosensory processing in the taste-reward pathway. Flavour Fragr. J. 2011, 26, 231–238. [Google Scholar] [CrossRef] [Green Version]
  189. Carleton, A.; Accolla, R.; Simon, S.A. Coding in the mammalian gustatory system. Trends Neurosci. 2010, 33, 326–334. [Google Scholar] [CrossRef] [Green Version]
  190. Lemon, C.H.; Katz, D.B. The neural processing of taste. BMC Neurosci. 2007, 8 (Suppl. 3), S5. [Google Scholar] [CrossRef] [Green Version]
  191. Simon, S.A.; Araujo, I.E.d.; Gutierrez, R.; Nicolelis, M.A.L. The neural mechanisms of gustation: A distributed processing code. Nat. Rev. Neurosci. 2006, 7, 890–901. [Google Scholar] [CrossRef]
  192. Fletcher, M.L.; Ogg, M.C.; Lu, L.; Ogg, R.J.; Boughter, J.D. Overlapping Representation of Primary Tastes in a Defined Region of the Gustatory Cortex. J. Neurosci. 2017, 37, 7595–7605. [Google Scholar] [CrossRef] [Green Version]
  193. Chen, X.; Gabitto, M.; Peng, Y.; Ryba, N.J.P.; Zuker, C.S. A gustotopic map of taste qualities in the mammalian brain. Science 2011, 333, 1262–1266. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  194. Prinster, A.; Cantone, E.; Verlezza, V.; Magliulo, M.; Sarnelli, G.; Iengo, M.; Cuomo, R.; Di Salle, F.; Esposito, F. Cortical representation of different taste modalities on the gustatory cortex: A pilot study. PLoS ONE 2017, 12, e0190164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  195. Chikazoe, J.; Lee, D.H.; Kriegeskorte, N.; Anderson, A.K. Distinct representations of basic taste qualities in human gustatory cortex. Nat. Commun. 2019, 10, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  196. Yoshimura, H.; Sugai, T.; Fukuda, M.; Segami, N.; Onoda, N. Cortical spatial aspects of optical intrinsic signals in response to sucrose and NaCl stimuli. Neuroreport 2004, 15, 17–20. [Google Scholar] [CrossRef]
  197. Accolla, R.; Bathellier, B.; Petersen, C.C.H.; Carleton, A. Differential spatial representation of taste modalities in the rat gustatory cortex. J. Neurosci. 2007, 27, 1396–1404. [Google Scholar] [CrossRef] [Green Version]
  198. Ali, F.; Kwan, A.C. Interpreting in vivo calcium signals from neuronal cell bodies, axons, and dendrites: A review. Neurophotonics 2020, 7, 11402. [Google Scholar] [CrossRef]
  199. Lentz, T.B.; Gray, S.J.; Samulski, R.J. Viral vectors for gene delivery to the central nervous system. Neurobiol. Dis. 2012, 48, 179–188. [Google Scholar] [CrossRef] [Green Version]
  200. Hammond, S.L.; Leek, A.N.; Richman, E.H.; Tjalkens, R.B. Cellular selectivity of AAV serotypes for gene delivery in neurons and astrocytes by neonatal intracerebroventricular injection. PLoS ONE 2017, 12, e0188830. [Google Scholar] [CrossRef] [Green Version]
  201. Barretto, R.P.J.; Gillis-Smith, S.; Chandrashekar, J.; Yarmolinsky, D.A.; Schnitzer, M.J.; Ryba, N.J.P.; Zuker, C.S. The neural representation of taste quality at the periphery. Nature 2015, 517, 373–376. [Google Scholar] [CrossRef] [Green Version]
  202. Chen, T.-W.; Wardill, T.J.; Sun, Y.; Pulver, S.R.; Renninger, S.L.; Baohan, A.; Schreiter, E.R.; Kerr, R.A.; Orger, M.B.; Jayaraman, V.; et al. Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature 2013, 499, 295–300. [Google Scholar] [CrossRef] [Green Version]
  203. Sahu, P.; Mazumder, N. Advances in adaptive optics–based two-photon fluorescence microscopy for brain imaging. Lasers Med. Sci. 2020, 35, 317–328. [Google Scholar] [CrossRef] [PubMed]
  204. Lecoq, J.; Orlova, N.; Grewe, B.F. Wide. Fast. Deep: Recent Advances in Multiphoton Microscopy of In Vivo Neuronal Activity. J. Neurosci. 2019, 39, 9042–9052. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  205. Wu, A.; Dvoryanchikov, G.; Pereira, E.; Chaudhari, N.; Roper, S.D. Breadth of tuning in taste afferent neurons varies with stimulus strength. Nat. Commun. 2015, 6, 8171. [Google Scholar] [CrossRef] [Green Version]
  206. Sugita, M.; Yamamoto, K.; Hirono, C.; Shiba, Y. Information processing in brainstem bitter taste-relaying neurons defined by genetic tracing. Neuroscience 2013, 250, 166–180. [Google Scholar] [CrossRef] [PubMed]
  207. Lavi, K.; Jacobson, G.A.; Rosenblum, K.; Lüthi, A. Encoding of Conditioned Taste Aversion in Cortico-Amygdala Circuits. Cell Rep. 2018, 24, 278–283. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  208. Fu, O.; Iwai, Y.; Kondoh, K.; Misaka, T.; Minokoshi, Y.; Nakajima, K.-I. SatB2-Expressing Neurons in the Parabrachial Nucleus Encode Sweet Taste. Cell Rep. 2019, 27, 1650–1656.e4. [Google Scholar] [CrossRef] [Green Version]
  209. Susaki, E.A.; Tainaka, K.; Perrin, D.; Yukinaga, H.; Kuno, A.; Ueda, H.R. Advanced CUBIC protocols for whole-brain and whole-body clearing and imaging. Nat. Protoc. 2015, 10, 1709–1727. [Google Scholar] [CrossRef] [Green Version]
  210. Lemon, C.H. Perceptual and Neural Responses to Sweet Taste in Humans and Rodents. Chem. Percept. 2015, 8, 46–52. [Google Scholar] [CrossRef] [Green Version]
  211. Rolls, E.T. Brain mechanisms underlying flavour and appetite. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2006, 361, 1123–1136. [Google Scholar] [CrossRef] [Green Version]
  212. Kobayashi, M. Functional Organization of the Human Gustatory Cortex. J. Oral Biosci. 2006, 48, 244–260. [Google Scholar] [CrossRef]
  213. Vendrell-Llopis, N.; Yaksi, E. Evolutionary conserved brainstem circuits encode category, concentration and mixtures of taste. Sci. Rep. 2015, 5, 17825. [Google Scholar] [CrossRef] [Green Version]
  214. Vandenbeuch, A.; Kinnamon, S.C. Why do taste cells generate action potentials? J. Biol. 2009, 8, 42. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  215. Roper, S. Regenerative impulses in taste cells. Science 1983, 220, 1311–1312. [Google Scholar] [CrossRef]
  216. Kinnamon, S.C.; Roper, S.D. Passive and active membrane properties of mudpuppy taste receptor cells. J. Physiol. (Lond) 1987, 383, 601–614. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  217. Cummings, T.A.; Daniels, C.; Kinnamon, S.C. Sweet taste transduction in hamster: Sweeteners and cyclic nucleotides depolarize taste cells by reducing a K+ current. J. Neurophysiol. 1996, 75, 1256–1263. [Google Scholar] [CrossRef] [PubMed]
  218. Avenet, P.; Lindemann, B. Noninvasive recording of receptor cell action potentials and sustained currents from single taste buds maintained in the tongue: The response to mucosal NaCl and amiloride. J. Membrain Biol. 1991, 124, 33–41. [Google Scholar] [CrossRef]
  219. Furue, H.; Yoshii, K. In situ tight-seal recordings of taste substance-elicited action currents and voltage-gated Ba currents from single taste bud cells in the peeled epithelium of mouse tongue. Brain Res. 1997, 776, 133–139. [Google Scholar] [CrossRef]
  220. Chen, Y.; Sun, X.D.; Herness, S. Characteristics of action potentials and their underlying outward currents in rat taste receptor cells. J. Neurophysiol. 1996, 75, 820–831. [Google Scholar] [CrossRef]
  221. Herness, M.S.; Sun, X.-D. Voltage-dependent sodium currents recorded from dissociated rat taste cells. J. Membarin Biol. 1995, 146, 73–84. [Google Scholar] [CrossRef]
  222. Noguchi, T.; Ikeda, Y.; Miyajima, M.; Yoshii, K. Voltage-gated channels involved in taste responses and characterizing taste bud cells in mouse soft palates. Brain Res. 2003, 982, 241–259. [Google Scholar] [CrossRef]
  223. Varkevisser, B.; Peterson, D.; Ogura, T.; Kinnamon, S.C. Neural networks distinguish between taste qualities based on receptor cell population responses. Chem Senses 2001, 26, 499–505. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  224. Yoshida, R.; Shigemura, N.; Sanematsu, K.; Yasumatsu, K.; Ishizuka, S.; Ninomiya, Y. Taste responsiveness of fungiform taste cells with action potentials. J. Neurophysiol. 2006, 96, 3088–3095. [Google Scholar] [CrossRef] [Green Version]
  225. DAVILA, H.V.; SALZBERG, B.M.; COHEN, L.B.; WAGGONER, A.S. A Large Change in Axon Fluorescence that Provides a Promising Method for Measuring Membrane Potential. Nat. New Biol. 1973, 241, 159–160. [Google Scholar] [CrossRef]
  226. Xu, Y.; Zou, P.; Cohen, A.E. Voltage imaging with genetically encoded indicators. Curr. Opin. Chem. Biol. 2017, 39, 1–10. [Google Scholar] [CrossRef] [PubMed]
  227. Antic, S.D.; Empson, R.M.; Knöpfel, T. Voltage imaging to understand connections and functions of neuronal circuits. J. Neurophysiol. 2016, 116, 135–152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  228. Preuss, S.; Stein, W. Comparison of Two Voltage-Sensitive Dyes and Their Suitability for Long-Term Imaging of Neuronal Activity. PLoS ONE 2013, 8. [Google Scholar] [CrossRef] [Green Version]
  229. Fluhler, E.; Burnham, V.G.; Loew, L.M. Spectra, membrane binding, and potentiometric responses of new charge shift probes. Biochemistry 1985, 24, 5749–5755. [Google Scholar] [CrossRef]
  230. Loew, L.M.; Simpson, L.L. Charge-shift probes of membrane potential: A probable electrochromic mechanism for p-aminostyrylpyridinium probes on a hemispherical lipid bilayer. Biophys. J. 1981, 34, 353–365. [Google Scholar] [CrossRef] [Green Version]
  231. Li, J.H.-Y.; Lindemann, B. Multi-photon microscopy of cell types in the viable taste disk of the frog. Cell Tissue Res. 2003, 313, 11–27. [Google Scholar] [CrossRef]
  232. Loew, L.M. Potentiometric dyes: Imaging electrical activity of cell membranes. Pure Appl. Chem. 1996, 68, 1405–1409. [Google Scholar] [CrossRef]
  233. Bachtel, A.D.; Gray, R.A.; Stohlman, J.M.; Bourgeois, E.B.; Pollard, A.E.; Rogers, J.M. A novel approach to dual excitation ratiometric optical mapping of cardiac action potentials with di-4-ANEPPS using pulsed LED excitation. IEEE Trans. Biomed. Eng. 2011, 58, 2120–2126. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  234. Vitha, M.F.; Clarke, R.J. Comparison of excitation and emission ratiometric fluorescence methods for quantifying the membrane dipole potential. Biochim. Biophys. Acta (BBA) Biomembr. 2007, 1768, 107–114. [Google Scholar] [CrossRef] [Green Version]
  235. Canepari, M.; Vogt, K.; Zecevic, D. Combining Voltage and Calcium Imaging from Neuronal Dendrites. Cell Mol. Neurobiol. 2008, 28, 1079–1093. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  236. Ehrenberg, B.; Montana, V.; Wei, M.D.; Wuskell, J.P.; Loew, L.M. Membrane potential can be determined in individual cells from the nernstian distribution of cationic dyes. Biophys. J. 1988, 53, 785–794. [Google Scholar] [CrossRef] [Green Version]
  237. Scaduto, R.C.; Grotyohann, L.W. Measurement of Mitochondrial Membrane Potential Using Fluorescent Rhodamine Derivatives. Biophys. J. 1999, 76, 469–477. [Google Scholar] [CrossRef] [Green Version]
  238. Ohtubo, Y.; Suemitsu, T.; Shiobara, S.; Matsumoto, T.; Kumazawa, T.; Yoshii, K.Y. Optical recordings of taste responses from fungiform papillae of mouse in situ. J. Physiol. (Lond) 2001, 530, 287–293. [Google Scholar] [CrossRef] [PubMed]
  239. Yang, H.H.; St-Pierre, F.; Sun, X.; Ding, X.; Lin, M.Z.; Clandinin, T.R. Subcellular Imaging of Voltage and Calcium Signals Reveals Neural Processing In Vivo. Cell 2016, 166, 245–257. [Google Scholar] [CrossRef] [Green Version]
  240. Bando, Y.; Grimm, C.; Cornejo, V.H.; Yuste, R. Genetic voltage indicators. BMC Biol. 2019, 17, 1–12. [Google Scholar] [CrossRef]
  241. Abdelfattah, A.S.; Kawashima, T.; Singh, A.; Novak, O.; Liu, H.; Shuai, Y.; Huang, Y.-C.; Campagnola, L.; Seeman, S.C.; Yu, J.; et al. Bright and photostable chemigenetic indicators for extended in vivo voltage imaging. Science 2019, 365, 699–704. [Google Scholar] [CrossRef] [PubMed]
  242. Abdelfattah, A.S.; Farhi, S.L.; Zhao, Y.; Brinks, D.; Zou, P.; Ruangkittisakul, A.; Platisa, J.; Pieribone, V.A.; Ballanyi, K.; Cohen, A.E.; et al. A Bright and Fast Red Fluorescent Protein Voltage Indicator That Reports Neuronal Activity in Organotypic Brain Slices. J. Neurosci. 2016, 36, 2458–2472. [Google Scholar] [CrossRef]
  243. Quicke, P.; Song, C.; McKimm, E.J.; Milosevic, M.M.; Howe, C.L.; Neil, M.; Schultz, S.R.; Antic, S.D.; Foust, A.J.; Knöpfel, T. Single-Neuron Level One-Photon Voltage Imaging With Sparsely Targeted Genetically Encoded Voltage Indicators. Front. Cell. Neurosci. 2019, 13, 39. [Google Scholar] [CrossRef] [PubMed]
  244. Beck, C.; Gong, Y. A high-speed, bright, red fluorescent voltage sensor to detect neural activity. Sci. Rep. 2019, 9, 15878. [Google Scholar] [CrossRef] [PubMed]
  245. Sugai, T.; Yamamoto, R.; Yoshimura, H.; Kato, N. Multimodal Cross-Talk of Olfactory and Gustatory Information in the Endopiriform Nucleus in Rats. Chem Senses 2012, 37, 681–688. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  246. Margolskee, R.F. The biochemistry and molecular biology of taste transduction. Curr. Opin. Neurobiol. 1993, 3, 526–531. [Google Scholar] [CrossRef]
  247. Eric Walters, D. How are bitter and sweet tastes related? Trends Food Sci. Technol. 1996, 7, 399–403. [Google Scholar] [CrossRef]
  248. Kolesnikov, S.S.; Margolskee, R.F. A cyclic-nucleotide-suppressible conductance activated by transducin in taste cells. Nature 1995, 376, 85–88. [Google Scholar] [CrossRef]
  249. Misaka, T.; Kusakabe, Y.; Emori, Y.; Gonoi, T.; Arai, S.; Abe, K. Taste buds have a cyclic nucleotide-activated channel, CNGgust. J. Biol. Chem. 1997, 272, 22623–22629. [Google Scholar] [CrossRef] [Green Version]
  250. Adams, S.R.; Harootunian, A.T.; Buechler, Y.J.; Taylor, S.S.; Tsien, R.Y. Fluorescence ratio imaging of cyclic AMP in single cells. Nature 1991, 349, 694–697. [Google Scholar] [CrossRef]
  251. Patel, N.; Gold, M.G. The genetically encoded tool set for investigating cAMP: More than the sum of its parts. Front. Pharmacol. 2015, 6, 164. [Google Scholar] [CrossRef] [Green Version]
  252. Zaccolo, M.; Giorgi, F.D.; Cho, C.Y.; Feng, L.; Knapp, T.; Negulescu, P.A.; Taylor, S.S.; Tsien, R.Y.; Pozzan, T. A genetically encoded, fluorescent indicator for cyclic AMP in living cells. Nat. Cell Biol. 2000, 2, 25–29. [Google Scholar] [CrossRef] [Green Version]
  253. Zaccolo, M. Use of chimeric fluorescent proteins and fluorescence resonance energy transfer to monitor cellular responses. Circ. Res. 2004, 94, 866–873. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  254. Jiang, J.Y.; Falcone, J.L.; Curci, S.; Hofer, A.M. Interrogating cyclic AMP signaling using optical approaches. Cell Calcium 2017, 64, 47–56. [Google Scholar] [CrossRef] [PubMed]
  255. Zaccolo, M.; Musheshe, N.; Lobo, M.J.; Schmidt, M. Targeting FRET-based reporters for cAMP and PKA activity using AKAP79. Sensors 2018, 18, E2164. [Google Scholar]
  256. Rudolf, R.; Magalhães, P.J.; Pozzan, T. Direct in vivo monitoring of sarcoplasmic reticulum Ca2+ and cytosolic cAMP dynamics in mouse skeletal muscle. J Cell Biol 2006, 173, 187–193. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  257. Buck, M.A.; Fraser, C.M. Muscarinic acetylcholine receptor subtypes which selectively couple to phospholipase C: Pharmacological and biochemical properties. Biochem. Biophys. Res. Commun. 1990, 173, 666–672. [Google Scholar] [CrossRef]
  258. Bhuckory, S.; Kays, J.C.; Dennis, A.M. In Vivo Biosensing Using Resonance Energy Transfer. Biosensors (Basel) 2019, 9, 76. [Google Scholar] [CrossRef] [Green Version]
  259. Ueda, T.; Ugawa, S.; Yamamura, H.; Imaizumi, Y.; Shimada, S. Functional Interaction between T2R Taste Receptors and G-Protein α Subunits Expressed in Taste Receptor Cells. J. Neurosci. 2003, 23, 7376–7380. [Google Scholar] [CrossRef] [Green Version]
  260. Ishii, S.; Misaka, T.; Kishi, M.; Kaga, T.; Ishimaru, Y.; Abe, K. Acetic acid activates PKD1L3–PKD2L1 channel—A candidate sour taste receptor. Biochem. Biophys. Res. Commun. 2009, 385, 346–350. [Google Scholar] [CrossRef]
  261. Riera, C.E.; Vogel, H.; Simon, S.A.; Le Coutre, J. Artificial sweeteners and salts producing a metallic taste sensation activate TRPV1 receptors. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2007, 293, R626–R634. [Google Scholar] [CrossRef] [Green Version]
  262. Pérez, C.A.; Huang, L.; Rong, M.; Kozak, J.A.; Preuss, A.K.; Zhang, H.; Max, M.; Margolskee, R.F. A transient receptor potential channel expressed in taste receptor cells. Nat. Neurosci. 2002, 5, 1169–1176. [Google Scholar] [CrossRef]
  263. Medina, J.; Nakagawa, Y.; Nagasawa, M.; Fernandez, A.; Sakaguchi, K.; Kitaguchi, T.; Kojima, I. Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose. J. Biol. Chem. 2016, 291, 23126–23135. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  264. Fujimoto, C.; Ishimaru, Y.; Katano, Y.; Misaka, T.; Yamasoba, T.; Asakura, T.; Abe, K. The single pore residue Asp523 in PKD2L1 determines Ca2+ permeation of the PKD1L3/PKD2L1 complex. Biochem. Biophys. Res. Commun. 2011, 404, 946–951. [Google Scholar] [CrossRef] [PubMed]
  265. Brockhoff, A.; Behrens, M.; Niv, M.Y.; Meyerhof, W. Structural requirements of bitter taste receptor activation. Proc. Natl. Acad. Sci. USA 2010, 107, 11110–11115. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  266. Jiang, P.; Cui, M.; Zhao, B.; Snyder, L.A.; Benard, L.M.J.; Osman, R.; Max, M.; Margolskee, R.F. Identification of the cyclamate interaction site within the transmembrane domain of the human sweet taste receptor subunit T1R3. J. Biol. Chem. 2005, 280, 34296–34305. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  267. Gee, K.R.; Brown, K.A.; Chen, W.-N.U.; Bishop-Stewart, J.; Gray, D.; Johnson, I. Chemical and physiological characterization of fluo-4 Ca2+-indicator dyes. Cell Calcium 2000, 27, 97–106. [Google Scholar] [CrossRef]
  268. Offermanns, S.; Simon, M.I. G alpha 15 and G alpha 16 couple a wide variety of receptors to phospholipase C. J. Biol. Chem. 1995, 270, 15175–15180. [Google Scholar] [CrossRef] [Green Version]
  269. Krautwurst, D.; Yau, K.-W.; Reed, R.R. Identification of Ligands for Olfactory Receptors by Functional Expression of a Receptor Library. Cell 1998, 95, 917–926. [Google Scholar] [CrossRef] [Green Version]
  270. Brockhoff, A.; Behrens, M.; Roudnitzky, N.; Appendino, G.; Avonto, C.; Meyerhof, W. Receptor agonism and antagonism of dietary bitter compounds. J. Neurosci. 2011, 31, 14775–14782. [Google Scholar] [CrossRef] [Green Version]
  271. Behrens, M.; Blank, K.; Meyerhof, W. Blends of Non-caloric Sweeteners Saccharin and Cyclamate Show Reduced Off-Taste due to TAS2R Bitter Receptor Inhibition. Cell Chem. Biol. 2017, 24, 1199–1204.e2. [Google Scholar] [CrossRef] [Green Version]
  272. McLaughlin, S.K.; McKinnon, P.J.; Margolskee, R.F. Gustducin is a taste-cell-specific G protein closely related to the transducins. Nature 1992, 357, 563–569. [Google Scholar] [CrossRef] [PubMed]
  273. McLaughlin, S.K.; McKinnon, P.J.; Robichon, A.; Spickofsky, N.; Margolskee, R.F. Gustducin and transducin: A tale of two G proteins. Ciba Found. Symp. 1993, 179, 186–200. [Google Scholar] [CrossRef] [PubMed]
  274. Kusakabe, Y.; Yasuoka, A.; Asano-Miyoshi, M.; Iwabuchi, K.; Matsumoto, I.; Arai, S.; Emori, Y.; Abe, K. Comprehensive study on G protein alpha-subunits in taste bud cells, with special reference to the occurrence of Galphai2 as a major Galpha species. Chem. Senses 2000, 25, 525–531. [Google Scholar] [CrossRef] [PubMed]
  275. Tizzano, M.; Dvoryanchikov, G.; Barrows, J.K.; Kim, S.; Chaudhari, N.; Finger, T.E. Expression of Galpha14 in sweet-transducing taste cells of the posterior tongue. BMC Neurosci. 2008, 9, 110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  276. Soranzo, N.; Bufe, B.; Sabeti, P.C.; Wilson, J.F.; Weale, M.E.; Marguerie, R.; Meyerhof, W.; Goldstein, D.B. Positive Selection on a High-Sensitivity Allele of the Human Bitter-Taste Receptor TAS2R16. Curr. Biol. 2005, 15, 1257–1265. [Google Scholar] [CrossRef] [Green Version]
  277. Bolsover, S.; Ibrahim, O.; O’luanaigh, N.; Williams, H.; Cockcroft, S. Use of fluorescent Ca2+ dyes with green fluorescent protein and its variants: Problems and solutions. Biochem. J. 2001, 356, 345–352. [Google Scholar] [CrossRef]
  278. Schreder, B.; Lukacs, Z.; Schmitt, M.; Schreier, P.; Humpf, H.-U. 1-Naphthoic acid: A new type of asymmetric chromophore for exciton-coupled circular dichroism (ECCD). Tetrahedron Asymmetry 1996, 7, 1543–1546. [Google Scholar] [CrossRef]
  279. Slack, J.P.; Brockhoff, A.; Batram, C.; Menzel, S.; Sonnabend, C.; Born, S.; Galindo, M.M.; Kohl, S.; Thalmann, S.; Ostopovici-Halip, L.; et al. Modulation of bitter taste perception by a small molecule hTAS2R antagonist. Curr. Biol. 2010, 20, 1104–1109. [Google Scholar] [CrossRef] [Green Version]
  280. Servant, G.; Brust, P.; Ray, S.; Hung, N. Cell-Based Fluorescent Assays for Identifying Alpha and Delta ENaC Modulators. Google Patents US20090181404A1, 16 July 2009. [Google Scholar]
  281. Callamaras, N.; Chang, H. High throughput cell-based assay for monitoring sodium channel activity and discovery of salty taste modulating compounds. Google Patents AU 2002308481A8, 1 February 2007. [Google Scholar]
  282. Landin, A.M.; Kim, J.W.; Chaudhari, N. Liposome-mediated transfection of mature taste cells. J. Neurobiol. 2005, 65, 12–21. [Google Scholar] [CrossRef]
  283. Kishi, M.; Emori, Y.; Tsukamoto, Y.; Abe, K. Primary culture of rat taste bud cells that retain molecular markers for taste buds and permit functional expression of foreign genes. Neuroscience 2001, 106, 217–225. [Google Scholar] [CrossRef]
  284. Cavnar, S.P.; Salomonsson, E.; Luker, K.E.; Luker, G.D.; Takayama, S. Transfer, imaging, and analysis plate for facile handling of 384 hanging drop 3D tissue spheroids. J. Lab. Autom. 2014, 19, 208–214. [Google Scholar] [CrossRef] [Green Version]
  285. Costa, E.C.; Gaspar, V.M.; Coutinho, P.; Correia, I.J. Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models. Biotechnol. Bioeng. 2014, 111, 1672–1685. [Google Scholar] [CrossRef] [PubMed]
  286. Gualda, E.J.; Simão, D.; Pinto, C.; Alves, P.M.; Brito, C. Imaging of human differentiated 3D neural aggregates using light sheet fluorescence microscopy. Front. Cell. Neurosci. 2014, 8, 221. [Google Scholar] [CrossRef] [PubMed]
  287. Foster, S.R.; Roura, E.; Thomas, W.G. Extrasensory perception: Odorant and taste receptors beyond the nose and mouth. Pharmacol. Ther. 2014, 142, 41–61. [Google Scholar] [CrossRef]
  288. Brockhoff, A.; Behrens, M.; Massarotti, A.; Appendino, G.; Meyerhof, W. Broad tuning of the human bitter taste receptor hTAS2R46 to various sesquiterpene lactones, clerodane and labdane diterpenoids, strychnine, and denatonium. J. Agric. Food Chem. 2007, 55, 6236–6243. [Google Scholar] [CrossRef]
  289. Behrens, M.; Brockhoff, A.; Kuhn, C.; Bufe, B.; Winnig, M.; Meyerhof, W. The human taste receptor hTAS2R14 responds to a variety of different bitter compounds. Biochem. Biophys. Res. Commun. 2004, 319, 479–485. [Google Scholar] [CrossRef]
  290. Behrens, M.; Brockhoff, A.; Batram, C.; Kuhn, C.; Appendino, G.; Meyerhof, W. The human bitter taste receptor hTAS2R50 is activated by the two natural bitter terpenoids andrographolide and amarogentin. J. Agric. Food Chem. 2009, 57, 9860–9866. [Google Scholar] [CrossRef]
  291. Greene, T.A.; Alarcon, S.; Thomas, A.; Berdougo, E.; Doranz, B.J.; Breslin, P.A.S.; Rucker, J.B. Probenecid Inhibits the Human Bitter Taste Receptor TAS2R16 and Suppresses Bitter Perception of Salicin. PLoS ONE 2011, 6. [Google Scholar] [CrossRef]
  292. Bufe, B.; Hofmann, T.; Krautwurst, D.; Raguse, J.-D.; Meyerhof, W. The human TAS2R16 receptor mediates bitter taste in response to beta-glucopyranosides. Nat. Genet. 2002, 32, 397–401. [Google Scholar] [CrossRef]
  293. Xu, H.; Staszewski, L.; Tang, H.; Adler, E.; Zoller, M.; Li, X. Different functional roles of T1R subunits in the heteromeric taste receptors. Proc. Natl. Acad. Sci. USA 2004, 101, 14258–14263. [Google Scholar] [CrossRef] [Green Version]
  294. Galindo-Cuspinera, V.; Winnig, M.; Bufe, B.; Meyerhof, W.; Breslin, P.A.S. A TAS1R receptor-based explanation of sweet ‘water-taste’. Nature 2006, 441, 354–357. [Google Scholar] [CrossRef]
  295. Haruyama, N.; Cho, A.; Kulkarni, A.B. Overview: Engineering transgenic constructs and mice. Curr. Protoc. Cell Biol. 2009, 19, 19.10.1-19.10.9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  296. Li, S.; Chen, L.-X.; Peng, X.-H.; Wang, C.; Qin, B.-Y.; Tan, D.; Han, C.-X.; Yang, H.; Ren, X.-N.; Liu, F.; et al. Overview of the reporter genes and reporter mouse models. Animal Model. Exp. Med. 2018, 1, 29–35. [Google Scholar] [CrossRef] [PubMed]
  297. Kim, J.W.; Roberts, C.; Maruyama, Y.; Berg, S.; Roper, S.; Chaudhari, N. Faithful expression of GFP from the PLCbeta2 promoter in a functional class of taste receptor cells. Chem. Senses 2006, 31, 213–219. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  298. Chattopadhyaya, B.; Di Cristo, G.; Higashiyama, H.; Knott, G.W.; Kuhlman, S.J.; Welker, E.; Huang, Z.J. Experience and Activity-Dependent Maturation of Perisomatic GABAergic Innervation in Primary Visual Cortex during a Postnatal Critical Period. J. Neurosci. 2004, 24, 9598–9611. [Google Scholar] [CrossRef] [PubMed]
  299. Tamura, T.-a.; Hashimoto, M.; Aruga, J.; Konishi, Y.; Nakagawa, M.; Ohbayashi, T.; Shimada, M.; Mikoshiba, K. Promoter structure and gene expression of the mouse inositol 1,4,5-trisphosphate receptor type 3 gene. Gene 2001, 275, 169–176. [Google Scholar] [CrossRef]
  300. Damak, S.; Mosinger, B.; Margolskee, R.F. Transsynaptic transport of wheat germ agglutinin expressed in a subset of type II taste cells of transgenic mice. BMC Neurosci. 2008, 9, 96. [Google Scholar] [CrossRef] [Green Version]
  301. Vandenbeuch, A.; Clapp, T.R.; Kinnamon, S.C. Amiloride-sensitive channels in type I fungiform taste cells in mouse. BMC Neurosci. 2008, 9, 1. [Google Scholar] [CrossRef]
  302. Feng, P.; Zhao, H.; Chai, J.; Huang, L.; Wang, H. Expression and secretion of TNF-α in mouse taste buds: A novel function of a specific subset of type II taste cells. PLoS ONE 2012, 7, e43140. [Google Scholar] [CrossRef] [Green Version]
  303. Parker, M.R.; Feng, D.; Chamuris, B.; Margolskee, R.F. Expression and nuclear translocation of glucocorticoid receptors in type 2 taste receptor cells. Neurosci. Lett. 2014, 571, 72–77. [Google Scholar] [CrossRef] [Green Version]
  304. Takai, S.; Yasumatsu, K.; Inoue, M.; Iwata, S.; Yoshida, R.; Shigemura, N.; Yanagawa, Y.; Drucker, D.J.; Margolskee, R.F.; Ninomiya, Y. Glucagon-like peptide-1 is specifically involved in sweet taste transmission. FASEB J. 2015, 29, 2268–2280. [Google Scholar] [CrossRef] [Green Version]
  305. Yoshida, R.; Noguchi, K.; Shigemura, N.; Jyotaki, M.; Takahashi, I.; Margolskee, R.F.; Ninomiya, Y. Leptin suppresses mouse taste cell responses to sweet compounds. Diabetes 2015, 64, 3751–3762. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  306. Mueller, K.L.; Hoon, M.A.; Erlenbach, I.; Chandrashekar, J.; Zuker, C.S.; Ryba, N.J.P. The receptors and coding logic for bitter taste. Nature 2005, 434, 225–229. [Google Scholar] [CrossRef] [PubMed]
  307. Zapata-Hommer, O.; Griesbeck, O. Efficiently folding and circularly permuted variants of the Sapphire mutant of GFP. BMC Biotechnol. 2003, 3, 5. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  308. Yoshida, R.; Miyauchi, A.; Yasuo, T.; Jyotaki, M.; Murata, Y.; Yasumatsu, K.; Shigemura, N.; Yanagawa, Y.; Obata, K.; Ueno, H.; et al. Discrimination of taste qualities among mouse fungiform taste bud cells. J. Physiol. (Lond) 2009, 587, 4425–4439. [Google Scholar] [CrossRef] [PubMed]
  309. Yoshida, R.; Takai, S.; Sanematsu, K.; Margolskee, R.F.; Shigemura, N.; Ninomiya, Y. Bitter Taste Responses of Gustducin-positive Taste Cells in Mouse Fungiform and Circumvallate Papillae. Neuroscience 2018, 369, 29–39. [Google Scholar] [CrossRef]
  310. Dvoryanchikov, G.; Hernandez, D.; Roebber, J.K.; Hill, D.L.; Roper, S.D.; Chaudhari, N. Transcriptomes and neurotransmitter profiles of classes of gustatory and somatosensory neurons in the geniculate ganglion. Nat. Commun. 2017, 8, 1–16. [Google Scholar] [CrossRef]
  311. Vandenbeuch, A.; Tizzano, M.; Anderson, C.B.; Stone, L.M.; Goldberg, D.; Kinnamon, S.C. Evidence for a role of glutamate as an efferent transmitter in taste buds. BMC Neurosci. 2010, 11, 77. [Google Scholar] [CrossRef] [Green Version]
  312. Chang, R.B.; Waters, H.; Liman, E.R. A proton current drives action potentials in genetically identified sour taste cells. Proc. Natl. Acad. Sci. USA 2010, 107, 22320–22325. [Google Scholar] [CrossRef] [Green Version]
  313. Horio, N.; Yoshida, R.; Yasumatsu, K.; Yanagawa, Y.; Ishimaru, Y.; Matsunami, H.; Ninomiya, Y. Sour taste responses in mice lacking PKD channels. PLoS ONE 2011, 6, e20007. [Google Scholar] [CrossRef]
  314. La Sala, M.S.; Hurtado, M.D.; Brown, A.R.; Bohórquez, D.V.; Liddle, R.A.; Herzog, H.; Zolotukhin, S.; Dotson, C.D. Modulation of taste responsiveness by the satiation hormone peptide YY. FASEB J. 2013, 27, 5022–5033. [Google Scholar] [CrossRef] [Green Version]
  315. Ping, W.; Xu, G.; Qin, L.; Xu, Y..; Li, Y.; Li, R. Cell-based biosensors and its application in biomedicine. Sens. Actuators B Chem. 2005, 108, 576–584. [Google Scholar] [CrossRef]
  316. Ziegler, C. Cell-based biosensors. Fresenius’ J. Anal. Chem. 2000, 366, 552–559. [Google Scholar] [CrossRef] [PubMed]
  317. Gui, Q.; Lawson, T.; Shan, S.; Yan, L.; Liu, Y. The Application of Whole Cell-Based Biosensors for Use in Environmental Analysis and in Medical Diagnostics. Sensors (Basel) 2017, 17, 1623. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  318. Gupta, N.; Renugopalakrishnan, V.; Liepmann, D.; Paulmurugan, R.; Malhotra, B.D. Cell-based biosensors: Recent trends, challenges and future perspectives. Biosens. Bioelectron. 2019, 141, 111435. [Google Scholar] [CrossRef] [PubMed]
  319. Berg, K.A.; Clarke, W.P.; Sailstad, C.; Saltzman, A.; Maayani, S. Signal transduction differences between 5-hydroxytryptamine type 2A and type 2C receptor systems. Mol. Pharmacol. 1994, 46, 477–484. [Google Scholar] [PubMed]
  320. Akiyoshi, J.; Isogawa, K.; Yamada, K.; Nagayama, H.; Fujii, I. Effects of antidepressants on intracellular Ca2+ mobilization in CHO cells transfected with the human 5-HT2C receptors. Biol. Psychiatry 1996, 39, 1000–1008. [Google Scholar] [CrossRef]
  321. Kawashima, E.; Estoppey, D.; Virginio, C.; Fahmi, D.; Rees, S.; Surprenant, A.; North, R.A. A novel and efficient method for the stable expression of heteromeric ion channels in mammalian cells. Recept. Channels 1998, 5, 53–60. [Google Scholar]
  322. Jiao, X.; Gonzalez-Cabrera, P.J.; Xiao, L.; Bradley, M.E.; Abel, P.W.; Jeffries, W.B. Tonic inhibitory role for cAMP in alpha(1a)-adrenergic receptor coupling to extracellular signal-regulated kinases ½. J. Pharmacol. Exp. Ther. 2002, 303, 247–256. [Google Scholar] [CrossRef]
  323. Romanov, R.A.; Rogachevskaja, O.A.; Khokhlov, A.A.; Kolesnikov, S.S. Voltage dependence of ATP secretion in mammalian taste cells. J. Gen. Physiol. 2008, 132, 731–744. [Google Scholar] [CrossRef] [Green Version]
  324. Huang, A.Y.; Wu, S.Y. Calcitonin Gene-Related Peptide Reduces Taste-Evoked ATP Secretion from Mouse Taste Buds. J. Neurosci. 2015, 35, 12714–12724. [Google Scholar] [CrossRef]
  325. Dando, R.; Dvoryanchikov, G.; Pereira, E.; Chaudhari, N.; Roper, S.D. Adenosine enhances sweet taste through A2B receptors in the taste bud. J. Neurosci. 2012, 32, 322–330. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  326. Leenders, A.G.M.; Sheng, Z.-H. Modulation of neurotransmitter release by the second messenger-activated protein kinases: Implications for presynaptic plasticity. Pharmacol. Ther. 2005, 105, 69–84. [Google Scholar] [CrossRef] [Green Version]
  327. Liu, Z.; Liu, J.; Zhang, S.; Xing, X.-H.; Su, Z. Microbial fuel cell based biosensor for in situ monitoring of anaerobic digestion process. Bioresour. Technol. 2011, 102, 10221–10229. [Google Scholar] [CrossRef] [PubMed]
  328. HUANG, Y.-J.; MARUYAMA, Y.; LU, K.-S.; PEREIRA, E.; PLONSKY, I.; BAUR, J.E.; WU, D.; Roper, S.D. USING BIOSENSORS TO DETECT THE RELEASE OF SEROTONIN FROM TASTE BUDS DURING TASTE STIMULATION. Arch. Ital. Biol. 2005, 143, 87–96. [Google Scholar] [PubMed]
  329. Huang, Y.A.; Roper, S.D. Intracellular Ca(2+) and TRPM5-mediated membrane depolarization produce ATP secretion from taste receptor cells. J. Physiol. (Lond) 2010, 588, 2343–2350. [Google Scholar] [CrossRef] [PubMed]
  330. Glendinning, J.I.; Bloom, L.D.; Onishi, M.; Zheng, K.H.; Damak, S.; Margolskee, R.F.; Spector, A.C. Contribution of α-Gustducin to Taste-guided Licking Responses of Mice. Chem Senses 2005, 30, 299–316. [Google Scholar] [CrossRef]
  331. Ruiz-Avila, L.; McLaughlin, S.K.; Wildman, D.; McKinnon, P.J.; Robichon, A.; Spickofsky, N.; Margolskee, R.F. Coupling of bitter receptor to phosphodiesterase through transducin in taste receptor cells. Nature 1995, 376, 80–85. [Google Scholar] [CrossRef]
  332. Glendinning, J.I.; Frim, Y.G.; Hochman, A.; Lubitz, G.S.; Basile, A.J.; Sclafani, A. Glucose elicits cephalic-phase insulin release in mice by activating KATP channels in taste cells. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2017, 312, R597–R610. [Google Scholar] [CrossRef] [Green Version]
  333. Dotson, C.D.; Roper, S.D.; Spector, A.C. PLCbeta2-independent behavioral avoidance of prototypical bitter-tasting ligands. Chem Senses 2005, 30, 593–600. [Google Scholar] [CrossRef] [Green Version]
  334. Deuschle, K.; Okumoto, S.; Fehr, M.; Looger, L.L.; Kozhukh, L.; Frommer, W.B. Construction and optimization of a family of genetically encoded metabolite sensors by semirational protein engineering. Protein Sci. 2005, 14, 2304–2314. [Google Scholar] [CrossRef]
  335. Filadi, R.; Pozzan, T. Generation and functions of second messengers microdomains. Cell Calcium 2015, 58, 405–414. [Google Scholar] [CrossRef] [PubMed]
  336. Mehta, S.; Zhang, J. Dynamic visualization of calcium-dependent signaling in cellular microdomains. Cell Calcium 2015, 58, 333–341. [Google Scholar] [CrossRef] [Green Version]
  337. Lee, J.S.; Cho, A.-N.; Jin, Y.; Kim, J.; Kim, S.; Cho, S.-W. Bio-artificial tongue with tongue extracellular matrix and primary taste cells. Biomaterials 2018, 151, 24–37. [Google Scholar] [CrossRef]
  338. Chessel, A.; Carazo Salas, R.E. From observing to predicting single-cell structure and function with high-throughput/high-content microscopy. Essays Biochem. 2019, 63, 197–208. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  339. Booij, T.H.; Price, L.S.; Danen, E.H.J. 3D Cell-Based Assays for Drug Screens: Challenges in Imaging, Image Analysis, and High-Content Analysis. SLAS Discov. 2019, 24, 615–627. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  340. Nürnberg, E.; Vitacolonna, M.; Klicks, J.; Von Molitor, E.; Cesetti, T.; Keller, F.; Bruch, R.; Ertongur-Fauth, T.; Riedel, K.; Scholzt, P.; et al. Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward. Front. Mol. Biosci. 2020, 7, 20. [Google Scholar] [CrossRef] [PubMed]
  341. Li, T.; Lu, G.; Chiang, E.Y.; Chernov-Rogan, T.; Grogan, J.L.; Chen, J. High-throughput electrophysiological assays for voltage gated ion channels using SyncroPatch 768PE. PLoS ONE 2017, 12, e0180154. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Schematic overview of cells, tissues and organs involved in taste perception. In the periphery, primary taste transduction uses different receptors and intra- and intercellular pathways (indicated) that occur in taste cells of type I–III (upper right). These are organized in taste buds (upper left), which are organized in circumvallate, foliate or fungiform papillae (center) of the tongue (lower left). From there, sensory information is passed on by glossopharyngeal, chorda tympani and vagus nerves (lower right) to the brain (right). Here, signals first arrive at the nucleus of the solitary tract in the brain stem, from where they get relayed to the thalamus and then to the gustatory cortex for final processing.
Figure 1. Schematic overview of cells, tissues and organs involved in taste perception. In the periphery, primary taste transduction uses different receptors and intra- and intercellular pathways (indicated) that occur in taste cells of type I–III (upper right). These are organized in taste buds (upper left), which are organized in circumvallate, foliate or fungiform papillae (center) of the tongue (lower left). From there, sensory information is passed on by glossopharyngeal, chorda tympani and vagus nerves (lower right) to the brain (right). Here, signals first arrive at the nucleus of the solitary tract in the brain stem, from where they get relayed to the thalamus and then to the gustatory cortex for final processing.
Sensors 20 01811 g001
Figure 2. Taste transduction of the five basic taste modalities. Schematic overview of the currently known principal signaling pathways involved in primary taste transduction occurring in taste cells (type as indicated) and their output to neighboring taste cells or gustatory nerve fibers (lower part). The use of molecular fluorescent biosensors for specific research questions, as described in the main text, is indicated here by yellow boxes. For detailed descriptions of signaling pathways and the use of biosensors, please refer to the main text. Elusive aspects are indicated by question marks. Abbreviations of signaling molecules: 5HT: serotonin, AC: adenylate cyclase, CALHM: calcium homeostasis modulator channel, ENaC: epithelial sodium channel, IP3: inositol-3-phophate, IP3R: inositol-3-phosphate receptor, Kir2.1: inward-rectifier potassium ion channel 2.1, P2X/P2Y: purinergic receptors, PDE: phosphodiesterase, PKA: protein kinase A, PKD1L: polycystic-kidney-disease-like ion channel; PLC: phospholipase C, TRPM5: receptor potential M5 channel, V1R: vanilloid receptor 1, VGCC: voltage-gated calcium channel, VGKC: voltage-gated potassium channel, VGSC: voltage-gated sodium channel, αGus: α-subunit of the G-protein gustducin.
Figure 2. Taste transduction of the five basic taste modalities. Schematic overview of the currently known principal signaling pathways involved in primary taste transduction occurring in taste cells (type as indicated) and their output to neighboring taste cells or gustatory nerve fibers (lower part). The use of molecular fluorescent biosensors for specific research questions, as described in the main text, is indicated here by yellow boxes. For detailed descriptions of signaling pathways and the use of biosensors, please refer to the main text. Elusive aspects are indicated by question marks. Abbreviations of signaling molecules: 5HT: serotonin, AC: adenylate cyclase, CALHM: calcium homeostasis modulator channel, ENaC: epithelial sodium channel, IP3: inositol-3-phophate, IP3R: inositol-3-phosphate receptor, Kir2.1: inward-rectifier potassium ion channel 2.1, P2X/P2Y: purinergic receptors, PDE: phosphodiesterase, PKA: protein kinase A, PKD1L: polycystic-kidney-disease-like ion channel; PLC: phospholipase C, TRPM5: receptor potential M5 channel, V1R: vanilloid receptor 1, VGCC: voltage-gated calcium channel, VGKC: voltage-gated potassium channel, VGSC: voltage-gated sodium channel, αGus: α-subunit of the G-protein gustducin.
Sensors 20 01811 g002
Figure 3. Biological models taking advantage of optical biosensors to study taste signaling. Schematic overview of the four major types of test systems used so far to investigate taste perception. Frequently applied molecular optical biosensors are depicted with green letters, curly red lines indicate local application of tastants. For further details, please refer to the main text.
Figure 3. Biological models taking advantage of optical biosensors to study taste signaling. Schematic overview of the four major types of test systems used so far to investigate taste perception. Frequently applied molecular optical biosensors are depicted with green letters, curly red lines indicate local application of tastants. For further details, please refer to the main text.
Sensors 20 01811 g003
Figure 4. Use of a 3D culture with immortalized human tongue cells expressing a GECI to study Ca2+ responses upon perfusion of a bitter compound. Dynarray chips (300 Microns) were filled with 5000 HTC-8-G-GECO cells/cavity and cultured for three (AC) or seven days (D,E). (A) Bright-field image. (B) Representative confocal fluorescence image of one optical plane at 30 µm from the top of the chip. Upon fixation, cells were labelled with markers for f-actin (phalloidin, red) and nuclei (DAPI, blue). (C) Confocal micrograph showing a side view of a chip cavity. Before microscopy, the chip was PFA-fixed and sliced. (D) Representative time course of HTC-8-G-GECO fluorescence changes (ΔF/F0, normalized to the time before compound perfusion). The chip was mounted in an Ibidi perfusion slide, stabilized with gelatine pads (Scaffolene, from Freudenberg) and then perfused with salicine (20 mM) (all procedures analogous to [179]). Traces show G-GECO fluorescence changes as a function of time, the time period of salicine perfusion is indicated by a grey bar. (E) Examples of pseudo-colored confocal images during perfusion in control (left panel) and in salicine solutions (middle and right panels). Blue and yellow/red cues indicate low and high G-GECO fluorescence intensities, respectively. Time points of image acquisition correspond to graph in (D). Images were acquired with an inverted Leica TCS SP8 confocal microscope. Scale bars in (A–C) and (E), 100 µm. (Unpublished data E.M. and T.C.)
Figure 4. Use of a 3D culture with immortalized human tongue cells expressing a GECI to study Ca2+ responses upon perfusion of a bitter compound. Dynarray chips (300 Microns) were filled with 5000 HTC-8-G-GECO cells/cavity and cultured for three (AC) or seven days (D,E). (A) Bright-field image. (B) Representative confocal fluorescence image of one optical plane at 30 µm from the top of the chip. Upon fixation, cells were labelled with markers for f-actin (phalloidin, red) and nuclei (DAPI, blue). (C) Confocal micrograph showing a side view of a chip cavity. Before microscopy, the chip was PFA-fixed and sliced. (D) Representative time course of HTC-8-G-GECO fluorescence changes (ΔF/F0, normalized to the time before compound perfusion). The chip was mounted in an Ibidi perfusion slide, stabilized with gelatine pads (Scaffolene, from Freudenberg) and then perfused with salicine (20 mM) (all procedures analogous to [179]). Traces show G-GECO fluorescence changes as a function of time, the time period of salicine perfusion is indicated by a grey bar. (E) Examples of pseudo-colored confocal images during perfusion in control (left panel) and in salicine solutions (middle and right panels). Blue and yellow/red cues indicate low and high G-GECO fluorescence intensities, respectively. Time points of image acquisition correspond to graph in (D). Images were acquired with an inverted Leica TCS SP8 confocal microscope. Scale bars in (A–C) and (E), 100 µm. (Unpublished data E.M. and T.C.)
Sensors 20 01811 g004
Table 1. Fluorescent metal ion dyes used in taste research. Different indicator dyes have been used to study taste signaling in tissue/cell preparations. The readout was based on different microscopy techniques.
Table 1. Fluorescent metal ion dyes used in taste research. Different indicator dyes have been used to study taste signaling in tissue/cell preparations. The readout was based on different microscopy techniques.
Cell/TissueSpeciesImagingSensorDetectStimuliMicroscopy TechniqueSource
Dissociated taste cellsHamsterEx vivoBCECF-AMpHSourConventional[164]
Single fungiform papillaRat[66]
SlicesMouseBCECF-D/AM
+ CaO
+ lucifer yellow
Ca2+, pH Confocal[59]
EpitheliumMouseCaGD Ca2+Salt[46,48]
Dissociated cells, slicesMouseSour, kokumi bitter, umami, K+[56,100,114,159]
SlicesRatSweet umami bitter, salt, sour[74,157,161,165]
Isolated taste budsRatCaG-AMSourConventional[166]
Isolated taste buds, slicesMouse
PLCβ2-GFP
Fura-2
CaGD/CaOD
Adenosine[42]
Dissociated cells, isolated taste buds, slicesMouseGABAConfocal[41]
Dissociated cellsMouse
GAD-GFP
Fura-2 SourNot stated[150]
Dissociated cells, isolated taste budsMouseATPConventional[140,144,167]
Dissociated cells, cell aggregatesRatBitter[50,103,133,141]
Dissociated cellsMouseBitter, umami, sweet,
ryanodine
Confocal[37,168,169,170]
Dissociated cells, isolated taste budsMouse
PLCβ2-GFP
Glutamate[143]
Dissociated cellsMouse GAD67-GFPIBMX, ForskolinConventional [149]
Dissociated cellsMouse
T1R3-GFP/TRPM5-GFP
K+[113]
Dissociated cellsMouseBitter,
adrenergic agonist, K+
[147]
Dissociated cells, isolated taste budsMouseOxytocineNot stated[142]
Dissociated cells, isolated taste budsRatSweet, ForskolinConventional [139]
Dissociated cellsMouse/MudpuppyBitter[171]
Dissociated cellsMouse/HumanFatty acid[98]
FACS isolated CD36 pos. cellsMousePrimary
culture
Fura-2-AM Fatty acid,Confocal[97]
Primary culture of taste cellsHumanSweet, bitterPlate reader[125]
Dissociated cellsMouseEx vivoFura-2
AsanteNaTrump-2
Ca2+,
Na+
Bitter, sweet, umamiConfocal [151]
SlicesMouseGCaMP3 in type II and III cellsCa2+Salt +
AF-568,647 or fluorescein
[55]
TongueMouseIn vivoCaGDSweet, salt, sour, bitterTwo-photon[77]
3D culture (organoids)Mouse2D cell cultureFura-2Sweet, salt, sour, bitterConventional[127]
Isolated taste budChickenEx vivo Fluo-4-AMBitter, umamiConfocal[172]
Dissociated cells, isolated taste budsMouseFluo-4M
Np-EGTA-AM
Ca2++ uncagingATPConventional [156]
Table 2. Biosensors used to study taste in the brain. Taste bud are innervated by sensory neurons that convey the information to the CNS. This has been studied with live imaging microscopy in vivo with mostly genetically encoded Ca2+ sensors. Abbreviations: NTS: solitary tract, PBN: parabranchial nucleus, GC: gustatory cortex, genic.gangl: geniculate ganglion, Tr.: transgenic.
Table 2. Biosensors used to study taste in the brain. Taste bud are innervated by sensory neurons that convey the information to the CNS. This has been studied with live imaging microscopy in vivo with mostly genetically encoded Ca2+ sensors. Abbreviations: NTS: solitary tract, PBN: parabranchial nucleus, GC: gustatory cortex, genic.gangl: geniculate ganglion, Tr.: transgenic.
RegionSpeciesTransgenic ModelTracingSensorDetectStimuliMicroscopy TechniqueSource
Genic.gangl.Mouse Tr. mouse
5HT3A-GFP
Fura-2/Fluoro-GoldCa2+5HTConfocal [38]
Tr. mouse
Pirt-GCamMP3
GCaMP3Sweet, bitter, umami, salt, sour[205]
Tr. mouse
Thy1-GCaMP3
AVV-GCaMP3
(retrograde/NTS)
Two-photon[201]
NTSTr. mouse
T2R5,
tWGA-DsRed
Zif268Sweet, bitterConventional[206]
PBNMouse
SatB2-Cre
Vglut2-ihres-Cre
AAV1-Cre-GCaMP6sAAV8-Cre-synaptophysin-mCherry
AAV5-DIO-ChR2-EYFPin PBN
GCaMP6sCa2+
c-fos
BitterMiniaturized[208]
Brain stemZebra fishTr. fish
Elav3-GCaMP5
GCaMP5Ca2+Sweet, bitter, umami, sourTwo-photon[213]
GC MouseAVV1-GCaMP6sAVV1-mCherry/microruby dextran
(anterograde-thalamus)
GCaMP6sSweet, bitter, salt, sour[192]
AAV2/1-GCaMP6sCAV2-Cre in hCAR x dTomato mice
(retrograde-amygdala)
Bitter[207]
Mouse
T2R5/T1R2 knockout
AVV2-GFP
(anterograde-thalamus)
GCaMP6s
OGB-AM + sulforhodamine 101
Sweet, bitter, umami, salt[202]
Table 3. Overview of recombinant systems that were used to study taste receptor function and new agonists/antagonists. Listed are different stimuli, which were investigated with Ca2+ sensors in host cells expressing recombinant proteins of the taste signaling machinery.
Table 3. Overview of recombinant systems that were used to study taste receptor function and new agonists/antagonists. Listed are different stimuli, which were investigated with Ca2+ sensors in host cells expressing recombinant proteins of the taste signaling machinery.
Host CellStimuliCa2+ SensorReadoutIntroduced GenesSource
HEK293BitterFura-2MicroscopyGα15+T2R3-5-10-16[47]
Fura-AMGα16gust44/ Gα16gust37+T2R5-16[259]
Plate readerGα16gust44+T2R46[288]
Gα16gust44+T2R46-43-31[265]
Fluo-AMGα16gust44+T2R14[289]
Gα16gust44+variants of T2R16 [276]
Gα16gust44+T2R43-44-4-46-50[290]
Gα16gust44+T2R31[279]
Gα16gust44+T2R16[291]
Gα16gust44+T2R43-44[72]
Gα15T2R16[292]
Fluo-4Gα16gust44+hT2R31[279]
Gα16gust44+T2Rs (25 different types)[73]
SweetFura-AMV1R[261]
Fluo-AMGα15+T1R2+T1R3[293]
Gα16gust44+fT1R2+T1R3[266,271]
Fura-2Gα16gust44+T1R2/R3 or T2R44[294]
Microscopy Gα15+T1R2+T1R3[83]
Sweet, umamiFluo-AMGα15+T1R2+T1R3
Gα15+T1R1+T1R3
[93]
AcidFura-2-AMPKD1L3+PKD2L1[260]
[264]
Fura-2[150]
Fluo-AM[154]
KokumiFluo-8, Flamindo (for cAMP)CaSR[263]
Table 4. Overview of reporter genes used to study taste signaling in specific cell populations. Different reporter genes were expressed under the control of diverse promoters of genes involved in the taste signaling cascade.
Table 4. Overview of reporter genes used to study taste signaling in specific cell populations. Different reporter genes were expressed under the control of diverse promoters of genes involved in the taste signaling cascade.
PromoterReporter GeneSensorReadoutStimuliSource
GustducinlacZ
β–galactosidase
No Ca2+ imagingCa2+MicroscopyBitter[111]
GFPNo Ca2+ imaging[79]
Fura-2[141]
PLCβ2CaOD[297]
KCl[49]
PLCβ2, GADSweet, bitter, umami, sour, salt[114]
Sweet, bitter, umami[33]
Sweet, bitter, umami, ACh[42]
PLCβ2, GAD
OXTR
Fura-2-AM Oxytocin[142]
T1R3
GAD
Glutamate[311]
IP3RBitter, KCl[50]
TRPM5
T1R3
Fura-2-AMKCl[113]
TRPM5CFPFluo-5FCa2+[112]
T2R32GFP SapphireCaGDKCl[46]
PKD2L1YFPCarboxi-DFFDA + H+ uncagingpHSour [312]
Fura-2-AM
pHrodo-Red-AM
pH, Ca2+[69]
GADGFPNo Ca2+ imagingCa2+[67]
[313]
Fura-2[150]
IBMX-forskolin[149]
PYYNo Ca2+ imagingBitter, lipids, sour, sweet, bitter, umami, salt[314]
Table 5. Biosensor cells that can be used to study neurotransmitter release from taste cells. Upon sensing neurotransmitters, BC evoke intracellular Ca2+ transients that can be detected with Ca2+-sensor dyes. Abbreviations: 5HT: serotonin, NA: noradrenaline, Ach: achetylcholine.
Table 5. Biosensor cells that can be used to study neurotransmitter release from taste cells. Upon sensing neurotransmitters, BC evoke intracellular Ca2+ transients that can be detected with Ca2+-sensor dyes. Abbreviations: 5HT: serotonin, NA: noradrenaline, Ach: achetylcholine.
BCCa2+ SensorReadoutStimuliReceptor NeurotransmitterSource
CHOFura-2-AMMicroscopyKCl, sour, sweet, bitter, ATP5HT2c5HT[36,328]
5HT2c or
P2X2/P2X3
5HT
ATP
[37,41,56,105,143]
Adenosine[325]
Calcitonin gene-related peptideNA
5-HT
[324]
KCl, sour, sweet, bitter5HT2c
or α1A or dual
NA
5HT
[39]
Sweet, bitter, KClP2X2/P2X3ATP[329]
KCl, sour, sweet, bitterGABAB+ Gαqo5GABA[40]
Sweet, umami, bitter
(fluorescein)
M3r
P2X2/P2X3
ACh
ATP
[42]
KCl, taste mix, substance PP GABAB+ Gαqo5 or 2X2/P2X3GABA, ATP[104]
COS-1Fluo-4Bitter, sour, depolarization, ACh, 5HT, NA, glutamateP2Y endogenousATP
ACh
[32,323]

Share and Cite

MDPI and ACS Style

von Molitor, E.; Riedel, K.; Hafner, M.; Rudolf, R.; Cesetti, T. Sensing Senses: Optical Biosensors to Study Gustation. Sensors 2020, 20, 1811. https://doi.org/10.3390/s20071811

AMA Style

von Molitor E, Riedel K, Hafner M, Rudolf R, Cesetti T. Sensing Senses: Optical Biosensors to Study Gustation. Sensors. 2020; 20(7):1811. https://doi.org/10.3390/s20071811

Chicago/Turabian Style

von Molitor, Elena, Katja Riedel, Mathias Hafner, Rüdiger Rudolf, and Tiziana Cesetti. 2020. "Sensing Senses: Optical Biosensors to Study Gustation" Sensors 20, no. 7: 1811. https://doi.org/10.3390/s20071811

APA Style

von Molitor, E., Riedel, K., Hafner, M., Rudolf, R., & Cesetti, T. (2020). Sensing Senses: Optical Biosensors to Study Gustation. Sensors, 20(7), 1811. https://doi.org/10.3390/s20071811

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop