Next Article in Journal
Protein Arginine Methyltransferases in Neuromuscular Function and Diseases
Previous Article in Journal
BMP9 Promotes an Epithelial Phenotype and a Hepatocyte-like Gene Expression Profile in Adult Hepatic Progenitor Cells
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Cells
Volume 11
Issue 3
10.3390/cells11030366
cells-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Role of the Lysosomal Cl−/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration

by
Giovanni Zifarelli
†
Institute of Biophysics—CNR, 16149 Genova, Italy
†
Current address: Centogene GmbH, 18055 Rostock, Germany.
Cells 2022, 11(3), 366; https://doi.org/10.3390/cells11030366
Submission received: 1 December 2021 / Revised: 16 January 2022 / Accepted: 19 January 2022 / Published: 21 January 2022
(This article belongs to the Section Intracellular and Plasma Membranes)
Browse Figures
Versions Notes

Abstract

CLC proteins comprise Cl− channels and anion/H+ antiporters involved in several fundamental physiological processes. ClC-7 is a lysosomal Cl−/H+ antiporter that together with its beta subunit Ostm1 has a critical role in the ionic homeostasis of lysosomes and of the osteoclasts’ resorption lacuna, although the specific underlying mechanism has so far remained elusive. Mutations in ClC-7 cause osteopetrosis, but also a form of lysosomal storage disease and neurodegeneration. Interestingly, both loss-of- and gain-of-function mutations of ClC-7 can be pathogenic, but the mechanistic implications of this finding are still unclear. This review will focus on the recent advances in our understanding of the biophysical properties of ClC-7 and of its role in human diseases with a focus on osteopetrosis and neurodegeneration.

1. Introduction

Human CLC proteins comprise Cl− channels and Cl−/H+ antiporters with fundamental roles in regulating electrical excitability, transepithelial transport and vesicular ionic homeostasis [1,2]. The lysosomal Cl−/H+ antiporter ClC-7, together with ClC-6, forms a distinct branch of the CLC protein family that is more closely related to the plant homologue AtClC-d than to the other mammalian transporters [3,4]. However, the general structural architecture of ClC-7 is very similar to the ones of the other CLC proteins with an almost identical transmembrane domain and a large cytoplasmic C-terminus comprising two CBS (cystathionine β synthase) domains [5,6] (Figure 1). ClC-7 is ubiquitously expressed with particularly high levels in the central and peripheral nervous system where it colocalizes with Lamp-1, a marker for late endosomes and lysosomes [3,7,8]. Importantly, unlike the other mammalian CLC transporters, ClC-7 requires the β subunit Ostm1 for proper localization and function [9,10,11]. In osteoclasts, ClC-7 is also expressed in the ruffled border, a specialized membrane domain responsible for the acidification of the resorption lacuna, which in turn mediates bone resorption [7]. In lysosomes and in the ruffled border, ClC-7 contributes to the ionic homeostasis, even though the specific role is still debated [9,12,13,14]. Mutations in ClC-7 and Ostm1 cause osteopetrosis [7,9,10], but also a form of lysosomal storage disease and neurodegeneration [8,15,16], consistent with the phenotype of ClC-7 and Ostm1 loss-of-function mouse models [7,10]. ClC-7 expression has also been detected in the luminal membrane of the choroid plexus [17], but its physiological role in that context is still unclear. Intriguingly, CLCN7 has been identified as the causative gene in a quite unique phenotype combining osteopetrosis, renal tubule acidosis, renal stones, epilepsy, and blindness [18]. Moreover, ClC-7 has been implicated in Alzheimer disease [19]. Interestingly, both loss-of- and gain-of-function mutations of ClC-7 can be pathogenic, although the mechanistic implications of these findings are still unclear. This review will focus on the recent advances in our understanding of the biophysical properties of ClC-7 and of its role in human physiology (in particular in osteopetrosis and neurodegeneration) and will try to provide an integrated perspective from these two fields of investigation.

2. The Structure of ClC-7

Two recent cryo-EM studies have elucidated the structure of the ClC-7/Ostm1 complex [5,6]. The association between the two proteins is largely based on interactions of their transmembrane regions at the periphery of the ClC-7 dimer [5,6] (Figure 1). Importantly, the highly glycosylated luminal region of Ostm1 forms a bundle that covers the luminal side of ClC-7, explaining the protective role of Ostm1 against the degradative environment of the lysosomal lumen [5,6]. In other respects, the structure of ClC-7 reproduces most of the key features of the other CLC proteins of known structure [20,21,22,23,24,25]: a dimeric architecture with a transmembrane domain and a large cytosolic region comprising two CBS domains. The ion permeation pathway present in each of the monomers is also very conserved, with a typical “hourglass” shape with a narrowing at the selectivity filter and three anion binding sites (Figure 1).
In particular, in the study of Schrecker et al., a conserved glutamate residue (Glu247 in the hClC-7) with an important role in voltage dependence and Cl−/H+ coupling in all CLC transporters (so-called “gating glutamate”) is captured with the side chain directed towards the extracellular space and Cl− ions occupying all three binding sites [6] (Figure 1). The structure of the hClC-7 was also investigated by Zhang et al., but they did not identify densities for Cl− ions and could not build an unbiased model for the side chain of the gating glutamate [5]. The pathway for proton movement appears to bifurcate from the Cl− passageway close to the central binding site and be formed by a putatively water-filled cavity around another glutamate residue that is very conserved in mammalian CLC transporters (Glu314 in the hClC-7, so called “proton glutamate”) [5,6], consistent with previous structures and molecular dynamics simulations [26,27,28]. In the cytosolic region, the structure of ClC-7 reveals a previously unrecognized role for the N-terminal domain which interacts both with the transmembrane region and the CBS1 and CBS2 domains forming an extensive intramolecular interaction network [5,6]. Intriguingly, the loop of the N-terminus responsible for this interaction is conserved, among the human CLC transporters, only in ClC-6 [6]. Importantly, the N-terminus in the structures of other CLC proteins was not resolved, probably due to the intrinsic flexibility, and it is, therefore, not possible to conclude whether this role for the N-terminus is unique to ClC-7 or it is relevant also for ClC-6 and other CLC proteins. The CBS domains, with contribution from the N-terminal domain, were found to bind an ATP molecule [6] (Figure 1). The binding coordination was similar to the one observed in the isolated C-terminal portion of ClC-5 [29], but in addition, in ClC-7, a Mg2+ ion is also present (Figure 1). Notably, Leisle et al. showed that ClC-7 currents are not affected by ATP [11]. A comparison between the structure of ClC-7 with and without Ostm1 reveals that there are no large-scale differences in the transmembrane region and in ATP and lipid binding (see also below) [6]. However, some subtle structural rearrangements are indeed observed in the permeation pathway and in the structure of the ClC-7/Ostm1 complex the anion occupancy at the central binding site is much lower than in ClC-7 alone [6].

Phosphatidylinositol Binding Site

Phosphatidylinositol-3-phosphate (PI3P) is a low-abundance constituent of lysosome membranes. Schrecker et al. were able to resolve a molecule of PI3P at the interface between the transmembrane and the cytoplasmic domains [6] (Figure 1). The transmembrane region responsible for the interaction with the phosphate head group is formed by an amphipatic β hairpin between helices αF and αG which is conserved also in ClC-6 and in the plant nitrate/H+ antiporter AtClC-a [6], but not in other mammalian CLC proteins. Given the specific lipid composition of lysosomes membranes this finding might be of great biophysical and physiological relevance, but its potential consequences remain to be investigated.

3. Cl−/H+ Exchange and Transport Mechanism in CLC Antiporters

A central aspect of CLC transporter function is the coupled movement of Cl− and H+ in opposite directions with a stoichiometry of 2 to 1 [11,12,30,31]. The Cl− and H+ pathways are schematically represented in Figure 2, indicating that they are different but intersect at the level of the gating glutamate. Importantly, CLC proteins are unique in that the two transported substrates, Cl− and H+, bind simultaneously and not sequentially as in the classical alternate access mechanism common to most transporters [32,33]. At the cytosolic side, Cl− and H+ pathways diverge as the proton glutamate that probably serves as a proton acceptor site [34,35] is displaced from the cytosolic opening of the anion permeation pathway [5,6]. Computational studies have also suggested the presence of water-filled protein cavities that might potentially bridge the proton glutamate and the gating glutamate and mediate proton transport [26,36]. At the central binding site, Cl− and H+ pathways converge as mutations of the conserved serine residue that coordinates the anion at this site affected both anion selectivity and anion/H+ coupling [31,37,38]. Regarding the Cl− and H+ pathways from the luminal space to the central binding site, it was assumed for a long time that they would superimpose. Proton would move towards the central binding site as the protonated side chain of the gating glutamate would move from the luminal space to the external and then the central binding site. In this model, proton movement down to the central binding site would result from the competition between the protonated side chain of the gating glutamate and Cl− ions for the external and central binding site [39]. However, very recently Leisle et al. proposed a different model illustrated in a simplified version in Figure 2, in which the movement of the protonated side chain of the gating glutamate does not take place along the Cl− permeation pathway, but rather in the interior of the protein with a critical contribution of two phenylalanine residues, one of which also contributes to the central anion binding site [27]. According to this model, movement of the protonated gating glutamate and the rearrangement of the phenylalanine of the central binding site are coupled to the opening of the intracellular gate formed by conserved serine and tyrosine residues below the central binding site [27].

4. Electrophysiological Properties of ClC-7

The electrophysiological investigation of ClC-7 has been possible after the discovery that disruption of N-terminal dileucine lysosomal targeting motifs by alanine substitution produced a partial redistribution of the complex ClC-7/Ostm1 to the plasma membrane [40] and this was sufficient to elicit robust transmembrane current [11,41]. Interestingly, whereas the strong outward rectification of the currents and the inhibitory effect of acidic extracellular pH are properties that ClC-7 shares with other CLC transporters [11,41], there are also important differences. In fact, ClC-7 displays a very slow activation kinetics with a time constant in the order of seconds whereas for the other CLC transporters investigated so far the activation is to a large extent instantaneous [11,41]. However, it should be kept in mind that these are properties observed upon expression of ClC-7 at the plasma membrane, and these might differ from the ones in the physiological location, the lysosomal membrane, in particular, because of the different lipid composition and the observed PI3P binding to ClC-7 [6], but also due to the potential presence of unidentified lysosomal binding proteins.

4.1. The Role of the Proton Glutamate

Another important difference is related to the function of the so-called “proton glutamate”, E312 in rClC-7. Neutralization of this conserved residue in ClC-3, ClC-4, ClC-5 and ClC-6 ablates transport activity [42,43,44]. Under the assumption that in ClC-7 neutralization of the proton glutamate would have the same effect, Weinert et al. generated a knock-in mouse model (so called transport deficient, or “td”) carrying the E312A mutation to explore possible roles of ClC-7 that were unrelated to ion-transport [45]. Indeed, the mutation resulted in an osteopetrosis that was as severe as in the ClC-7 KO mice but with milder neurodegeneration and no defect in pigmentation, suggesting that there was also a functional role for a transport-deficient ClC-7, for example, in contributing to the assembly of a lysosomal macromolecular complex [45]. Leisle et al. later suggested that indeed the E312A mutation ablates transport current in ClC-7 [11]. However, a detailed electrophysiological characterization recently showed that this mutant does mediate transport currents, although their magnitude is strongly reduced compared to WT [41]. This finding potentially explains the phenotype of the E312A knock-in mouse model, as the residual current mediated by the E312A mutant could rescue the pigmentation phenotype and ameliorate the neurodegeneration compared to a full ClC-7 KO. However, further studies are required to fully clarify this point.

4.2. Transient Capacitive Currents

The work of Pusch et al. also suggested another specific feature of ClC-7 related to the mechanism that originates the transient capacitive currents [41]. Proton glutamate neutralizing mutations in ClC-3, ClC-4 and ClC-5 not only ablate transport current, but are also associated with either the appearance or an increase in magnitude of transient capacitive currents [44,46,47,48,49]. A detailed analysis of transport current in ClC-5 suggested that the protein switches between transport-incompetent (or “inactive) and transport-competent (or “active”) states [42,48], leading to the proposal that the transient capacitive currents observed in the proton glutamate mutations would reflect charge movement associated with gating transitions (transition between inactive and active state) rather than transport activity. For ClC-7, the situation appears very different. First of all, the activation kinetics of transport currents in ClC-7 is order of magnitude slower than in ClC-5 (seconds vs. milliseconds) [11,41]. Moreover, in ClC-7, the transient current appears to be linked to the transport cycle itself rather than to a gating process that precedes transport since the transient current amplitude is independent of the fraction of activated transporters and it is the same in the WT and in the mutant R760Q although the activation kinetics of the mutant is much faster [11,41].

5. Osteopetrosis

Physiological bone tissue remodeling requires a balance between bone formation and resorption mediated by osteoblasts and osteoclasts, respectively. In osteopetrosis this balance is disturbed as bone resorption is impaired resulting in dense but fragile bones [50]. The molecular mechanism of bone resorption by osteoclasts is based on a specialized domain, the ruffled border, formed in the area where the osteoclasts tightly seal on the bone matrix. Protons and secretory lysosomes containing bone-resorbing enzymes are released into the ruffled border to attack both the inorganic and organic matrix of bones [51]. In particular, osteoclast-rich osteopetrosis indicates a form of osteopetrosis in which the number of osteoclasts is not reduced, and osteoclasts actually have a higher survival rate and increased surface area, most probably due to the reduced release of proapoptotic signals during bone resorption [51]. Osteoclast-poor osteopetrosis indicates an osteopetrosis caused by a reduced number of osteoclasts and with a milder phenotype compared to the osteoclast-rich form. Classically, two main forms of osteoclast-rich osteopetrosis can be distinguished, depending on the inheritance pattern: autosomal dominant osteopetrosis (ADO, or OPTA) and autosomal recessive (ARO, or OPTB). However, they are both heterogeneous from the genetic, mechanistic, and phenotypic point of view, and correspondingly they comprise a broad spectrum of clinical manifestations [52,53]. Here, we will discuss in more detail the forms of osteopetrosis caused by mutations in ClC-7 (Figure 3 and Table 1).

5.1. Autosomal Dominant Osteopetrosis Type II (ADO II)

Regarding the types of osteopetrosis due to ClC-7 dysfunction, ADO type II (also OPTA2 or Albers-Schonberg disease type II) is the most common form with a prevalence of 0.2 to 5.5 in 100.000 [54]. It is usually diagnosed in late childhood/adolescence, and typical symptoms include non-traumatic fractures and skeletal-related events such as nerve compression syndrome (leading to partial visual loss) and bone marrow failure, but only rarely the is disease life-threatening [55,56]. In radiographies, it appears as segmentary osteosclerosis, predominantly at the vertebral endplates (‘rugger-jersey spine’), iliac wings (‘bone within bone’ sign), and skull base [54,56]. The disease is associated in 70% of the patients with heterozygous missense mutations in ClC-7, whereas for the remaining 30% there is no clear genetic association [57]. While ADO II is considered largely a bone disease, both old and new evidence indicates very important extra-skeletal manifestations, a fact which is actually consistent with the broad ClC-7 tissue distribution [3,15,58]. One indication of such extra-skeletal manifestations is the long-known increase in creatine kinase observed in several osteopetrosis patients, which suggests a myopathy phenotype [59]. Interestingly, a detailed investigation of heterozygous G213R mice, representing a validated model of human ADO II, revealed that they also have several extra-skeletal manifestations, showing anxiety, depression, β-amyloid accumulation, and astrogliosis, suggesting a relevant involvement of the nervous system [57]. In addition, lung, kidney, spleen and muscle are also affected through macrophage infiltration and activation of fibrotic signaling [57]. Confirming these conclusions, an siRNA approach against the mutated ClC-7 was effective in improving the extra-skeletal phenotypes [57]. It is intriguing to correlate this conclusion with the findings of Rossler et al. about an ARO patient, compound heterozygous for the mutations G292E and R403Q, who presented brain abnormalities disproportionally severe in comparison to the osteosclerosis [60] (see also below). This patient died at the age of 14 months of respiratory failure. Analysis of patient hiPSCs from blood cells showed several interesting findings. In particular, an increase in the autophagy marker LC3-II in undifferentiated hiPSCs, which was also present in tissue-specific Clcn7 KO mice [15]. Defective autophagy is indeed emerging as an underlying mechanism in several neurodevelopmental disorders [61,62], and it was also observed in the mouse model carrying the heterozygous Clcn7G213R mutation (homologue of the human, G215 mutation causing ADOII) [57]. Moreover, the differentiated patient osteoclasts had a larger diameter and a higher number of nuclei compared to osteoclasts differentiated from controls, a finding already observed in both Ostm1 and ClC-7 deficient mice but still not fully understood [63,64]. The differentiated osteoclasts also showed a complete loss of bone resorption activity and upon heterologous expression and electrophysiological measurements the mutations showed an abolished (G292E) and strongly reduced (R403Q) ionic current, consistent with a fundamental loss of function as the basis of the disease [60].

5.2. Autosomal Recessive Osteopetrosis (ARO)

ARO (or OPTB4) has a prevalence of 1:250,000 in the general population, but it is much more frequent in some ethnic groups (for example in Costa Rica and northern Sweden) [65]. ARO patients have a generalized increase in bone density leading to macrocephaly, growth retardation, eye protrusion (exophthalmos), small jaw (micrognathia) and hypertelorism (increased distance between the eyes). The most severe forms of ARO are often neuropathic due to primary neurodegeneration with symptoms ranging from developmental delay to hypotonia, retinal atrophy and seizures [50,66]. Other symptoms are due to the constriction of bone marrow space like anemia, thrombocytopaenia, compensatory extramedullary hematopoiesis, hepatosplenomegaly, and recurrent infections [67]. ARO is also often associated with low serum Ca2+ and secondary hyperparathyroidism [68]. It is usually diagnosed at birth or early infancy, and it is often lethal in early life if not treated with hematopoietic stem cell transplantation (HSCT), but this holds only if the therapy is initiated before CNS involvement [68,69]. It is estimated that ClC-7 is responsible for 10–15% of ARO cases [52].

6. The Physiological Role of ClC-7 and Ostm1

The first indication of a role of ClC-7 in osteopetrosis came from the phenotype of ClC-7 knockout mice which recapitulated the human disease: Clcn7−/− mice showed severe osteopetrosis and retinal degeneration [7]. In particular, KO mice were smaller, had dysmorphic heads, abnormal body posture and short limbs. Excessive bone density was particularly evident in long bones which lacked a bone marrow cavity and in the failure of teeth to erupt. The survival was also affected and limited to 6–7 weeks.
As commonly observed in patients, the decrease in bone marrow caused hepatosplenomegaly secondary to extramedullary blood production also in KO mice. Retinal degeneration is often associated with osteopetrosis and was recapitulated also in KO mice. Further analysis revealed that osteoclasts were present, but developed only rudimentary ruffled borders and were unable to resorb bone in vitro because of the inability to acidify extracellular compartments [7]. The causative role of ClC-7 in human osteopetrosis was confirmed in the same study by the identification of a patient affected by ARO who was compound heterozygous for the nonsense mutations Q555x and the R762Q substitution in ClC-7 [7]. A similar mechanism is the basis for the ARO phenotype showed by the grey-lethal mouse line, harboring an inactivating mutation of Ostm1 [10]. Besides osteopetrosis, ClC-7 and Ostm1 deficient mice also have a pigmentation phenotype, which also indicates an additional physiological role [7,10]. As mentioned above, mutations in ClC-7 and Ostm1 can cause both ADO or ARO [7,10], both characterized by a spectrum of phenotypic presentation that makes the classification quite difficult when no detailed genetic data are available for the affected families [52]. In fact, there are patients that escape this schematic classification, and several ADO II mutations are present in families in which some of the carriers remain asymptomatic for the entire life whereas others develop osteopetrosis of varying degrees of severity [52,54,70,71,72,73,74]. The intermediate recessive form of the disease (IARO) described by some authors does not have a clear-cut classification, and even the mode of inheritance is questioned [52,54,74,75]. So far, only five patients have been identified with this subtype, three with the homozygous mutations G203D and P470Q [76], and P470L [77], and the two compound heterozygous L224R-K691fs [71] and V418M-R674Q [70]. In these patients, IARO is characterized by a relatively mild generalized increase in bone density with spontaneous fractures in the first years of life, mandibular prognathism, osteomyelitis, anemia, hepatosplenomegaly, and occasional optical nerve compression, but have a longer life expectancy compared to ARO [71,76]. ARO patients with mutations in either ClC-7 or Ostm1 might develop the neuropathic subtype of the disease associated with a particularly poor prognosis. Interestingly, the G215R heterozygous mutation in ClC-7 has been found in a family showing ADO II of variable expressivity and an unusual syndrome comprising renal tubular acidosis, renal stones, developmental delay, blindness, and epilepsy [18]. Intriguingly, the G215R mutation has been previously identified in several families with classical ADO II, supporting the notion of poor genotype–phenotype correlation for some ClC-7 mutations causing osteopetrosis [52,54,74].

ClC-7 Molecular Role from Animal and Cellular Models

It has been speculated for a long time that vesicular CLC proteins were chloride ion channels needed to balance positive charge accumulation produced by active proton transport into the organellar lumen, allowing for effective acidification of these compartments (reviewed in [14]). The discovery that ClC-7 is a Cl−/H+ antiporter suggested a more complex physiological role which is still debated [11,12] (Figure 4). Osteoclasts of ClC-7 KO mice failed to acidify the resorption lacuna [7] even though lysosomal pH in neurons and other cell types in ClC-7 and Ostm1 deficient mice was normal [8]. A mouse line homozygous for the uncoupling mutation E245A, so-called ClC-7unc/unc, which turns ClC-7 into a pure Cl− conductance (i.e., transforms ClC-7 from a Cl−/H+ antiporter to a Cl− channel), made it possible to investigate the specific role of Cl− transport in the regulation of lysosomal pH [13]. In comparison to ClC-7 KO mice, these mice presented a milder osteopetrosis but a similar lysosomal storage disease and no change in fur color [13].
In particular, lysosomal pH was normal, as in ClC-7 KO, but luminal [Cl−] was reduced. This suggests a specific physiological role for Cl−/H+ exchange activity in lysosomes. In contrast to this, a role for ClC-7 as shunt conductance enabling lysosomal acidification by the V-type ATPase is suggested by the impaired lysosomal acidification in cells in which ClC-7 was knocked down by siRNA [12], and by the observation that the Y715C gain of function mutation led to lysosomal hyper-acidification [78]. As explained in paragraph 4.1, in the E312A homozygous knock in mouse line (which probably has a reduced level of transport current) osteopetrosis is as severe as in ClC-7 KO mice, but neurodegeneration is milder and there is no pigmentation phenotype [45]. As for ClC-7 KO and for the ClC-7unc/unc, also the E312A homozygous mice had lysosomes with normal pH but reduced luminal [Cl−] [45]. These findings highlight the physiological importance of the lysosomal [Cl−], but also underscore the fact that general ion homeostasis (including also protons, potassium, calcium and sodium ions) in this compartment is determined by the complex interplay between ClC-7-mediated transport and several types of cation ion channels that have been newly identified at an ever-increasing pace in the last decade [79,80] (Figure 4). For example, the voltage across the lysosomal lumen is contributed by all the types of ion channels and transporters expressed in lysosomes, but in turn will also influence their activity, particularly in the case of voltage-dependent proteins [81,82]. A critical role for cation conductances in determining lysosomal pH had originally been suggested on the basis of anion substitution experiment in the seminal work of Steinberg et al. [83], and in two early pioneering works [84,85]. An increasing level of complexity with the interplay of multiple ion channels and transporters has also been suggested in a model of osteoclast resorption lacuna acidification [86].
Two mouse models of ADOII have been generated with the human mutations G215R (G213R in mouse) [87] and F316L [88]. Considering the phenotypic variability and the incomplete penetrance of human ADOII, estimated to be around 66% [89] it is interesting to note that the work of Alam et al. suggested an effect of the genetic background on the severity of the osteopetrosis symptoms of the G213R heterozygous mice [87] further supporting a role of genetic modifiers in determining the severity of the disease.
Besides KO and KI mouse lines, human induced pluripotent stem cells (hiPSCs) are also a valuable model for human diseases, and important developments have been achieved in the optimization of the differentiation protocol and functional characterization of ARO patient-derived osteoclasts [60].

7. Lysosomal Storage Disease and Neurodegeneration

Severe ARO cases are often associated with neurodegeneration manifesting in developmental delay, hypotonia, retinal atrophy and seizures [66,90,91] consistent with the finding that ClC-7 KO mice displayed neurodegeneration, with the highest impact in the hippocampus, the cortex, and the cerebellum [8]. In addition, these KO mice displayed hallmarks of neuronal ceroid lipofuscinoses (NCL) a form of lysosomal storage disease. However, the lysosomal pH of ClC-7 KO cultured neurons did not differ from WT. Neurodegeneration in ClC-7 KO mice was accompanied by microglia activation and astrogliosis, a common finding in CNS pathologies. This was indicated by overexpression of genes involved in the immune response of microglia [8] similar to what was found in mouse models of mucopolysaccharidoses, a lysosomal storage disease associated with neurodegeneration [92], and in the G213R mouse model of ADO II [57]. Like in these diseases, microglia initial activation against neuronal pathology might lead to a paradoxical response with adverse effects [93]. The retinal degeneration observed in ClC-7 KO mice is probably also due to lysosomal dysfunction [8], another finding common in NCLs. Importantly, the neurological defects were not present in a different mice model for osteopetrosis with mutation in the a3 subunit of the V-type H+ pump [94,95]. Conditional ClC-7 KO mice and tissue-specific analysis directly revealed that accumulation of lysosomal storage material is intrinsic to cells lacking ClC-7, and that the massive activation of microglia and astrocytes is limited to brain regions where ClC-7 was deleted [96]. In the same study, it was shown that in these mice the lack of ClC-7 in proximal tubule cells did not affect the endocytic activity but drastically reduced (but did not abolish) proteolysis of endocytosed protein [96].
Grey-lethal (gl) mice also showed hallmarks of lysosomal dysfunction, with accumulation of sphingolipids in the brain and increase in the autophagic marker LC3-II observed also in ClC-7 KO [96,97]. The role of ClC-7 and other CLC transporters in neurodegeneration has recently been discussed in detail by Bose et al. [16]. Interestingly, the de novo ClC-7 Y715C heterozygous mutation described in two unrelated children did not cause ADO, but a pleiotropic syndrome including albinism, developmental delay, organomegaly, and lysosomal storage [78]. Functional analysis of this mutation showed a gain-of-function with much larger currents upon expression in Xenopus oocytes and a more acidic pH of the lysosomes of patient-derived fibroblasts, which were also characterized by enlarged cytoplasmic vacuoles [78]. It is instructive to compare these findings with some recent discoveries highlighting the role of ClC-6, a late endosome CLC transporters closely related to ClC-7 and with partially overlapping localization [98,99]. ClC-6 deficient mice lack an obvious phenotype beside a very mild late onset neurodegeneration [91,98]. However, the heterozygous Y533C mutation was recently found in three patients (all heterozygous) affected by variable early-onset neurodegeneration with brainstem lesions and cortical or cerebral atrophy, respectively [100]. This mutation results in a gain of function in terms of transport current producing, when expressed in heterologous systems, a vacuolation phenotype that is similar to the one observed in the Y715C in ClC-7. However, a critical difference between the two mutations is that they lead to opposite effects on the acidification of the enlarged organelle which is increased in patient derived lysosomes with the Y715C mutation in ClC-7 but decreased in lysosomes of cells transfected with the Y533C mutation in ClC-6 [78,100]. Very recently, the ClC-6 mutation E200A was identified in patients with early infantile epileptic encephalopathy West syndrome, and it has been found to impair autophagy [101] similar to the effect of ClC-7 KO [96].

8. Structure–Function Analysis of ClC-7

Several functional analyses of disease causing mutations have been conducted [7,11,78,102,103], and in combination with the very recent structures of the ClC-7/Ostm1 complex [5,6], this provides the opportunity to test if there is any correlation between alterations of ClC-7 functional properties and the phenotype of the disease. The first observation that emerges from the mapping of ARO and ADO II mutations onto the structure of ClC-7 is that there is no single hot-spot, and mutations are distributed throughout the whole protein. A general functional feature is that the mutations that cause osteopetrosis often affect the activation kinetics, most probably through an effect on the common gate. The term common gate refers to the mechanism that controls the level of transport activity of ClC-7 in a voltage- and pH-dependent manner [14,104]. The attribute common describes the fact that it simultaneously controls the activity of both monomers of the dimeric ClC-7 (reviewed in [1]). The molecular underpinning of the common gate is still unresolved but it likely involves large conformational changes [105]. In particular, for ClC-7, it has been shown that the common gate depends on the subunit interface and both the transmembrane region and the cytoplasmic domains in the two monomers [104]. The wide distribution of osteopetrosis mutations with effects on the common gate is consistent with the notion of a large conformational change. In particular, the dimer interface between the CBS2 domains is contributed by the polar amino acids S753, R756, Lys759 and Asn774 from one monomer and Ser744, Tyr746 and Asn776 from the other monomer [5], and they are either directly involved in osteopetrosis, like Ser744, Tyr746 and S753, or are very close to residues that when mutated cause osteopetrosis (see Table 1).
Additional residues involved in osteopetrosis and located at the dimer interface are in the CBS1 domains like R674Q, G677V. Other residues in the transmembrane regions close to the dimer interface are R126, P376. M332 and P582 (ARO) and W127 F318, W319 R326 and G347 (ADO II) (Figure 2). It is important to underscore that there are also some ARO, and ADO II mutations located at the periphery of the dimers, or in any case far from the dimer interface, like I261 and R403 (ARO) and R409, V418 and S473 (ADOII). Moreover, ARO and ADO II mutations do not segregate, and in a few cases, mutation of the same residue causes ARO or ADO II depending on the specific amino acid substitution (see Table 1 and Figure 2). A specific structural feature of ClC-7 is that unlike the structures of other CLC proteins, the N-terminus is resolved and contributes to the subunit interface forming a loop with polar interactions with the transmembrane domain and the CBS2 domain [5]. The residue Y99 in this region is mutated to C in patients with ADO II [74], and several mutations of this and nearby residues produce a marked acceleration of the gating kinetics [5]. Moreover, several osteopetrosis mutations involve residues that form polar interactions between N-terminus, transmembrane domain and CBS2, like R286Q, R762Q, R762L and R767Q [5,6]. From these findings, Zhang et al. concluded that the common gate in ClC-7 relies on an extensive interaction among different protein region, including the dimer interface, and that this increases the kinetic barrier for the voltage activation of the common gate. In such a model, osteopetrosis mutations affecting this interaction and decreasing the energy barrier would result in faster kinetics [5]. In relation to the genotype–phenotype correlation of ARO, Di Zanni et al. observed that some ARO mutations associated with neurodegeneration (R126H, A299V/E, P582H and G780R) reduced lysosomal localization and produced no or little current when expressed at the plasma membrane. In contrast to this, ARO mutations without neurodegeneration (L90P, P376L, A511T, G780W/R, A590T and R791C) preserved ion transport activity [102]. While these are interesting observations, it should be kept in mind that the protein localization is often altered by overexpression in heterologous systems. Moreover, the mechanism of dominance in ADO II is not yet firmly established. It might derive from a dominant negative effect of the mutated subunit on the kinetics of the dimeric protein (gain-of-function) similar to the mechanism by which heterozygous mutations in the muscle channel ClC-1 cause dominant (Thomsen) myotonia [120]. However, the dominant effect could be exerted also through a loss-of-function, by hampering the correct localization of the dimer or its stability. For example, while the mutations R762Q [11] and Y746Q [103] both cause an accelerated kinetics, for R762Q, the protein was unstable in patient-derived fibroblasts [7], whereas Y746Q has normal expression level and lysosomal localization [103]. Another layer of complications might be conferred by the discovery that ClC-7 binds ATP and lipids [6]. In this respect, it is interesting to note that several mutations leading to osteopetrosis (Gly765, Leu766, Arg767) map on CBS2 near the ATP-binding site [6] (Table 1 and Figure 2). It is possible to speculate that the different phenotypes of R767 mutations, with R767P and R767W displaying almost no functional activity and R767Q displaying faster activation kinetics might be due to a different impact of the mutations on gating and/or ATP binding. Mutation of Tyr715, located near the PI3P binding site, causes a novel lipid storage disease without osteopetrosis [78]. At the functional level the mutation produces a gain-of-function with increased current level and hyper-acidification of the lysosomes, but no major changes in current kinetics. In conclusion, the mechanism explaining why both gain-of-function and loss-of-function mutations of ClC-7 cause osteopetrosis and why mutations affecting the common gate cause both ARO and ADO remains to be elucidated. The great progress achieved in the electrophysiological investigation of ClC-7 when expressed at the plasma membrane will be ideally combined in the future with techniques that allow to study its properties in its physiological location, the lysosomal membrane, to better understand its contribution to the organellar ionic homeostasis.

Funding

This research received no external funding.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Jentsch, T.J.; Pusch, M. CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease. Physiol. Rev. 2018, 98, 1493–1590. [Google Scholar] [CrossRef]
  2. Zifarelli, G.; Pusch, M. CLC chloride channels and transporters: A biophysical and physiological perspective. Rev. Physiol. Biochem. Pharmacol. 2006, 158, 23–76. [Google Scholar] [CrossRef]
  3. Brandt, S.; Jentsch, T. ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family. FEBS Lett. 1995, 377, 15–20. [Google Scholar] [CrossRef]
  4. Zifarelli, G.; Pusch, M. CLC transport proteins in plants. FEBS Lett. 2009, 584, 2122–2127. [Google Scholar] [CrossRef] [PubMed]
  5. Zhang, S.; Liu, Y.; Zhang, B.; Zhou, J.; Li, T.; Liu, Z.; Li, Y.; Yang, M. Molecular insights into the human CLC-7/Ostm1 transporter. Sci. Adv. 2020, 6, eabb4747. [Google Scholar] [CrossRef] [PubMed]
  6. Schrecker, M.; Korobenko, J.; Hite, R.K. Cryo-EM structure of the lysosomal chloride-proton exchanger CLC-7 in complex with OSTM1. eLife 2020, 9, 9. [Google Scholar] [CrossRef] [PubMed]
  7. Kornak, U.; Kasper, D.; Bösl, M.R.; Kaiser, E.; Schweizer, M.; Schulz, A.; Friedrich, W.; Delling, G.; Jentsch, T.J. Loss of the ClC-7 Chloride Channel Leads to Osteopetrosis in Mice and Man. Cell 2001, 104, 205–215. [Google Scholar] [CrossRef]
  8. Kasper, D.; Planells-Cases, R.; Fuhrmann, J.; Scheel, O.; Zeitz, O.; Ruether, K.; Schmitt, A.; Poët, M.; Steinfeld, R.; Schweizer, M.; et al. Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration. EMBO J. 2005, 24, 1079–1091. [Google Scholar] [CrossRef] [PubMed]
  9. Fuhrmann, J.C.; Lange, P.F.; Wartosch, L.; Jentsch, T.J. ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function. GBM Annu. Spring Meet. Mosb. 2007, 2007, 220–223. [Google Scholar] [CrossRef]
  10. Chalhoub, N.; Benachenhou, N.; Rajapurohitam, V.; Pata, M.; Ferron, M.; Frattini, A.; Villa, A.; Vacher, J. Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. Nat. Med. 2003, 9, 399–406. [Google Scholar] [CrossRef] [PubMed]
  11. Leisle, L.; Ludwig, C.F.; Wagner, F.A.; Jentsch, T.J.; Stauber, T. ClC-7 is a slowly voltage-gated 2Cl(-)/1H(+)-exchanger and requires Ostm1 for transport activity. EMBO J. 2011, 30, 2140–2152. [Google Scholar] [CrossRef]
  12. Graves, A.R.; Curran, P.K.; Smith, C.L.; Mindell, J.A. The Cl-/H+ antiporter ClC-7 is the primary chloride permeation pathway in lysosomes. Nature 2008, 453, 788–792. [Google Scholar] [CrossRef] [PubMed]
  13. Weinert, S.; Jabs, S.; Supanchart, C.; Schweizer, M.; Gimber, N.; Richter, M.; Rademann, J.; Stauber, T.; Kornak, U.; Jentsch, T.J. Lysosomal Pathology and Osteopetrosis upon Loss of H + -Driven Lysosomal Cl—Accumulation. Science 2010, 328, 1401–1403. [Google Scholar] [CrossRef]
  14. Zifarelli, G. A tale of two CLCs: Biophysical insights toward understanding ClC-5 and ClC-7 function in endosomes and lysosomes. J. Physiol. 2015, 593, 4139–4150. [Google Scholar] [CrossRef]
  15. Wartosch, L.; Fuhrmann, J.C.; Schweizer, M.; Stauber, T.; Jentsch, T.J. Lysosomal degradation of endocytosed proteins depends on the chloride transport protein ClC-7. FASEB J. 2009, 23, 4056–4068. [Google Scholar] [CrossRef] [PubMed]
  16. Bose, S.; He, H.; Stauber, T. Neurodegeneration Upon Dysfunction of Endosomal/Lysosomal CLC Chloride Transporters. Front. Cell Dev. Biol. 2021, 9, 639231. [Google Scholar] [CrossRef]
  17. Damkier, H.H.; Christensen, H.L.; Christensen, I.B.; Wu, Q.; Fenton, R.A.; Praetorius, J. The murine choroid plexus epithelium expresses the 2Cl(-)/H(+) exchanger ClC-7 and Na(+)/H(+) exchanger NHE6 in the luminal membrane domain. Am. J. Physiol. Cell Physiol. 2018, 314, C439–C448. [Google Scholar] [CrossRef]
  18. Piret, S.; Gorvin, C.; Trinh, A.; Taylor, J.; Lise, S.; Taylor, J.C.; Ebeling, P.R.; Thakker, R.V. Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation. Am. J. Med. Genet. Part A 2016, 170, 2988–2992. [Google Scholar] [CrossRef] [PubMed]
  19. Majumdar, A.; Capetillo-Zarate, E.; Cruz, D.; Gouras, G.K.; Maxfield, F.R. Degradation of Alzheimer’s amyloid fibrils by microglia requires delivery of ClC-7 to lysosomes. Mol. Biol. Cell 2011, 22, 1664–1676. [Google Scholar] [CrossRef]
  20. Dutzler, R.; Campbell, E.B.; Cadene, M.; Chait, B.T.; MacKinnon, R. X-ray structure of a ClC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity. Nature 2002, 415, 287–294. [Google Scholar] [CrossRef] [PubMed]
  21. Dutzler, R.; Campbell, E.B.; MacKinnon, R. Gating the Selectivity Filter in ClC Chloride Channels. Science 2003, 300, 108–112. [Google Scholar] [CrossRef]
  22. Feng, L.; Campbell, E.B.; Hsiung, Y.; MacKinnon, R. Structure of a Eukaryotic CLC Transporter Defines an Intermediate State in the Transport Cycle. Science 2010, 330, 635–641. [Google Scholar] [CrossRef]
  23. Park, E.; Campbell, E.B.; MacKinnon, E.P.E.B.C.R. Structure of a CLC chloride ion channel by cryo-electron microscopy. Nat. Cell Biol. 2017, 541, 500–505. [Google Scholar] [CrossRef]
  24. Park, E.; MacKinnon, R. Structure of the CLC-1 chloride channel from Homo sapiens. eLife 2018, 7, e36629. [Google Scholar] [CrossRef]
  25. Wang, K.; Preisler, S.S.; Zhang, L.; Cui, Y.; Missel, J.W.; Grønberg, C.; Gotfryd, K.; Lindahl, E.; Andersson, M.; Calloe, K.; et al. Structure of the human ClC-1 chloride channel. PLoS Biol. 2019, 17, e3000218. [Google Scholar] [CrossRef]
  26. Han, W.; Cheng, R.C.; Maduke, M.C.; Tajkhorshid, E. Water access points and hydration pathways in CLC H+/Cl- transporters. Proc. Natl. Acad. Sci. USA 2014, 111, 1819–1824. [Google Scholar] [CrossRef]
  27. Leisle, L.; Xu, Y.; Fortea, E.; Lee, S.; Galpin, J.D.; Vien, M.; Ahern, C.A.; Accardi, A.; Bernèche, S. Divergent Cl- and H+ pathways underlie transport coupling and gating in CLC exchangers and channels. eLife 2020, 9, 9. [Google Scholar] [CrossRef]
  28. Wang, D.; Voth, G.A. Proton transport pathway in the ClC Cl-/H+ antiporter. Biophys. J. 2009, 97, 121–131. [Google Scholar] [CrossRef]
  29. Meyer, S.; Savaresi, S.; Forster, I.C.; Dutzler, R. Nucleotide recognition by the cytoplasmic domain of the human chloride transporter ClC-5. Nat. Struct. Mol. Biol. 2007, 14, 60–67. [Google Scholar] [CrossRef]
  30. Accardi, A.; Miller, C. Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels. Nature 2004, 427, 803–807. [Google Scholar] [CrossRef]
  31. Zifarelli, G.; Pusch, M. Conversion of the 2 Cl(-)/1 H(+) antiporter ClC-5 in a NO(3)(-)/H(+) antiporter by a single point mutation. Embo. J. 2009, 28, 175–182. [Google Scholar] [CrossRef]
  32. Miller, C.J. ClC chloride channels viewed through a transporter lens. Nature 2006, 440, 484–489. [Google Scholar] [CrossRef]
  33. Gadsby, D.C. Ion channels versus ion pumps: The principal difference, in principle. Nat. Rev. Mol. Cell Biol. 2009, 10, 344–352. [Google Scholar] [CrossRef]
  34. Accardi, A.; Walden, M.; Nguitragool, W.; Jayaram, H.; Williams, C.; Miller, C. Separate ion pathways in a Cl-/H+ exchanger. J. Gen. Physiol. 2005, 126, 563–570. [Google Scholar] [CrossRef]
  35. Lim, H.H.; Shane, T.; Miller, C. Intracellular proton access in a Cl(-)/H(+) antiporter. PLoS Biol. 2012, 10, e1001441. [Google Scholar] [CrossRef]
  36. Chavan, T.S.; Cheng, R.C.; Jiang, T.; Mathews, I.I.; Stein, R.A.; Koehl, A.; Mchaourab, H.S.; Tajkhorshid, E.; Maduke, M. A CLC-ec1 mutant reveals global conformational change and suggests a unifying mechanism for the CLC Cl(-)/H(+) transport cycle. eLife 2020, 9, e53479. [Google Scholar] [CrossRef]
  37. Picollo, A.; Malvezzi, M.; Houtman, J.; Accardi, A. Basis of substrate binding and conservation of selectivity in the CLC family of channels and transporters. Nat. Struct. Mol. Biol. 2009, 16, 1294–1301. [Google Scholar] [CrossRef]
  38. Bergsdorf, E.-Y.; Zdebik, A.A.; Jentsch, T.J. Residues Important for Nitrate/Proton Coupling in Plant and Mammalian CLC Transporters. J. Biol. Chem. 2009, 284, 11184–11193. [Google Scholar] [CrossRef]
  39. Feng, L.; Campbell, E.B.; MacKinnon, R. Molecular mechanism of proton transport in CLC Cl-/H+ exchange transporters. Proc. Natl. Acad. Sci. USA. 2012, 109, 11699–11704. [Google Scholar] [CrossRef]
  40. Stauber, T.; Jentsch, T.J. Sorting Motifs of the Endosomal/Lysosomal CLC Chloride Transporters. J. Biol. Chem. 2010, 285, 34537–34548. [Google Scholar] [CrossRef]
  41. Pusch, M.; Zifarelli, G. Large transient capacitive currents in wild-type lysosomal Cl-/H+ antiporter ClC-7 and residual transport activity in the proton glutamate mutant E312A. J. Gen. Physiol. 2021, 153, e202012583. [Google Scholar] [CrossRef]
  42. Zdebik, A.A.; Zifarelli, G.; Bergsdorf, E.-Y.; Soliani, P.; Scheel, O.; Jentsch, T.; Pusch, M. Determinants of Anion-Proton Coupling in Mammalian Endosomal CLC Proteins. J. Biol. Chem. 2008, 283, 4219–4227. [Google Scholar] [CrossRef]
  43. Neagoe, I.; Stauber, T.; Fidzinski, P.; Bergsdorf, E.-Y.; Jentsch, T.J. The Late Endosomal ClC-6 Mediates Proton/Chloride Countertransport in Heterologous Plasma Membrane Expression. J. Biol. Chem. 2010, 285, 21689–21697. [Google Scholar] [CrossRef]
  44. Guzman, R.E.; Grieschat, M.; Fahlke, C.; Alekov, A.K. ClC-3 Is an Intracellular Chloride/Proton Exchanger with Large Voltage-Dependent Nonlinear Capacitance. ACS Chem. Neurosci. 2013, 4, 994–1003. [Google Scholar] [CrossRef][Green Version]
  45. Weinert, S.; Jabs, S.; Hohensee, S.; Chan, W.L.; Kornak, U.; Jentsch, T.J. Transport activity and presence of ClC-7/Ostm1 complex account for different cellular functions. EMBO Rep. 2014, 15, 784–791. [Google Scholar] [CrossRef]
  46. Smith, A.J.; Lippiat, J.D. Voltage-dependent charge movement associated with activation of the CLC-5 2Cl-/1H+ exchanger. Faseb. J. 2010, 24, 3696–3705. [Google Scholar] [CrossRef]
  47. Alekov, A.; Fahlke, C. Channel-like slippage modes in the human anion/proton exchanger ClC-4. J. Gen. Physiol. 2009, 133, 485–496. [Google Scholar] [CrossRef]
  48. Zifarelli, G.; De Stefano, S.; Zanardi, I.; Pusch, M. On the Mechanism of Gating Charge Movement of ClC-5, a Human Cl−/H+ Antiporter. Biophys. J. 2012, 102, 2060–2069. [Google Scholar] [CrossRef][Green Version]
  49. De Stefano, S.; Pusch, M.; Zifarelli, G. A single point mutation reveals gating of the human ClC-5 Cl-/H+ antiporter. J. Physiol. 2013, 591, 5879–5893. [Google Scholar] [CrossRef]
  50. Sobacchi, C.; Schulz, A.; Coxon, F.P.; Villa, A.; Helfrich, M.H. Osteopetrosis: Genetics, treatment and new insights into osteoclast function. Nat. Rev. Endocrinol. 2013, 9, 522–536. [Google Scholar] [CrossRef]
  51. Henriksen, K.; Bollerslev, J.; Everts, V.; Karsdal, M.A. Osteoclast Activity and Subtypes as a Function of Physiology and Pathology—Implications for Future Treatments of Osteoporosis. Endocr. Rev. 2011, 32, 31–63. [Google Scholar] [CrossRef]
  52. Frattini, A.; Pangrazio, A.; Susani, L.; Sobacchi, C.; Mirolo, M.; Abinun, M.; Andolina, M.; Flanagan, A.; Horwitz, E.M.; Mihci, E.; et al. Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis. J. Bone Miner. Res. 2003, 18, 1740–1747. [Google Scholar] [CrossRef]
  53. Balemans, W.; Van Wesenbeeck, L.; Van Hul, W. A Clinical and Molecular Overview of the Human Osteopetroses. Calcif. Tissue Int. 2005, 77, 263–274. [Google Scholar] [CrossRef]
  54. Cleiren, E.; Bénichou, O.; Van Hul, E.; Gram, J.; Bollerslev, J.; Singer, F.R.; Beaverson, K.; Aledo, A.; Whyte, M.P.; Yoneyama, T.; et al. Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum. Mol. Genet. 2001, 10, 2861–2867. [Google Scholar] [CrossRef] [PubMed]
  55. Benichou, O.D.; Bénichou, B.; Copin, H.; De Vernejoul, M.C.; Van Hul, W. Further Evidence for Genetic Heterogeneity Within Type II Autosomal Dominant Osteopetrosis. J. Bone Miner. Res. 2000, 15, 1900–1904. [Google Scholar] [CrossRef]
  56. Bollerslev, J.; Andersen, P. Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis. Bone 1988, 9, 7–13. [Google Scholar] [CrossRef]
  57. Maurizi, A.; Capulli, M.; Curle, A.; Patel, R.; Ucci, A.; Côrtes, J.A.; Oxford, H.; Lamandé, S.R.; Bateman, J.F.; Rucci, N.; et al. Extra-skeletal manifestations in mice affected by Clcn7-dependent autosomal dominant osteopetrosis type 2 clinical and therapeutic implications. Bone Res. 2019, 7, 17. [Google Scholar] [CrossRef] [PubMed]
  58. Kida, Y.; Uchida, S.; Miyazaki, H.; Sasaki, S.; Marumo, F. Localization of mouse CLC-6 and CLC-7 mRNA and their functional complementation of yeast CLC gene mutant. Histochem. Cell Biol. 2001, 115, 189–194. [Google Scholar] [CrossRef]
  59. Hiroyama, Y.; Miike, T.; Sugino, S.; Taku, K. Creatine kinase brain isoenzyme in infantile osteopetrosis. Pediatr. Neurol. 1987, 3, 54–57. [Google Scholar] [CrossRef]
  60. Rössler, U.; Hennig, A.F.; Stelzer, N.; Bose, S.; Kopp, J.; Søe, K.; Cyganek, L.; Zifarelli, G.; Ali, S.; von der Hagen, M.; et al. Efficient generation of osteoclasts from human induced pluripotent stem cells and functional investigations of lethal CLCN7 -related osteopetrosis. J. Bone Miner. Res. 2021, 36, 1621–1635. [Google Scholar] [CrossRef]
  61. Teinert, J.; Behne, R.; Wimmer, M.; Ebrahimi-Fakhari, D. Novel insights into the clinical and molecular spectrum of congenital disorders of autophagy. J. Inherit. Metab. Dis. 2019, 43, 51–62. [Google Scholar] [CrossRef] [PubMed]
  62. Ryter, S.W.; Bhatia, D.; Choi, M.E. Autophagy: A Lysosome-Dependent Process with Implications in Cellular Redox Homeostasis and Human Disease. Antioxid. Redox Signal. 2019, 30, 138–159. [Google Scholar] [CrossRef]
  63. Pata, M.; Vacher, J. Ostm1 Bifunctional Roles in Osteoclast Maturation: Insights From a Mouse Model Mimicking a Human OSTM1 Mutation. J. Bone Miner. Res. 2018, 33, 888–898. [Google Scholar] [CrossRef] [PubMed]
  64. Neutzsky-Wulff, A.; Sims, N.; Supanchart, C.; Kornak, U.; Felsenberg, D.; Poulton, I.; Martin, T.; Karsdal, M.; Henriksen, K. Severe developmental bone phenotype in ClC-7 deficient mice. Dev. Biol. 2010, 344, 1001–1010. [Google Scholar] [CrossRef] [PubMed]
  65. Sobacchi, C.; Villa, A.; Schulz, A.; Kornak, U. CLCN7-related Osteopetrosis. In GeneReviews(R); Pagon, R.A., Adam, M.P., Ardinger, H.H., Wallace, S.E., Amemiya, A., Bean, L.J.H., Bird, T.D., Ledbetter, N., Mefford, H.C., Smith, R.J.H., et al., Eds.; University of Washington: Seattle, WA, USA, 2022. [Google Scholar]
  66. Pangrazio, A.; Poliani, P.L.; Megarbane, A.; Lefranc, G.; Lanino, E.; Di Rocco, M.; Rucci, F.; Lucchini, F.; Ravanini, M.; Facchetti, F.; et al. Mutations in OSTM1 (Grey Lethal) Define a Particularly Severe Form of Autosomal Recessive Osteopetrosis With Neural Involvement. J. Bone Miner. Res. 2006, 21, 1098–1105. [Google Scholar] [CrossRef]
  67. Gerritsen, E.J.; Vossen, J.M.; Van Loo, I.H.; Hermans, J.; Helfrich, M.H.; Griscelli, C.; Fischer, A. Autosomal recessive osteopetrosis: Variability of findings at diagnosis and during the natural course. Pediatrics 1994, 93, 247–253. [Google Scholar] [CrossRef]
  68. Mazzolari, E.; Forino, C.; Razza, A.; Porta, F.; Villa, A.; Notarangelo, L.D. A single-center experience in 20 patients with infantile malignant osteopetrosis. Am. J. Hematol. 2009, 84, 473–479. [Google Scholar] [CrossRef] [PubMed]
  69. Teti, A.; Econs, M.J. Osteopetroses, emphasizing potential approaches to treatment. Bone 2017, 102, 50–59. [Google Scholar] [CrossRef]
  70. Campos-Xavier, A.B.; Casanova, J.-L.; Doumaz, Y.; Feingold, J.; Munnich, A.; Cormier-Daire, V. Intrafamilial phenotypic variability of osteopetrosis due to chloride channel 7 (CLCN7) mutations. Am. J. Med Genet. Part A 2005, 133A, 216–218. [Google Scholar] [CrossRef]
  71. Pang, Q.; Chi, Y.; Zhao, Z.; Xing, X.; Li, M.; Wang, O.; Jiang, Y.; Liao, R.; Sun, Y.; Dong, J.; et al. Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients. Osteoporos. Int. 2015, 27, 1047–1055. [Google Scholar] [CrossRef] [PubMed]
  72. Pangrazio, A.; Pusch, M.; Caldana, E.; Frattini, A.; Lanino, E.; Tamhankar, P.M.; Phadke, S.; Lopez, A.G.M.; Orchard, P.; Mihci, E.; et al. Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: Report of 20 novel mutations. Hum. Mutat. 2010, 31, E1071–E1080. [Google Scholar] [CrossRef]
  73. Letizia, C.; Taranta, A.; Migliaccio, S.; Caliumi, C.; Diacinti, D.; Delfini, E.; D’Erasmo, E.; Iacobini, M.; Roggini, M.; Albagha, O.M.E.; et al. Type II Benign Osteopetrosis (Albers-Schönberg Disease) Caused by a Novel Mutation in CLCN7 Presenting with Unusual Clinical Manifestations. Calcif. Tissue Int. 2003, 74, 42–46. [Google Scholar] [CrossRef] [PubMed]
  74. Del Fattore, A.; Peruzzi, B.; Rucci, N.; Recchia, I.; Cappariello, A.; Longo, M.; Fortunati, D.; Ballanti, P.; Iacobini, M.; Luciani, M.; et al. Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: Implications for diagnosis and treatment. J. Med Genet. 2005, 43, 315–325. [Google Scholar] [CrossRef] [PubMed][Green Version]
  75. Waguespack, S.G.; Hui, S.L.; DiMeglio, L.; Econs, M. Autosomal Dominant Osteopetrosis: Clinical Severity and Natural History of 94 Subjects with a Chloride Channel 7 Gene Mutation. J. Clin. Endocrinol. Metab. 2007, 92, 771–778. [Google Scholar] [CrossRef]
  76. Campos-Xavier, A.; Saraiva, J.M.; Ribeiro, L.M.; Munnich, A.; Cormier-Daire, V. Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis. Hum. Genet. 2003, 112, 186–189. [Google Scholar] [CrossRef] [PubMed]
  77. Xue, Y.; Wang, W.; Mao, T.; Duan, X. Report of two Chinese patients suffering from CLCN7-related osteopetrosis and root dysplasia. J. Cranio-Maxillofac. Surg. 2012, 40, 416–420. [Google Scholar] [CrossRef] [PubMed]
  78. Nicoli, E.-R.; Weston, M.R.; Hackbarth, M.; Becerril, A.; Larson, A.; Zein, W.M.; Baker, P.R.; Burke, J.D.; Dorward, H.; Davids, M.; et al. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification. Am. J. Hum. Genet. 2019, 104, 1127–1138. [Google Scholar] [CrossRef]
  79. Xu, H.; Ren, D. Lysosomal Physiology. Annu. Rev. Physiol. 2015, 77, 57–80. [Google Scholar] [CrossRef]
  80. Li, P.; Gu, M.; Xu, H. Lysosomal Ion Channels as Decoders of Cellular Signals. Trends Biochem. Sci. 2019, 44, 110–124. [Google Scholar] [CrossRef]
  81. Ishida, Y.; Nayak, S.; Mindell, J.A.; Grabe, M. A model of lysosomal pH regulation. J. Gen. Physiol. 2013, 141, 705–720. [Google Scholar] [CrossRef]
  82. Astaburuaga, R.; Haro, O.D.Q.; Stauber, T.; Relόgio, A. A Mathematical Model of Lysosomal Ion Homeostasis Points to Differential Effects of Cl− Transport in Ca2+ Dynamics. Cells 2019, 8, 1263. [Google Scholar] [CrossRef]
  83. Steinberg, B.E.; Huynh, K.K.; Brodovitch, A.; Jabs, S.; Stauber, T.; Jentsch, T.J.; Grinstein, S. A cation counterflux supports lysosomal acidification. J. Cell Biol. 2010, 189, 1171–1186. [Google Scholar] [CrossRef] [PubMed]
  84. Van Dyke, R.W. Acidification of rat liver lysosomes: Quantitation and comparison with endosomes. Am. J. Physiol. Content 1993, 265, 901–917. [Google Scholar] [CrossRef] [PubMed]
  85. Moriyama, Y. Potassium ion dependent proton efflux and depolarization from spleen lysosomes. Biochem. Biophys. Res. Commun. 1988, 156, 211–216. [Google Scholar] [CrossRef]
  86. Marcoline, F.; Ishida, Y.; Mindell, J.; Nayak, S.; Grabe, M. A mathematical model of osteoclast acidification during bone resorption. Bone 2016, 93, 167–180. [Google Scholar] [CrossRef] [PubMed]
  87. Alam, I.; Gray, A.K.; Chu, K.; Ichikawa, S.; Mohammad, K.S.; Capannolo, M.; Capulli, M.; Maurizi, A.; Muraca, M.; Teti, A.; et al. Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models. Bone 2014, 59, 66–75. [Google Scholar] [CrossRef]
  88. Caetano-Lopes, J.; Lessard, S.; Hann, S.; Espinoza, K.; Kang, K.; Lim, K.; Horan, D.; Noonan, H.; Hu, D.; Baron, R.; et al. Clcn7F318L/+ as a new mouse model of Albers-Schönberg disease. Bone 2017, 105, 253–261. [Google Scholar] [CrossRef] [PubMed]
  89. Chu, K.; Koller, D.L.; Snyder, R.; Fishburn, T.; Lai, D.; Waguespack, S.G.; Foroud, T.; Econs, M.J. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: Searching for modifier genes. Bone 2005, 37, 655–661. [Google Scholar] [CrossRef] [PubMed]
  90. Steward, C.G. Neurological aspects of osteopetrosis. Neuropathol. Appl. Neurobiol. 2003, 29, 87–97. [Google Scholar] [CrossRef]
  91. Pressey, S.N.; O’Donnell, K.J.; Stauber, T.; Fuhrmann, J.C.; Tyynelä, J.; Jentsch, T.J.; Cooper, J.D. Distinct neuropathologic phenotypes after disrupting the chloride transport proteins ClC-6 or ClC-7/Ostm1. J. Neuropathol. Exp. Neurol. 2010, 69, 1228–1246. [Google Scholar] [CrossRef]
  92. Ohmi, K.; Greenberg, D.S.; Rajavel, K.S.; Ryazantsev, S.; Li, H.H.; Neufeld, E.F. Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB. Proc. Natl. Acad. Sci. USA 2003, 100, 1902–1907. [Google Scholar] [CrossRef]
  93. Wada, R.; Tifft, C.J.; Proia, R.L. Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation. Proc. Natl. Acad. Sci. USA 2000, 97, 10954–10959. [Google Scholar] [CrossRef]
  94. Kornak, U.; Schulz, A.; Friedrich, W.; Uhlhaas, S.; Kremens, B.; Voit, T.; Hasan, C.; Bode, U.; Jentsch, T.J.; Kubisch, C. Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis. Hum. Mol. Genet. 2000, 9, 2059–2063. [Google Scholar] [CrossRef]
  95. Frattini, A.; Orchard, P.J.; Sobacchi, C.; Giliani, S.; Abinun, M.; Mattsson, J.P.; Keeling, D.J.; Andersson, A.-K.; Wallbrandt, P.; Zecca, L.; et al. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. Nat. Genet. 2000, 25, 343–346. [Google Scholar] [CrossRef]
  96. Wartosch, L.; Stauber, T. A role for chloride transport in lysosomal protein degradation. Autophagy 2010, 6, 158–159. [Google Scholar] [CrossRef] [PubMed]
  97. Prinetti, A.; Rocchetta, F.; Costantino, E.; Frattini, A.; Caldana, E.; Rucci, F.; Bettiga, A.; Poliani, P.L.; Chigorno, V.; Sonnino, S. Brain lipid composition in grey-lethal mutant mouse characterized by severe malignant osteopetrosis. Glycoconj. J. 2008, 26, 623–633. [Google Scholar] [CrossRef] [PubMed]
  98. Poet, M.; Kornak, U.; Schweizer, M.; Zdebik, A.A.; Scheel, O.; Hoelter, S.; Wurst, W.; Schmitt, A.; Fuhrmann, J.; Planells-Cases, R.; et al. Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6. Proc. Natl. Acad. Sci. USA 2006, 103, 13854–13859. [Google Scholar] [CrossRef]
  99. Stauber, T.; Weinert, S.; Jentsch, T.J. Cell Biology and Physiology of CLC Chloride Channels and Transporters. Compr. Physiol. 2012, 2, 1701–1744. [Google Scholar] [CrossRef]
  100. Polovitskaya, M.M.; Barbini, C.; Martinelli, D.; Harms, F.L.; Cole, F.S.; Calligari, P.; Bocchinfuso, G.; Stella, L.; Ciolfi, A.; Niceta, M.; et al. A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl−/H+-Exchanger, Causes Early-Onset Neurodegeneration. Am. J. Hum. Genet. 2020, 107, 1062–1077. [Google Scholar] [CrossRef] [PubMed]
  101. He, H.; Cao, X.; Yin, F.; Wu, T.; Stauber, T.; Peng, J. West Syndrome Caused By a Chloride/Proton Exchange-Uncoupling CLCN6 Mutation Related to Autophagic-Lysosomal Dysfunction. Mol. Neurobiol. 2021, 58, 2990–2999. [Google Scholar] [CrossRef]
  102. Di Zanni, E.; Palagano, E.; Lagostena, L.; Strina, D.; Rehman, A.; Abinun, M.; De Somer, L.; Martire, B.; Brown, J.; Kariminejad, A.; et al. Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC -7 Mutants. J. Bone Miner. Res. 2021, 36, 531–545. [Google Scholar] [CrossRef]
  103. Sartelet, A.; Stauber, T.; Coppieters, W.; Ludwig, C.F.; Fasquelle, C.; Druet, T.; Zhang, Z.; Ahariz, N.; Cambisano, N.; Jentsch, T.J.; et al. A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle. Dis. Model Mech. 2014, 7, 119–128. [Google Scholar] [CrossRef]
  104. Ludwig, C.F.; Ullrich, F.; Leisle, L.; Stauber, T.; Jentsch, T.J. Common gating of both CLC transporter subunits underlies voltage-dependent activation of the 2Cl-/1H+ exchanger ClC-7/Ostm1. J. Biol. Chem. 2013, 288, 28611–28619. [Google Scholar] [CrossRef]
  105. Bykova, E.A.; Zhang, X.-D.; Chen, T.-Y.; Zheng, J. Large movement in the C terminus of CLC-0 chloride channel during slow gating. Nat. Struct. Mol. Biol. 2006, 13, 1115–1119. [Google Scholar] [CrossRef]
  106. Wang, C.; Zhang, H.; He, J.-W.; Gu, J.-M.; Hu, W.-W.; Hu, Y.-Q.; Li, M.; Liu, Y.-J.; Fu, W.-Z.; Yue, H.; et al. The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: Six novel mutations of the CLCN7 gene in twelve osteopetrosis families. J. Bone Miner. Metab. 2011, 30, 338–348. [Google Scholar] [CrossRef] [PubMed]
  107. Barvencik, F.; Kurth, I.; Koehne, T.; Stauber, T.; Zustin, J.; Tsiakas, K.; Ludwig, C.F.; Beil, F.T.; Pestka, J.M.; Hahn, M.; et al. CLCN7andTCIRG1Mutations Differentially Affect Bone Matrix Mineralization in Osteopetrotic Individuals. J. Bone Miner. Res. 2013, 29, 982–991. [Google Scholar] [CrossRef]
  108. Waguespack, S.G.; Koller, D.L.; White, K.E.; Fishburn, T.; Carn, G.; Buckwalter, K.A.; Johnson, M.; Kocisko, M.; Evans, W.E.; Foroud, T.; et al. Chloride Channel 7 (ClCN7) Gene Mutations and Autosomal Dominant Osteopetrosis, Type II. J. Bone Miner. Res. 2003, 18, 1513–1518. [Google Scholar] [CrossRef] [PubMed]
  109. Henriksen, K.; Gram, J.; Schaller, S.; Dahl, B.H.; Dziegiel, M.H.; Bollerslev, J.; Karsdal, M.A. Characterization of Osteoclasts from Patients Harboring a G215R Mutation in ClC-7 Causing Autosomal Dominant Osteopetrosis Type II. Am. J. Pathol. 2004, 164, 1537–1545. [Google Scholar] [CrossRef]
  110. Schulz, P.; Werner, J.; Stauber, T.; Henriksen, K.; Fendler, K. The G215R mutation in the Cl-/H+-antiporter ClC-7 found in ADO II osteopetrosis does not abolish function but causes a severe trafficking defect. PLoS ONE 2010, 5, e12585. [Google Scholar] [CrossRef]
  111. Zhang, X.; Wei, Z.; He, J.; Wang, C.; Zhang, Z. Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families. Postgrad. Med. 2017, 129, 934–942. [Google Scholar] [CrossRef] [PubMed]
  112. Lam, C.-W.; Tong, S.-F.; Wong, K.; Luo, Y.F.; Tang, H.-Y.; Ha, S.-Y.; Chan, M.H.-M. DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: Standardization of molecular investigations of genetic diseases due to consanguinity. J. Hum. Genet. 2007, 52, 98–101. [Google Scholar] [CrossRef]
  113. Bonapace, G.; Moricca, M.T.; Talarico, V.; Graziano, F.; Pensabene, L.; Miniero, R. Identification of two novel mutations on CLCN7 gene in a patient with malignant ostopetrosis. Ital. J. Pediatr. 2014, 40, 90. [Google Scholar] [CrossRef][Green Version]
  114. Zheng, H.; Shao, C.; Zheng, Y.; He, J.-W.; Fu, W.-Z.; Wang, C.; Zhang, Z.-L. Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II). J. Bone Miner. Metab. 2015, 34, 440–446. [Google Scholar] [CrossRef]
  115. Phadke, S.R.; Fischer, B.; Gupta, N.; Ranganath, P.; Kabra, M.; Kornak, U. Novel mutations in Indian patients with autosomal recessive infantile malignant osteopetrosis. Indian J. Med Res. 2010, 131, 508–514. [Google Scholar]
  116. Zeng, B.; Li, R.; Hu, Y.; Hu, B.; Zhao, Q.; Liu, H.; Yuan, P.; Wang, Y. A novel mutation and a known mutation in the CLCN7 gene associated with relatively stable infantile malignant osteopetrosis in a Chinese patient. Gene 2016, 576, 176–181. [Google Scholar] [CrossRef] [PubMed]
  117. Rashid, B.M.; Rashid, N.G.; Schulz, A.; Lahr, G.; Nore, B.F. A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: A case series. J. Med Case Rep. 2013, 7, 7. [Google Scholar] [CrossRef] [PubMed]
  118. Okamoto, N.; Kohmoto, T.; Naruto, T.; Masuda, K.; Komori, T.; Imoto, I. Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis. Hum. Genome Var. 2017, 4, 17036. [Google Scholar] [CrossRef] [PubMed]
  119. Besbas, N.; Draaken, M.; Ludwig, M.; Deren, O.; Orhan, D.; Bilginer, Y.; Ozaltin, F. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis. Eur. J. Nucl. Med. Mol. Imaging 2009, 168, 1449–1454. [Google Scholar] [CrossRef] [PubMed]
  120. Pusch, M. Myotonia caused by mutations in the muscle chloride channel geneCLCN1. Hum. Mutat. 2002, 19, 423–434. [Google Scholar] [CrossRef]
Cells 11 00366 g001
Figure 1. (A) Topology diagram of ClC-7. (B) Structure of the hClC-7/Ostm1 complex. Structure of the hClC-7/Ostm1 complex based on the work of Schrecker et al. (PDB entry 7JM7) viewed from the membrane plane [6]. The two ClC-7 subunits are represented in grey and green, the two Ostm1 subunits in orange and cyan. The blue arrows indicate the three anion binding sites in the permeation pathway (magenta spheres) and the location of the lipid and of the Mg-ATP (only in the green subunit). The cytosolic C-terminal region of the protein comprises two so called CBS (cystathionine β synthase) domains.
Figure 1. (A) Topology diagram of ClC-7. (B) Structure of the hClC-7/Ostm1 complex. Structure of the hClC-7/Ostm1 complex based on the work of Schrecker et al. (PDB entry 7JM7) viewed from the membrane plane [6]. The two ClC-7 subunits are represented in grey and green, the two Ostm1 subunits in orange and cyan. The blue arrows indicate the three anion binding sites in the permeation pathway (magenta spheres) and the location of the lipid and of the Mg-ATP (only in the green subunit). The cytosolic C-terminal region of the protein comprises two so called CBS (cystathionine β synthase) domains.
Cells 11 00366 g001
Cells 11 00366 g002
Figure 2. Simplified model of the transport cycle of CLC transporters based on the work of Leisle et al. [27]. Cl− ions at the external and central binding sites are represented as blue circles, H+ are represented as red circles, the anion permeation pathway is shown in pale blue, the H+ permeation pathway in green. The gating and proton glutamates and the phenyalanine residues are explicitly indicated in the figure. (a) The gating glutamate is oriented towards the extracellular space and its side chain protonated. Cl− ions are present at both the external and central binding site. (b) The protonated gating glutamate rotates towards the interior of the protein along a pathway defined by two phenylalanine residues. (c) The protonated gating glutamate continues its movement towards the central binding site displacing a Cl− ion towards the extracellular space. (d) The H+ dissociates from the side chain of the gating glutamate. (e) The H+ binds the proton glutamate and the side chain of the gating glutamate moves upwards to occupy the external anion binding site displacing a second Cl− ion. Not explicitly indicated is an intermediate state following proton release to the cytosolic side in which Cl− ions from the internal side have access to the permeation pathway.
Figure 2. Simplified model of the transport cycle of CLC transporters based on the work of Leisle et al. [27]. Cl− ions at the external and central binding sites are represented as blue circles, H+ are represented as red circles, the anion permeation pathway is shown in pale blue, the H+ permeation pathway in green. The gating and proton glutamates and the phenyalanine residues are explicitly indicated in the figure. (a) The gating glutamate is oriented towards the extracellular space and its side chain protonated. Cl− ions are present at both the external and central binding site. (b) The protonated gating glutamate rotates towards the interior of the protein along a pathway defined by two phenylalanine residues. (c) The protonated gating glutamate continues its movement towards the central binding site displacing a Cl− ion towards the extracellular space. (d) The H+ dissociates from the side chain of the gating glutamate. (e) The H+ binds the proton glutamate and the side chain of the gating glutamate moves upwards to occupy the external anion binding site displacing a second Cl− ion. Not explicitly indicated is an intermediate state following proton release to the cytosolic side in which Cl− ions from the internal side have access to the permeation pathway.
Cells 11 00366 g002
Cells 11 00366 g003
Figure 3. Location of osteopetrosis mutations on the structure of ClC-7 (PDB entry: 7JM7). For clarity, the mutations are indicated only in the grey monomer. ARO mutations are represented by red spheres, ADO II mutations by blue spheres and IARO mutations by orange spheres (except the variants found as compound heterozygous V418M-R674Q, as they also cause ADO II when expressed alone [60]). The cyan sphere represents the mutation Y715C, causing lysosomal storage disease and albinism without osteopetrosis [68]. The magenta spheres represent the three anion binding sites in the permeation pathway.
Figure 3. Location of osteopetrosis mutations on the structure of ClC-7 (PDB entry: 7JM7). For clarity, the mutations are indicated only in the grey monomer. ARO mutations are represented by red spheres, ADO II mutations by blue spheres and IARO mutations by orange spheres (except the variants found as compound heterozygous V418M-R674Q, as they also cause ADO II when expressed alone [60]). The cyan sphere represents the mutation Y715C, causing lysosomal storage disease and albinism without osteopetrosis [68]. The magenta spheres represent the three anion binding sites in the permeation pathway.
Cells 11 00366 g003
Cells 11 00366 g004
Figure 4. Schematic representation of the role of ClC-7 in lysosomes. Lysosomal acidification results from the complex interplay of anion and cation transport mediated by different families of ion channels and transporters. ClC-7 is indicated in light blue, V-type ATPase in light red. A variety of cation channels is also indicated. The orientation of Cl− and H+ movement is suggested on the basis of the electrophysiological studies in which ClC-7 is expressed at the plasma membrane.
Figure 4. Schematic representation of the role of ClC-7 in lysosomes. Lysosomal acidification results from the complex interplay of anion and cation transport mediated by different families of ion channels and transporters. ClC-7 is indicated in light blue, V-type ATPase in light red. A variety of cation channels is also indicated. The orientation of Cl− and H+ movement is suggested on the basis of the electrophysiological studies in which ClC-7 is expressed at the plasma membrane.
Cells 11 00366 g004
Table 1. List of disease-causing CLCN7 mutations.
Table 1. List of disease-causing CLCN7 mutations.
MutationAmino Acid LocationDisease Current AmplitudeCurrent ActivationLysosomal Localization
L90P
(splice variant)		N-terminusAROnormalnormalnormal[102]
Y99CN-terminusADO II [74]
R126HHelix BARO (neurodegen.)reducedacceleratedstrongly reduced [102]
W127GHelix BADO II [106]
L132P
(L227del)		Helix BARO [72]
D145fsHelix BARO [52]
D145GHelix BADO II acceleratednormal[107]
W179xHelix CADO II [52]
G203DLoop helix C-DIARO [76]
L213FHelix D ADO IInormalaccelerated [11,108]
N214S
(R767P)		Helix DARO [72]
G215RHelix DADO II and ADO II + renal tubular acidosis ER retention[18,52,54,109,110]
L224R
(K691fs)		Helix EIARO [71]
G240E
(W127G)		Helix EARO [111]
G240R
(A299E)		Helix EARO (neurodegen.)strongly reduced reduced[11,102]
G240R
(R526W)		Helix EARO [52]
G240R
(L651P)		Helix EARO [72]
P249LHelix FADO II [54,102]
P249R
(S744F)		Helix FARO [52]
I261FHelix FARO [112]
R271xLoop helix F-GARO [72]
R280C
(splice variant)		Loop helix F-GARO [113]
R286QHelix GADO IInormalaccelerated [11,52]
R286WHelix GADO II [71,108]
V289LHelix GADO II [114]
S290FHelix GADO II [106]
S290YHelix GADO II [71]
G292E
(R403Q)		Helix GARO (neurodeg.) [60]
V297MHelix GAROstrongly reduced normal
(increased overall expression)		[52,115]
A299EHelix GARO (neurodegen.)strongly reduced strongly reduced[102,116]
A299VHelix GADO II/ARO (neurodegen.)strongly reduced strongly reduced[102]
E313KHelix HADO II [106]
A316GLoop helix H-IADO II [106]
F318LLoop helix H-IADO IIreduced normal[52,72]
F318SLoop helix H-IADO II [111]
W319RLoop helix H-IADO II [71]
L323PHelix IADO IInormalacceleratednormal [102]
R326GHelix IADO II [71]
M332V (R767W)Helix IARO [52]
G347RHelix IADO II [71]
E374x
(in frame insertion G306)		Loop helix I-JARO [52]
P376LHelix JAROreducedacceleratedstrongly reduced[102]
R403Q
(G512R)		Helix JARO [72]
R409WLoop helix J-KADO II [117]
V418MHelix KADO II [70]
V418M
(R674Q)		Helix KIARO [70]
V418fsHelix KARO [72]
P470LLoop helix K-LIARO [77]
P470QLoop helix K-LIARO [76]
S473NHelix LADO II [71]
L490FHelix MADOreduced Normal
(reduced overall expression)		[11,52]
C502Y
(V577M)		Helix MIARO [118]
A511T
(G780W)		Loop helix M-NARO [102]
G521RHelix NARO (neurodegen.)strongly reduced reduced[52]
R526QHelix NARO [72]
R526THelix NARO [72]
R526WHelix NAROstrongly reduced reduced
ER retention		[52]
L549PHelix OARO [72]
Q555x
(R762Q)		Helix OARO [7]
R561QLoop Helix O-PARO [119]
L564PHelix PADO II [71]
P582HHelix QARO (neurodegen.) reduced[102]
A590THelix QARO normal[102]
L614P
(Del exon 17) 		Loop helix R–CBS1ARO [52]
P619LLoop helix R–CBS1AROreduced [52,115]
P634fsCBS1ARO [72]
L651PCBS1AROstrongly reduced normal[52]
R674QCBS1ADO II [70]
G677VCBS1ADO II [52,54]
K689ELoop CBS1-CBS2ADO II [54]
K691ELoop CBS1-CBS2ADO IIreducedslowerreduced[102]
R712x
(E730x)		Loop CBS1-CBS2ARO [72]
Y715CLoop CBS1-CBS2Lysosomal storage + albinism [78]
G741RLoop CBS1-CBS2ADO II [106]
R743WLoop CBS1-CBS2ADO II [106]
S744FLoop CBS1-CBS2AROnormal [11,52]
Y746QCBS2ADO bovine acceleratednormal [103]
S753WCBS2ADO II [111]
F758LCBS2ADO II [72]
R762LCBS2ADO II accelerated [11,108]
R762QCBS2ARO accelerated [7,11]
R762W
(splicing variant)		CBS2ADO II [72]
L766PCBS2ARO [54]
R767PCBS2AROstrongly reduced normal (reduced overall expression)[11]
R767QCBS2AROnormalaccelerated [11,52]
R767WCBS2ADO IIStrongly reduced Normal (reduced overall expression)[11,54]
R767W
(M332V)		CBS2ARO [52]
G780R
(splice variant)		CBS2ARO (neurodegen.) [102]
A788DCBS2ADO IInormal [11,73]
R791CCBS2 AROnormalacceleratedstrongly reduced[102]
G796fsCBS2ADO II accelerated [11,54]
The table indicates the amino acid location, the specific type of osteopetrosis (ARO, ADO II and IARO), the effect of the mutation on the current amplitude and activation kinetics and on the lysosomal localization.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Zifarelli, G. The Role of the Lysosomal Cl−/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration. Cells 2022, 11, 366. https://doi.org/10.3390/cells11030366

AMA Style

Zifarelli G. The Role of the Lysosomal Cl−/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration. Cells. 2022; 11(3):366. https://doi.org/10.3390/cells11030366

Chicago/Turabian Style

Zifarelli, Giovanni. 2022. "The Role of the Lysosomal Cl−/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration" Cells 11, no. 3: 366. https://doi.org/10.3390/cells11030366

APA Style

Zifarelli, G. (2022). The Role of the Lysosomal Cl−/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration. Cells, 11(3), 366. https://doi.org/10.3390/cells11030366

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