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Int. J. Mol. Sci. 2013, 14(12), 23274-23288; doi:10.3390/ijms141223274
Published: 26 November 2013
Abstract: Mevalonic aciduria, a rare autosomal recessive disease, represents the most severe form of the periodic fever, known as Mevalonate Kinase Deficiency. This disease is caused by the mutation of the MVK gene, which codes for the enzyme mevalonate kinase, along the cholesterol pathway. Mevalonic aciduria patients show recurrent fever episodes with associated inflammatory symptoms, severe neurologic impairments, or death, in early childhood. The typical neurodegeneration occurring in mevalonic aciduria is linked both to the intrinsic apoptosis pathway (caspase-3 and -9), which is triggered by mitochondrial damage, and to pyroptosis (caspase-1). These cell death mechanisms seem to be also related to the assembly of the inflammasome, which may, in turn, activate pro-inflammatory cytokines and chemokines. Thus, this particular molecular platform may play a crucial role in neuroinflammation mechanisms. Nowadays, a specific therapy is still lacking and the pathogenic mechanisms involving neuroinflammation and neuronal dysfunction have not yet been completely understood, making mevalonic aciduria an orphan drug disease. This review aims to analyze the relationship among neuroinflammation, mitochondrial damage, programmed cell death, and neurodegeneration. Targeting inflammation and degeneration in the central nervous system might help identify promising treatment approaches for mevalonic aciduria or other diseases in which these mechanisms are involved.
Mevalonate Kinase Deficiency (MKD) is a rare, autosomic recessive, metabolic disease, caused by mutations in the MVK gene (12q24.11, NM_000431) coding for the enzyme mevalonate kinase (MK) (E.C. 188.8.131.52), the second enzyme of the mevalonate pathway, the route to cholesterol (Figure 1a) [1,2].
The severity of the disease is linked with the residual activity of MK; a residual activity between 1%–8% leads to a mild autoinflammatory phenotype, called hyper immunoglobulinemia D syndrome (HIDS, OMIM #260920), the symptoms of which are recurrent episodes of fever and associated inflammatory events. A residual activity below the level of detection leads to the most severe form of this pathology, known as mevalonic aciduria (MA, OMIM #610377), which, in addition, shows developmental delay, dysmorphic features, ataxia, cerebellar atrophy, psychomotor retardation, and sometimes death occurs in early childhood .
Although in the past decade the knowledge of the pathogenesis of MKD has increased, the link between genetic defect and phenotype is not yet clear. The most accredited pathogenic hypothesis is that the inflammatory phenotype is caused by shortage of isoprenoid compounds [4–6]. Thus far, this condition has been reproduced in biochemical experimental models obtained using drugs able to block the mevalonate pathway . The so-caused cellular damage is driven by caspase-1 alone or in conjunction with caspase-3, via pyroptosis-apoptosis . Recent data showed a pivotal role of the inflammasome platform at a systemic level , but its role in neurological impairments has never been ascertained. Finally, it has been found that the inflammasome involvement is deeply entangled with mitochondrial redox modulation [10–12].
MKD is considered today an orphan and neglected disease, and an aetiologic treatment is still unavailable. The attainment of new pharmacological treatments is of fundamental importance especially for the most severe forms of MKD, in which even the nervous system is involved.
2. Generalities on Mevalonate Pathway in the Central Nervous System
2.1. Neuroinflammation and the Mevalonate Pathway
Neuroinflammation plays with its action a fundamental role in the central nervous system (CNS), but, at the same time, it could exert both beneficial and detrimental effects on the nervous tissue. Indeed, a low-level, quick-ending and restrained inflammatory process is thought be neuroprotective, whereas the presence of a chronic process of inflammation could lead to negative effects.
The CNS has been considered for a long time an “immune privileged” area [13,14], even if this concept is still unclear and being studied. This privileged status is anatomically achieved due to the presence of the blood-brain barrier (BBB). The BBB is formed essentially by endothelial cells of brain capillaries in tight contact with astrocytes and pericytes, of which duties comprise to maintain the chemical balance and homeostasis within the CNS, to limit the passage of antibodies and immune cells into the brain, and to connect the neuronal environment with the periphery, in terms of transportation of selected substances in and out of the brain [15,16]. Thus, any dysfunction or disorder of this fundamental structure may lead to several diseases .
From an immunological point of view, CNS is also considered “immune privileged” due to the relative absence of specific antigen presenting cells  and the production of neuronal-supporting and anti-inflammatory molecules, such as TGF-α and IL-10 [19,20].
However, as said before, the “immune privileged” status of CNS is nowadays an important matter of study, since neurodegeneration is one of the most intriguing and challenging pathological condition in modern society. Indeed, despite these features, neuroinflammation occurs in many pathologies linked to CNS, such as neurodegenerative diseases, trauma and infections, and involves during its course several cellular and molecular components of innate and adaptive immunity .
The BBB has been discovered to have the ability to change its own permeability to cellular traffic according to molecular signaling of local-secreted cytokines and chemokines . In addition, CNS hosts resident cells of innate immunity, microglia and astrocytes. Microglial cells represent the neuronal counter-part of macrophages, since they belong to the monocyte-macrophage system. They physiologically patrol and monitor the CNS in a quiescent state, exerting neuroprotective and neurogenetic actions, as well as homeostasis maintenance [23–25]. However, they have the capacity to be activated, proliferate, and assume an amoeboid shape when pathological changes occur [13,26]. Once activated, microglial cells gain macrophagic activity and upregulate MHC-II, absorbing debris and apoptotic cells and exposing antigens as antigen-presenting cells (APCs) . Furthermore, they start to secrete proinflammatory cytokines, such as TNF-α, IL-6 and IL-1β, and chemokines, such as RANTES and MCP-1, in order to recruit professional APCs to the site of damage . In physiological conditions, astrocytes are involved in the constitution of the BBB and serve as support to neurons, but they can also be activated in case of damage or inflammation and change their shape in order to generate a glial scar. As well as microglia, these cells are also able to release cytokines and chemokines, such as TNF-α, IL-6 and IL-1, and IFN-γ .
2.2. Cholesterol Metabolism in the Central Nervous System
Cholesterol metabolism at systemic levels is regulated by a fine balance between endogenous production, exogenous uptake, and, finally, by the exchange and transportation between several body districts mediated by apolipoproteins transported by the blood flow . However, due to the presence of the BBB, the CNS is isolated from the turnover of systemic cholesterol and develops an autonomous mechanism for the maintenance of biosynthesis and homeostasis of this molecule. In the CNS, neurons and glia tightly cooperate in order to achieve this aim. Even if every cell type is able to synthesize it, it has been demonstrated that astrocytes produce from two- to three-fold more cholesterol than neurons  and deliver it to neuronal cells via apolipoproteins (ApoE, ApoD, ApoJ, ApoA1) . The brain is the most cholesterol-rich region of the mammalian body, and this molecule is crucial to neurons, as it influences the synaptic function due its structural role in the synaptic membrane . For this reason a perturbation of this metabolic pathway often leads to a pathological condition. As previously mentioned, almost all brain cholesterol is produced in situ, and, in case of a blockade of the pathway, compensatory mechanisms (for example, dietary intake) are lacking. Indeed, it has been seen that the imbalance in the CNS cholesterol homeostasis is often concurrent to several neurodegenerative diseases, even if the underlying mechanisms have not been discovered yet. Thus, the reduction of cholesterol levels seems to affect the synaptic transmission. Indeed, an intrinsic blockade of the mevalonate pathway caused by a genetic mutation in the developing brain of a newborn, may affect the entire growth of a physiological neuronal network, as it actually seems to occur in the most severe cases of MKD.
3. Models of MKD: In Vitro and in Vivo
The search of new drugs/therapies for MKD could take advantage of in vitro and in vivo models mimicking the characteristics of the human disease.
For ethical reasons, rather than on a MKD animal model, researchers focused first on a cellular model.
Indeed, a MKD model has been developed to reproduce the genetic deregulation on the mevalonate pathway using compounds, such as aminobisphosphonates and/or statins, known to inhibit different enzymes of this biochemical pathway (Figure 1a). This system led to a moderate inflammatory phenotype that could be amplified by the subsequent administration of a bacterial compound, such as muramyl dipeptide (MDP) or lipopolysaccharide (LPS) [34,35]. The role of these pro-inflammatory agents was to mimic the acute phase of the inflammatory process.
The cellular lines chosen for this purpose were primarily monocytes and macrophagic cells, as researchers wanted to study the inhibitory effect in the component of the immune system, which was involved in the inflammation response shown by MKD patients.
Using the same biochemical approach and mechanism, a biochemical mouse model was developed , showing that the inhibition of the mevalonate pathway, through the use of aminobiphosphonates, leads to a moderate inflammatory phenotype that could be amplified by the subsequent injection of MDP or LPS [5,37].
One of the main limit of this approach is represented by the absence of a system able to measure intermediate compounds levels before and after treatments; moreover, data obtained using biochemical models are hardly comparable to those obtained using biological samples derived from MKD patients.
Even if the findings presented in these MKD models should be considered as preliminary, due to the adoption of a biochemical model of MKD, they should be taken as a first step in research aimed at better disclosing the MKD pathogenesis.
At present, a mouse model of MKD has been created with the deletion of one MVK , resulting in MKD phenocopy without the features of neurological dysfunction. Other reports on deletion of specific genes in cholesterol synthesis in the mouse model have revealed a high degree of embryonic lethality [39,40]. The lack of neurological involvement was the main weakness of this model, because it represents a crucial aspect of the most severe form of MKD disease.
It is important to say that cell lines from MKD patients do not exist: the anatomic evaluations of the neurological impairment of MKD patients have always been done and can be done only post-mortem. However, recently, a neuronal model of MKD has been developed in order to deepen the pathogenesis of this aspect of mevalonic aciduria .
4. Pathogenesis of Mevalonate Kinase Deficiency
While the excess of mevalonate is excreted via the kidneys in the urine, a shortage of downstream compounds is observed. Farnesyl pyrophosphate (FPP) is the branch point metabolite of the mevalonate pathway from which several biosynthetic routes depart. Of these pathways, one leads to squalene, cholesterol, and correlated metabolites, one leads to dolichol, polyprenyl chains of Heme A and ubiquinone, and one leads to geranylgeranyl pyrophosphate (GGPP) (Figure 1a).
In MKD patients not all these pathways are affected equally. Indeed, serum cholesterol remains within normal levels, as well as hepatic squalene and dolichol. On the contrary, a number of lowered metabolites of the mevalonate pathway are involved in protein prenylation.
Most proteins from the small GTPase superfamily are prenylated, and alterations in this post-translational mechanism could lead to altered localization or activation when isoprenoids are lacking [4,44].
It has been demonstrated that the lack of isoprenoids is associated with a decreased inflammation threshold, and conversely that exogenous isoprenoids can neutralize the pro-inflammatory phenotype both in ex vivo monocytes of MKD patients and in murine models [5,6]. A possible link between the lack of isoprenoids and inflammation could be explained by the overactivity of GTPases, which causes an activation of inflammasome and subsequently of caspase-1. Caspase-1 is required for the activation of IL-1β, maybe the most important pro-inflammatory cytokine in MKD.
Inflammasomes are cytoplasmic multi-protein complexes that function as sensors of endogenous or exogenous PAMPs (pathogen-associated molecular patterns). They are composed of one of several nucleotide-binding oligomerization-domain protein-like receptors (NLRs), including NLRP1, NLRP3, NLRP6, and NLRPC4. On sensing the relevant signal, they assemble, typically together with an adaptor protein, an apoptosis-associated speck-like protein (ASC) or a caspase activating and recruitment domain 8 (CARD8), into a multi-protein complex that governs caspase-1 activation and subsequent cleavage of effector pro-inflammatory cytokines, including pro-IL-1β and pro-IL-18. In addition, the function of mitochondria can be impaired, due to altered prenylation of Heme A and ubiquinone. Alteration in mitochondria function leads to release of ROS and other molecules capable to activate once more the inflammasome. Moreover, it has been recently demonstrated that mitochondrial ROS can activate NLRP3 and re-localize it to the mitochondrial membrane, through microtubule transport, where it is able to form a functional inflammasome with ASC and caspase-1 [10,45,46].
Activation of inflammasome with release of IL-1β causes attacks of fever in MKD patients, but, at a cellular level, it leads to an increase in cell death that resemble the mechanism of pyroptosis. IL-1β release is a complicated event, which is influenced by cell type and by the inflammatory stimulus. It has been demonstrated that activation of caspase-1 may need different stimuli to induce the activation of inflammasome in macrophages or glial cells, with regards to ATP-dependent mechanisms [47,48].
This could explain why pharmacological therapies can exert different degrees of control over the inflammation phenotype, while the neurological involvement, particularly severe in MA, remains the most important goal to be reached. Moreover, patients carrying same mutations on the MVK gene often exhibit a high variability of symptoms and, consequently, also of responses to the therapies. Although it is not established yet, this high variability could be explained by other genes or by the genetic background of patients, which contribute to the development of MKD.
5. Programmed Cell Death
5.1.1. Generalities on Apoptosis
Apoptosis is an active programmed cell death and is described as immunologically silent. It is characterized by activation of cysteinyl aspartate-specific proteases or caspases that are divided into caspase initiators and effectors, depending on their point of entry into the apoptotic pathway. The intrinsic apoptosis pathway, also known as mitochondrial pathway, is activated by the initiator caspase-9 and by the effector caspase-3 .
The intrinsic pathway is activated by various intracellular stress conditions including DNA damage, cytotoxic insult, oxidative stress, infection, and cellular homeostasis. These various stimuli act by inhibiting or activating particular anti- or pro-apoptotic Bcl-2 family members [51,52].
The Bcl-2-associated X protein (Bax) is a very important pro-apoptotic protein. During cell stress, the inhibition of Bax is relieved, thus, promoting its oligomerization and the formation of channels into the mitochondria, through which cytochrome c is released into the cytosol . Subsequently, cytochrome c binds to apoptotic protease-activating factor 1 (Apaf-1), forming the apoptosome that activates caspase-9 in an ATP-dependent manner. Active capase-9 cleaves and activates effector caspase-3. Caspase-3 then cleaves target proteins to trigger programmed apoptosis cell death characterized by cytoplasmic and nuclear condensation, DNA cleavage and by the development of the membrane-enclosed apoptotic bodies [52,54].
The Bax-induced channel formed into the mitochondria, known as the mitochondrial apoptosis-induced channel (MAC), besides allowing the release of cytochrome c, is important for: (a) the dissipation of the mitochondrial transmembrane potential (Δψm); (b) the release of other proteins into the cytosol, such as a second mitochondria-derived activator of caspase (SMAC), also known as DIABLO; and (c) the inhibition of the respiratory chain that cause the ROS overproduction (Figure 1b) [55–58]. All these processes of mitochondrial damage are also supported by the involvement of other Bcl-2 family members that modulate the existing mitochondrial permeability transition pore complex (PTPC) .
These mitochondrial dysfunctions represent a central causal factor in the pathogenesis of neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, and many others [8,59,60]. In recent years, researchers focused on the identification of compounds able to block the mitochondrial damage and, subsequently, neuronal death.
5.1.2. Apoptosis in Mevalonate Kinase Deficiency
Apoptosis, in particular via the mitochondrial pathway, plays a very important role in MKD.
At systemic level the cells, in particular monocytes, follow caspase-3 dependent apoptosis. This process was observed both in primary human monocytes from MKD and in biochemical MKD models obtained from monocyte cell lines [61,62].
In patients with severe forms of MKD, magnetic resonance imaging revealed progressive cerebellum atrophy that seems to be a direct consequence of neuronal apoptosis . This is confirmed in biochemical MKD models obtained in neuroblastoma cell lines treated with statin, one inhibitor of the mevalonate pathway. The block of the pathway causes an increased apoptosis sustained by the activation of caspase-3 and caspase-9, and a mitochondrial dysfunction that plays a crucial and important role in the pathogenesis of MKD [41,48]. On the contrary, Evelien J. Bodar et al., in 2007, observed that hereditary periodic fever syndromes are characterized by a defect in apoptosis regulation. In fact, they suggest that a defect in apoptosis regulation is the main trigger of the inflammatory response in these syndromes .
5.2.1. Generalities on Pyroptosis
Pyroptosis, also known as caspase-1 dependent programmed cell death, is another form of programmed cell death. Unlike apoptosis, pyroptosis is not immunologically silent, as it involves the release of inflammatory cytokines IL-1β and IL-18 [65,66].
Pyroptosis has been initially described in monocytes, macrophages and dendritic cells infected with a range of microbial pathogens. It has also been observed in non-macrophage cells after non-infective stimuli, such as damage-associated molecular pattern molecules [67,68].
The pyroptotic activation of caspase-1 may be due to a multiprotein platform known as the inflammasome . Another mechanism of caspase-1 activation requires the involvement of ASC pyroptosome, composed of oligomerized ASC (apoptosis-associated speck-like protein containing a CARD) dimers [69,70].
In both cases, active caspase-1 induces the formation of discretely sized ion-permeable pores in the plasma membrane . These pores act on mitochondrial membrane potential and plasma membrane integrity, causing a dissipation of cellular ionic gradient, producing an increase osmotic pressure, water influx, cell swelling, release of cytokines, and, ultimately, cell lysis [72,73].
Furthermore, active caspase-1 catalyzes the proteolytic maturation of pro-IL-1β and pro-IL-18 into, respectively, IL-1β and IL-18. These cytokines are powerful mediators of inflammation that stimulate the production of secondary cytokines (Figure 1c) .
The pyroptotic pathway is characterized by a mitochondrial dysfunction. In this case, the mitochondrial damage is not the central causal factor of cellular death, it is only its consequence.
The caspase-1 activation, and consecutive cell death, plays a predominant role in the immune and central nervous systems and, in the brain, caspase-1 may directly regulate neuronal cell death in response to diverse insults [74–76].
5.2.2. Pyroptosis in Mevalonate Kinase Deficiency
In literature, only few studies focus on the role of pyroptosis in MKD. However, the researchers substantially agree in suggesting pyroptosis as a fundamental step in inducing the inflammatory phenotype of MKD patients. Studies performed both on cell lines, in which the mevalonate pathway was biochemically blocked, and on MKD-patients-derived cells revealed a hyperproduction of IL-1β and IL-18, supposedly due to an overactive caspase-1 [8,35,77]. A hypothesis is that pyroptosis, triggered by the hyperactivity of caspase-1, may be caused by the lack of isoprenoid compounds, intermediates of the mevalonate pathway.
IL-1 family and the mechanisms that lead to its activation, such as caspase-1 and inflammasomes, are crucial events even in neuronal damage. Several studies show how inflammatory processes occur after acute brain insults, as well as in chronic neurodegenerative diseases [78,79]. For this reason, some researchers suggest that the neuronal death seen in the most severe form of MKD may indeed be caused by pyroptosis, in addition to apoptosis .
6. Oxidative Stress and Mitochondrial Damage through the Mevalonate Pathway
Oxidative stress is characterized by the increase in reactive species and it is involved in the development of many degenerative diseases. Reactive oxygen species (ROS) are the most representative reactive species in the cells, and they mainly are originated by mitochondrial respiration. ROS have been implicated in many inflammatory diseases; in particular, Familial Mediterranean fevers are characterized by an increase of mitochondrial ROS [79–81].
When ROS are highly concentrated, they react with protein, lipid, nucleic acid and carbohydrates inducing irreversible alterations. ROS appear to play a role in activating NLRP3 inflammasome, which in turn activates caspase-1 and pro-inflammatory cytokines . ROS overproduction is a consequence of mitochondrial dysfunction related to apoptosis, and in particular to neuronal apoptosis.
In neurons, mitochondria participate in a variety of processes and play an essential role for providing energy and calcium buffering, required for synaptic transmission. In fact, mitochondrial damage is a central causal factor in the pathogenesis of neuroinflammation and neurodegeneration.
Mitochondrial dysfunction could be the link between neuroinflammation and neuronal degeneration. Dissipation of the mitochondrial transmembrane potential, the base of mitochondrial damage, is the most accredited cause of NALP3-inflammasome activation and subsequently release of pro-inflammatory cytokines. Similarly, this mitochondrial damage is the primary fundamental event of neuronal-programmed cell death.
Mevalonate pathway is important for the production of antioxidant molecules such as ubiquinone, heme A, selenoproteins and glutathione peroxidase.
Ubiquinone and heme A are involved in electron transport. Selenoproteins are important in development, metabolic homeostasis, and antioxidant defense. Glutathione peroxidase plays an important role in redox balance [82,83].
The block of the cholesterol pathway in MKD causes a shortage of these metabolites. In fact, a recent hypothesis is that the pathogenesis of MKD might be mainly explained by the oxidative stress related to the decrease of antioxidant molecules .
7. Concluding Remarks
Programmed cell death plays a crucial role in the inflammatory phenotype of MKD pathogenesis, and it has been demonstrated both in vitro and in animal models. Both apoptosis and pyroptosis are involved in the pathogenetic mechanism that sustains the secretion of IL-1β, the major marker of MKD, although, at present, the link between PCD and cytokines secretion remains unclear and PCD was evaluated both at system and cerebral levels in MKD models.
Moreover, recently published data have shown that the oxidative stress and mitochondrial damage act as a final trigger for PCD.
These new insights open a new frontier in the research of a pharmacological treatment for this orphan disease, by identifying new specific molecular targets, particularly for the treatment of its neurological aspects.
In conclusion, great improvements have been obtained in recent years in the field of MKD thanks to the identification of the molecular mechanisms involved in the pathogenesis of the disease, and in particular of the role of the PCD.
Although further studies are necessary, in our opinion a possible future application of these new findings could be the development of therapeutic strategies that will target the mitochondrial mechanism involved in MKD pathogenesis.
Tricarico P.M., Marcuzzi A. and Kleiner G. conceived the article structure; Marcuzzi A. and Crovella S. wrote the introduction and the inflammasome parts; Piscianz E. wrote the pathogenetic and PCD parts; Kleiner G. and Monasta L. wrote the neuroinflammation and the MKD models parts; Tricarico P.M. wrote the apoptosis and pyroptosis parts and the conclusions; Tricarico P.M., Kleiner G., Crovella S. and Marcuzzi A. assembled the manuscript; Monasta L. edited the final version of the manuscript.
Conflicts of Interest
The authors declare no conflict of interest.
- Goldstein, J.L.; Brown, M.S. Regulation of the mevalonate pathway. Nature 1990, 343, 425–430.
- Haas, D.; Hoffmann, G.F. Mevalonate kinase deficiency and autoinflammatory disorders. N. Engl. J. Med 2007, 356, 2671–2673.
- Drenth, J.P.; Haagsma, C.J.; van der Meer, J.W. Hyperimmunoglobulinemia D and periodic fever syndrome. The clinical spectrum in a series of 50 patients. International Hyper-IgD Study Group. Medicine 1994, 73, 133–144.
- Mandey, S.H.; Kuijk, L.M.; Frenkel, J.; Waterham, H.R. A role for geranylgeranylation in interleukin-1beta secretion. Arthritis Rheum 2006, 54, 3690–3695.
- Marcuzzi, A.; Pontillo, A.; de Leo, L.; Tommasini, A.; Decorti, G.; Not, T.; Ventura, A. Natural isoprenoids are able to reduce inflammation in a mouse model of mevalonate kinase deficiency. Pediatr. Res 2008, 64, 177–182.
- Frenkel, J.; Rijkers, G.T.; Mandey, S.H.; Buurman, S.W.; Houten, S.M.; Wanders, R.J.; Waterham, H.R.; Kuis, W. Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 2002, 46, 2794–2803.
- Marcuzzi, A.; de Leo, L.; Decorti, G.; Crovella, S.; Tommasini, A.; Pontillo, A. The farnesyltransferase inhibitors tipifarnib and lonafarnib inhibit cytokines secretion in a cellular model of mevalonate kinase deficiency. Pediatr. Res 2011, 70, 78–82.
- Marcuzzi, A.; Piscianz, E.; Girardelli, M.; Crovella, S.; Pontillo, A. Defect in mevalonate pathway induces pyroptosis in Raw 264.7 murine monocytes. Apoptosis 2011, 16, 882–888.
- Pontillo, A.; Paoluzzi, E.; Crovella, S. The inhibition of mevalonate pathway induces upregulation of NALP3 expression: New insight in the pathogenesis of mevalonate kinase deficiency. Eur. J. Hum. Genet 2010, 18, 844–847.
- Zhou, R.; Yazdi, A.S.; Menu, P.; Tschopp, J. A role for mitochondria in NLRP3 inflammasome activation. Nature 2011, 469, 221–225.
- Rubartelli, A.; Gattorno, M.; Netea, M.G.; Dinarello, C.A. Interplay between redox status and inflammasome activation. Trends Immunol 2011, 32, 559–566.
- Shimada, K.; Crother, T.R.; Karlin, J.; Dagvadorj, J.; Chiba, N.; Chen, S.; Ramanujan, V.K.; Wolf, A.J.; Vergnes, L.; Ojcius, D.M.; et al. Oxidized mitochondrial DNA activates the NLRP3 inflammasome during apoptosis. Immunity 2012, 36, 401–414.
- Cappellano, G.; Carecchio, M.; Fleetwood, T.; Magistrelli, L.; Cantello, R.; Dianzani, U.; Comi, C. Immunity and inflammation in neurodegenerative diseases. Am. J. Neurodegener. Dis 2013, 2, 89–107.
- Amor, S.; Puentes, F.; Baker, D.; van der Valk, P. Inflammation in neurodegenerative diseases. Immunology 2010, 129, 154–169.
- Abbott, N.J.; Patabendige, A.A.; Dolman, D.E.; Yusof, S.R.; Begley, D.J. Structure and function of the blood-brain barrier. Neurobiol. Dis 2010, 37, 13–25.
- Ransohoff, R.M.; Brown, M.A. Innate immunity in the central nervous system. J. Clin. Investig 2012, 122, 1164–1171.
- Erickson, M.A.; Banks, W.A. Blood-brain barrier dysfunction as a cause and consequence of Alzheimer’s disease. J. Cereb. Blood Flow Metab 2013, 33, 1500–1513.
- Galea, I.; Bechmann, I.; Perry, V.H. What is immune privilege (not)? Trends Immunol 2007, 28, 12–18.
- Dobolyi, A.; Vincze, C.; Pál, G.; Lovas, G. The neuroprotective functions of transforming growth factor beta proteins. Int. J. Mol. Sci 2012, 13, 8219–8258.
- Strle, K.; Zhou, J.H.; Shen, W.H.; Broussard, S.R.; Johnson, R.W.; Freund, G.G.; Dantzer, R.; Kelley, K.W. Interleukin-10 in the brain. Crit. Rev. Immunol 2001, 21, 427–449.
- Rubio-Perez, J.M.; Morillas-Ruiz, J.M. A review: Inflammatory process in Alzheimer’s disease, role of cytokines. Sci. World J 2012, 2012, 756357.
- Owens, T.; Bechmann, I.; Engelhardt, B. Perivascular spaces and the two steps to neuroinflammation. J. Neuropathol. Exp. Neurol 2008, 67, 1113–1121.
- Olah, M.; Amor, S.; Brouwer, N.; Vinet, J.; Eggen, B.; Biber, K.; Boddeke, H.W. Identification of a microglia phenotype supportive of remyelination. Glia 2012, 60, 306–321.
- Sierra, A.; Encinas, J.M.; Deudero, J.J.; Chancey, J.H.; Enikolopov, G.; Overstreet-Wadiche, L.S.; Tsirka, S.E.; Maletic-Savatic, M. Microglia shape adult hippocampal neurogenesis through apoptosis-coupled phagocytosis. Cell Stem Cell 2010, 7, 483–495.
- Vinet, J.; Weering, H.R.; Heinrich, A.; Kälin, R.E.; Wegner, A.; Brouwer, N.; Heppner, F.L.; Rooijen, N.; Boddeke, H.W.; Biber, K. Neuroprotective function for ramified microglia in hippocampal excitotoxicity. J. Neuroinflamm 2012, 9, 27.
- Shastri, A.; Bonifati, D.M.; Kishore, U. Innate immunity and neuroinflammation. Mediat. Inflamm 2013, doi:10.1155/2013/342931.
- Kreutzberg, G.W. Microglia: A sensor for pathological events in the CNS. Trends Neurosci 1996, 19, 312–318.
- Olson, J.K.; Miller, S.D. Microglia initiate central nervous system innate and adaptive immune responses through multiple TLRs. J. Immunol 2004, 173, 3916–3924.
- Sofroniew, M.V.; Vinters, H.V. Astrocytes: Biology and pathology. Acta Neuropathol 2010, 119, 7–35.
- Pfrieger, F.W.; Ungerer, N. Cholesterol metabolism in neurons and astrocytes. Prog. Lipid Res 2011, 50, 357–371.
- Saito, M.; Benson, E.P.; Saito, M.; Rosenberg, A. Metabolism of cholesterol and triacylglycerol in cultured chick neuronal cells, glial cells, and fibroblasts: Accumulation of esterified cholesterol in serum-free culture. J. Neurosci. Res 1987, 18, 319–325.
- Pitas, R.E.; Boyles, J.K.; Lee, S.H.; Hui, D.; Weisgraber, K.H. Lipoproteins and their receptors in the central nervous system. Characterization of the lipoproteins in cerebrospinal fluid and identification of apolipoprotein B,E (LDL) receptors in the brain. J. Biol. Chem 1987, 262, 14352–14360.
- Mailman, T.; Hariharan, M.; Karten, B. Inhibition of neuronal cholesterol biosynthesis with lovastatin leads to impaired synaptic vesicle release even in the presence of lipoproteins or. geranylgeraniol. J. Neurochem 2011, 119, 1002–10015.
- Marcuzzi, A.; Tommasini, A.; Crovella, S.; Pontillo, A. Natural isoprenoids inhibit LPS-induced-production of cytokines and nitric oxide in aminobisphosphonate-treated monocytes. Int. Immunopharmacol 2010, 10, 639–642.
- Kuijk, L.M.; Mandey, S.H.; Schellens, I.; Waterham, H.R.; Rijkers, G.T.; Coffer, P.J.; Frenkel, J. Statin synergizes with LPS to induce IL-1beta release by THP-1 cells through activation of caspase-1. Mol. Immunol 2008, 45, 2158–2165.
- Yu, Z.; Funayama, H.; Deng, X.; Kuroishi, T.; Sasano, T.; Sugawara, S.; Endo, Y. Comparative appraisal of clodronate, aspirin and dexamethasone as agents reducing alendronate-induced inflammation in a murine model. Basic Clin. Pharmacol. Toxicol 2005, 97, 222–229.
- Marcuzzi, A.; Crovella, S.; Monasta, L.; Vecchi Brumatti, L.; Gattorno, M.; Frenkel, J. Mevalonate kinase deficiency: Disclosing the role of mevalonate pathway modulation in inflammation. Curr. Pharm. Des 2012, 18, 5746–5752.
- Hager, E.J.; Tse, H.M.; Piganelli, J.D.; Gupta, M.; Baetscher, M.; Tse, T.E.; Pappu, A.S.; Steiner, R.D.; Hoffmann, G.F.; Gibson, K.M. Deletion of a single mevalonate kinase (Mvk) allele yields a murine model of hyper-IgD syndrome. J. Inherit. Metab. Dis 2007, 30, 888–895.
- Ohashi, K.; Osuga, J.; Tozawa, R.; Kitamine, T.; Yagyu, H.; Sekiya, M.; Tomita, S.; Okazaki, H.; Tamura, Y.; Yahagi, N.; et al. Early embryonic lethality caused by targeted disruption of the 3-hydroxy-3-methylglutaryl-CoA reductase gene. J. Biol. Chem 2003, 278, 42936–42941.
- Tozawa, R.; Ishibashi, S.; Osuga, J.; Yagyu, H.; Oka, T.; Chen, Z.; Ohashi, K.; Perrey, S.; Shionoiri, F.; Yahagi, N.; et al. Embryonic lethality and defective neural tube closure in mice lacking squalene synthase. J. Biol. Chem 1999, 274, 30843–30848.
- Marcuzzi, A.; Tricarico, P.M.; Piscianz, E.; Kleiner, G.; Brumatti, L.V.; Crovella, S. Lovastatin induces apoptosis through the mitochondrial pathway in an undifferentiated SH-SY5Y neuroblastoma cell line. Cell Death Dis 2013, 4, e585.
- Van der Burgh, R.; Ter Haar, N.M.; Boes, M.L.; Frenkel, J. Mevalonate kinase deficiency, a metabolic autoinflammatory disease. Clin. Immunol 2013, 147, 197–206.
- Brough, D.; Rothwell, N.J. Caspase-1-dependent processing of pro-interleukin-1beta is cytosolic and precedes cell death. J. Cell. Sci 2007, 120, 772–781.
- Henneman, L.; Schneiders, M.S.; Turkenburg, M.; Waterham, H.R. Compromized geranylgeranylation of RhoA and Rac1 in mevalonate kinase deficiency. J. Inherit. Metab. Dis 2010, 33, 625–632.
- Misawa, T.; Takahama, M.; Kozaki, T.; Lee, H.; Zou, J.; Saitoh, T.; Akira, S. Microtubule-driven spatial arrangement of mitochondria promotes activation of the NLRP3 inflammasome. Nat. Immunol 2013, 14, 454–460.
- Lawlor, K.E.; Vince, J.E. Ambiguities in NLRP3 inflammasome regulation: Is there a role for mitochondria? Biochim. Biophys. Acta 2013. in press.
- Liao, Y.H.; Lin, Y.C.; Tsao, S.T.; Lin, Y.C.; Yang, A.J.; Huang, C.T.; Huang, K.C.; Lin, W.W. HMG-CoA reductase inhibitors activate caspase-1 in human monocytes depending on ATP release and P2X7 activation. J. Leukoc. Biol 2013, 93, 289–299.
- Gattorno, M.; Tassi, S.; Carta, S.; Delfino, L.; Ferlito, F.; Pelagatti, M.A.; D’Osualdo, A.; Buoncompagni, A.; Alpigiani, M.G.; Alessio, M.; et al. Pattern of interleukin-1beta secretion in response to lipopolysaccharide and ATP before and after interleukin-1 blockade in patients with CIAS1 mutations. Arthritis Rheum 2007, 56, 3138–3148.
- Marcuzzi, A.; Zanin, V.; Piscianz, E.; Tricarico, P.M.; Vuch, J.; Girardelli, M.; Monasta, L.; Bianco, A.M.; Crovella, S. Lovastatin-induced apoptosis is modulated by geranylgeraniol in a neuroblastoma cell line. Int. J. Dev. Neurosci 2012, 30, 451–456.
- Fuentes-Prior, P.; Salvesen, G.S. The protein structures that shape caspase activity, specificity, activation and inhibition. Biochem. J 2004, 384, 201–232.
- Galluzzi, L.; Vitale, I.; Abrams, J.M.; Alnemri, E.S.; Baehrecke, E.H.; Blagosklonny, M.V.; Dawson, T.M.; Dawson, V.L.; El-Deiry, W.S.; Fulda, S.; et al. Molecular definitions of cell death subroutines: Recommendations of the Nomenclature Committee on Cell Death 2012. Cell Death Differ 2012, 19, 107–120.
- Herrero-Martin, G.; López-Rivas, A. Statins activate a mitochondria-operated pathway of apoptosis in breast tumor cells by a mechanism regulated by ErbB2 and dependent on the prenylation of proteins. FEBS Lett 2008, 582, 2589–2594.
- Long, A.B.; Kaiser, W.J.; Mocarski, E.S.; Caspary, T. Apaf1 apoptotic function critically limits Sonic hedgehog signaling during craniofacial development. Cell Death Differ 2013, 20, 1510–1520.
- Martinez-Caballero, S.; Dejean, L.M.; Kinnally, M.S.; Oh, K.J.; Mannella, C.A.; Kinnally, K.W. Assembly of the mitochondrial apoptosis-induced channel, MAC. J. Biol. Chem 2009, 284, 12235–12245.
- Kroemer, G.; Galluzzi, L.; Brenner, C. Mitochondrial membrane permeabilization in cell death. Physiol. Rev 2007, 87, 99–163.
- Ng, H.; Smith, D.J.; Nagley, P. Application of flow cytometry to determine differential redistribution of cytochrome c and Smac/DIABLO from mitochondria during cell death signaling. PLoS One 2012, 7, e42298.
- Simon, H.U.; Haj-Yehia, A.; Levi-Schaffer, F. Role of reactive oxygen species (ROS) in apoptosis induction. Apoptosis 2000, 5, 415–418.
- Schinzel, A.C.; Takeuchi, O.; Huang, Z.; Fisher, J.K.; Zhou, Z.; Rubens, J.; Hetz, C.; Danial, N.N.; Moskowitz, M.A.; Korsmeyer, S.J. Cyclophilin D is a component of mitochondrial permeability transition and mediates neuronal cell death after focal cerebral ischemia. Proc. Natl. Acad. Sci. USA 2005, 102, 12005–12010.
- García-Escudero, V.; Martín-Maestro, P.; Perry, G.; Avila, J. Deconstructing mitochondrial dysfunction in Alzheimer disease. Oxid. Med. Cell. Longev 2013, doi:10.1155/2013/162152.
- Hauser, D.N.; Hastings, T.G. Mitochondrial dysfunction and oxidative stress in Parkinson’s disease and monogenic parkinsonism. Neurobiol. Dis 2013, 51, 35–42.
- Johri, A.; Beal, M.F. Mitochondrial dysfunction in neurodegenerative diseases. J. Pharmacol. Exp. Ther 2012, 342, 619–630.
- Tricarico, P.M.; Kleiner, G.; Piscianz, E.; Zanin, V.; Monasta, L.; Crovella, S.; Marcuzzi, A. Temperature and drug treatments in mevalonate kinase deficiency: An ex vivo study. BioMed Res. Int 2013, 2013, 8.
- Ruiz Gomez, A.; Couce, M.L.; Garcia-Villoria, J.; Torres, A.; Baña Souto, A.; Yagüe, J.; Vilaseca, M.A.; Ribes, A.; Aróstegui, J.I. Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency. Pediatrics 2012, 129, 535–539.
- Bodar, E.J.; van der Hilst, J.C.; van Heerde, W.; van der Meer, J.W.; Drenth, J.P.; Simon, A. Defective apoptosis of peripheral-blood lymphocytes in hyper-IgD and periodic fever syndrome. Blood 2007, 109, 2416–2418.
- Fantuzzi, G.; Dinarello, C.A. Interleukin-18 and interleukin-1 beta: Two cytokine substrates for ICE (caspase-1). J. Clin. Immunol 1999, 19, 1–11.
- Bergsbaken, T.; Fink, S.L.; Cookson, B.T. Pyroptosis: Host cell death and inflammation. Nat. Rev. Microbiol 2009, 7, 99–109.
- Denes, A.; Lopez-Castejon, G.; Brough, D. Caspase-1: Is IL-1 just the tip of the ICEberg? Cell Death Dis 2012, 3, e338.
- Byrne, B.G.; Dubuisson, J.F.; Joshi, A.D.; Persson, J.J.; Swanson, M.S. Inflammasome components coordinate autophagy and pyroptosis as macrophage responses to infection. MBio 2013, 4, doi:10.1128/mBio.00620-12.
- Fernandes-Alnemri, T.; Wu, J.; Yu, J.W.; Datta, P.; Miller, B.; Jankowski, W.; Rosenberg, S.; Zhang, J.; Alnemri, E.S. The pyroptosome: A supramolecular assembly of ASC dimers mediating inflammatory cell death via caspase-1 activation. Cell Death Differ 2007, 14, 1590–1604.
- Fink, S.L.; Cookson, B.T. Caspase-1-dependent pore formation during pyroptosis leads to osmotic lysis of infected host macrophages. Cell Microbiol 2006, 8, 1812–1825.
- Case, C.L. Regulating caspase-1 during infection: Roles of NLRs, AIM2, and ASC. Yale J. Biol. Med 2011, 84, 333–343.
- Miao, E.A.; Leaf, I.A.; Treuting, P.M.; Mao, D.P.; Dors, M.; Sarkar, A.; Warren, S.E.; Wewers, M.D.; Aderem, A. Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria. Nat. Immunol 2010, 11, 1136–1142.
- Suzuki, H.; Sozen, T.; Hasegawa, Y.; Chen, W.; Zhang, J.H. Caspase-1 inhibitor prevents neurogenic pulmonary edema after subarachnoid hemorrhage in mice. Stroke 2009, 40, 3872–3875.
- Loda, E.; Balabanov, R. Interferon regulatory factor 1 regulation of oligodendrocyte injury and inflammatory demyelination. Rev. Neurosci 2012, 23, 145–152.
- Allan, S.M.; Tyrrell, P.J.; Rothwell, N.J. Interleukin-1 and neuronal injury. Nat. Rev. Immunol 2005, 5, 629–640.
- Normand, S.; Massonnet, B.; Delwail, A.; Favot, L.; Cuisset, L.; Grateau, G.; Morel, F.; Silvain, C.; Lecron, J.C. Specific increase in caspase-1 activity and secretion of IL-1 family cytokines: A putative link between mevalonate kinase deficiency and inflammation. Eur. Cytokine Netw 2009, 20, 101–107.
- Brough, D.; Tyrrell, P.J.; Allan, S.M. Regulation of interleukin-1 in acute brain injury. Trends Pharmacol. Sci 2011, 32, 617–622.
- Simi, A.; Tsakiri, N.; Wang, P.; Rothwell, N.J. Interleukin-1 and inflammatory neurodegeneration. Biochem. Soc. Trans 2007, 35, 1122–1126.
- Bulua, A.C.; Simon, A.; Maddipati, R.; Pelletier, M.; Park, H.; Kim, K.Y.; Sack, M.N.; Kastner, D.L.; Siegel, R.M. Mitochondrial reactive oxygen species promote production of proinflammatory cytokines and are elevated in TNFR1-associated periodic syndrome (TRAPS). J. Exp. Med 2011, 208, 519–533.
- Moosmann, B.; Behl, C. Selenoproteins, cholesterol-lowering drugs, and the consequences: Revisiting of the mevalonate pathway. Trends Cardiovasc. Med 2004, 14, 273–281.
- Omenetti, A.; Carta, S.; Delfino, L.; Martini, A.; Gattorno, M.; Rubartelli, A. Increased NLRP3-dependent interleukin 1β secretion in patients with familial Mediterranean fever: Correlation with MEFV genotype. Ann. Rheum. Dis 2013. in press.
- Rodríguez-Martínez, E.; Martínez, F.; Espinosa-García, M.T.; Maldonado, P.; Rivas-Arancibia, S. Mitochondrial dysfunction in the hippocampus of rats caused by chronic oxidative stress. Neuroscience 2013, 252, 384–395.
- Celec, P.; Behuliak, M. The lack of non-steroid isoprenoids causes oxidative stress in patients with mevalonic aciduria. Med. Hypotheses 2008, 70, 938–940.
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