Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: Mechanistic relationship and differential sensitivity to intervention
Tài liệu tham khảo
Alexianu, 1994, The role of calcium-binding proteins in selective motoneuron vulnerability in amyotrophic lateral sclerosis, Ann. Neurol., 6846
Arber, 1999, Requirement for the homeobox gene Hb9 in the consolidation of motor neuron identity, Neuron, 4659
Arribas, 1990, Kinetic studies of the differential effect of detergents on the peptidase activities of the multicatalytic proteinase from rat liver, J. Biol. Chem., 2313969
Batulan, 2006, Induction of multiple heat shock proteins and neuroprotection in a primary culture model of familial amyotrophic lateral sclerosis, Neurobiol. Dis., 2213
Beers, 2001, Parvalbumin overexpression alters immune-mediated increases in intracellular calcium, and delays disease onset in a transgenic model of familial amyotrophic lateral sclerosis, J. Neurochem., 3499
Bence, 2001, Impairment of the ubiquitin-proteasome system by protein aggregation, Science, 55211552
Bendotti, 2001, Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity, J. Neurol. Sci., 1-225-33
Bennett, 2005, Global impairment of the ubiquitin-proteasome system by nuclear or cytoplasmic protein aggregates precedes inclusion body formation, Mol. Cell, 3351
Bergemalm, 2006, Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis models, J. Neurosci., 164147
Bilsland, 2008, Expression of mutant SOD1 in astrocytes induces functional deficits in motoneuron mitochondria, J. Neurochem., 51271
Boerio, 2010, Excitability properties of mouse motor axons in the mutant SOD1(G93A) model of amyotrophic lateral sclerosis, Muscle Nerve, 41, 6774, 10.1002/mus.21579
Borthwick, 1999, Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death, Ann Neurol., 46, 787, 10.1002/1531-8249(199911)46:5<787::AID-ANA17>3.0.CO;2-8
Breckenridge, 2003, Caspase cleavage product of BAP31 induces mitochondrial fission through endoplasmic reticulum calcium signals, enhancing cytochrome c release to the cytosol, J. Cell Biol., 71115
Bruening, 1999, Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis, J. Neurochem., 2693
Bruijn, 1997, ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions, Neuron, 2327
Buckman, 2001, Spontaneous changes in mitochondrial membrane potential in cultured neurons, J. Neurosci., 145054
Carri, 1997, Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells, FEBS Lett., 2365
Carriedo, 2000, AMPA exposures induce mitochondrial Ca(2+) overload and ROS generation in spinal motor neurons in vitro, J. Neurosci., 1240
Chen, 2003, Rapid Ca2+-dependent decrease of protein ubiquitination at synapses, Proc. Natl Acad. Sci. USA, 2514908
Cobbold, 1987, Fluorescence and bioluminescence measurement of cytoplasmic free calcium, Biochem. J., 2313
Cozzolino, 2008, Amyotrophic lateral sclerosis: from current developments in the laboratory to clinical implications, Antioxid. Redox. Signal., 3405
Dal Canto, 1994, Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis, Am. J. Pathol., 61271
Damiano, 2006, Neural mitochondrial Ca2+ capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn-superoxide dismutase mutant mice, J. Neurochem., 51349
Djakovic, 2009, Regulation of the proteasome by neuronal activity and calcium/calmodulin-dependent protein kinase II, J. Biol. Chem., 3926655
Durham, 1992, An antibody against hyperphosphorylated neurofilament proteins collapses the neurofilament network in motor neurons but not in dorsal root ganglion cells, J. Neuropathol. Exp. Neurol., 3287
Durham, 1997, Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS, J. Neuropathol. Exp. Neurol., 5523
Geisler, 2010, PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1, Nat Cell Biol., 2119
Gingras, 2007, Optimized protocols for isolation of primary motor neurons, astrocytes and microglia from embryonic mouse spinal cord, J. Neurosci. Methods., 1111
Grosskreutz, 2007, Role of mitochondria in kainate-induced fast Ca2+ transients in cultured spinal motor neurons, Cell Calcium, 42, 159, 10.1016/j.ceca.2006.11.010
Higgins, 2003, ALS-associated mutant SOD1G93A causes mitochondrial vacuolation by expansion of the intermembrane space and by involvement of SOD1 aggregation and peroxisomes, BMC Neurosci., 4, 16, 10.1186/1471-2202-4-16
Ince, 1993, Parvalbumin and calbindin D-28k in the human motor system and in motor neuron disease, Neuropathol. Appl. Neurobiol., 4291
Jaarsma, 2001, CuZn superoxide dismutase (SOD1) accumulates in vacuolated mitochondria in transgenic mice expressing amyotrophic lateral sclerosis-linked SOD1 mutations, Acta Neuropathol., 102, 4293, 10.1007/s004010100399
Jahn, 2006, Temporospatial coupling of networked synaptic activation of AMPA-type glutamate receptor channels and calcium transients in cultured motoneurons, Neuroscience, 142, 41019, 10.1016/j.neuroscience.2006.07.034
Jaiswal, 2009, Cu/Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of mitochondria and perturbs Ca2+ homeostasis in SOD1G93A mice, Mol. Pharmacol., 3478
Kabashi, 2004, Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis., J. Neurochem., 89, 61325, 10.1111/j.1471-4159.2004.02453.x
Kanai, 2006, Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage, Brain, Pt 4953
Kanekura, 2009, ER stress and unfolded protein response in amyotrophic lateral sclerosis, Mol. Neurobiol., 39, 281, 10.1007/s12035-009-8054-3
Kann, 2007, Mitochondria and neuronal activity, Am. J. Physiol. Cell Physiol., 2C641
Kawamata, 2010, Mitochondrial dysfunction and intracellular calcium dysregulation in ALS, Mech. Ageing Dev., 131, 517, 10.1016/j.mad.2010.05.003
Kieran, 2004, Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice, Nat. Med., 4402
Kim, 2007, Calcium-influx increases SOD1 aggregates via nitric oxide in cultured motor neurons, Exp. Mol. Med., 5574
Kirichok, 2004, The mitochondrial calcium uniporter is highly selective ion channel, Nature, 427, 6972360, 10.1038/nature02246
Kirkinezos, 2005, Cytochrome c association with the inner mitochondrial membrane is impaired in the CNS of G93A-SOD1 mice, J. Neurosci., 1164
Knott, 2008, Mitochondrial fragmentation in neurodegeneration, Nat. Rev. Neurosci., 7505
Kong, 1998, Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1, J. Neurosci., 18, 93241, 10.1523/JNEUROSCI.18-09-03241.1998
Kopito, 2000, Aggresomes, inclusion bodies and protein aggregation, Trends Cell Biol., 12524
Kruman, 1999, ALS-linked Cu/Zn-SOD mutation increases vulnerability of motor neurons to excitotoxicity by a mechanism involving increased oxidative stress and perturbed calcium homeostasis, Exp. Neurol., 128
Kuner, 2005, Mechanisms of disease: motoneuron disease aggravated by transgenic expression of a functionally modified AMPA receptor subunit, Ann. NY Acad. Sci., 269, 10.1196/annals.1344.024
Landowski, 2005, Mitochondrial-mediated disregulation of Ca2+ is a critical determinant of Velcade (PS-341/bortezomib) cytotoxicity in myeloma cell lines, Cancer Res., 93828
Liu, 2004, Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria, Neuron, 15
Martin, 2007, Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: mechanisms of mitochondriopathy and cell death, J. Comp. Neurol., 120
Nagai, 2001, Circularly permuted green fluorescent proteins engineered to sense Ca2+, Proc. Natl Acad. Sci. USA, 63197
Nawrocki, 2008, Myc regulates aggresome formation, the induction of Noxa, and apoptosis in response to the combination of bortezomib and SAHA, Blood, 72917
Nguyen, 2009, The Psi(m) depolarization that accompanies mitochondrial Ca2+ uptake is greater in mutant SOD1 than in wild-type mouse motor terminals, Proc. Natl Acad. Sci. USA, 62007
Palmer, 2004, Bcl-2-mediated alterations in endoplasmic reticulum Ca2+ analyzed with an improved genetically encoded fluorescent sensor, Proc. Natl Acad. Sci. USA, 5017404
Pambo-Pambo, 2009, Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice, J. Neurophysiol., 63627
Pasinelli, 2004, Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria, Neuron, 119
Pedrini, 2010, ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2, Hum. Mol. Genet., 152974
Perry, 1990, Amyotrophic lateral sclerosis: amino acid levels in plasma and cerebrospinal fluid, Ann. Neurol., 112
Realini, 1995, A proteasome activator subunit binds calcium, J. Biol. Chem., 270, 5029664, 10.1074/jbc.270.50.29664
Rock, 1994, Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules, Cell, 5761
Rosen, 1993, Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis, Nature, 641559
Rothstein, 1990, Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis, Ann. Neurol., 118
Roy, 1998, Glutamate potentiates the toxicity of mutant Cu/Zn-superoxide dismutase in motor neurons by postsynaptic calcium-dependent mechanisms, J. Neurosci., 18, 239673, 10.1523/JNEUROSCI.18-23-09673.1998
Rustenbeck, 1993, Effect of spermine on mitochondrial matrix calcium in relation to its enhancement of mitochondrial calcium uptake, Biochem. Biophys. Res. Commun., 194, 31261, 10.1006/bbrc.1993.1959
Sasaki, 2007, Mitochondrial alterations in dorsal root ganglion cells in sporadic amyotrophic lateral sclerosis, Acta Neuropathol., 114, 6633, 10.1007/s00401-007-0299-1
Sasaki, 1996, Ultrastructural study of synapses in the anterior horn neurons of patients with amyotrophic lateral sclerosis, Neurosci. Lett., 1-253-6
Shaw, 2007, How do ALS-associated mutations in superoxide dismutase 1 promote aggregation of the protein?, Trends Biochem. Sci., 278
Shimozono, 2002, Confocal imaging of subcellular Ca2+ concentrations using a dual-excitation ratiometric indicator based on green fluorescent protein, Sci. STKE, 125L4
Siklos, 1996, Ultrastruct. evidence altered calcium motor nerve terminals amyotropic lateral sclerosis, Ann. Neurol., 39, 2203, 10.1002/ana.410390210
Siklos, 1998, Intracellular calcium parallels motoneuron degeneration in SOD-1 mutant mice, J. Neuropathol. Exp. Neurol., 6571
Son, 2007, Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology, Proc. Natl Acad. Sci. USA, 146072
Sullivan, 2004, Proteasome inhibition alters neural mitochondrial homeostasis and mitochondria turnover, J. Biol. Chem., 2020699
Swerdlow, 1998, Mitochondria in sporadic amyotrophic lateral sclerosis, Exp Neurol., 153, 135, 10.1006/exnr.1998.6866
Tai, 2010, Characterization of the brain 26S proteasome and its interacting proteins, Front. Mol. Neurosci., 20101
Tateno, 2004, Calcium-permeable AMPA receptors promote misfolding of mutant SOD1 protein and development of amyotrophic lateral sclerosis in a transgenic mouse model, Hum. Mol. Genet., 192183
Taylor, 2004, Overexpression of metallothionein protects cultured motor neurons against oxidative stress, but not mutant Cu/Zn-superoxide dismutase toxicity, Neurotoxicology, 5779
Tortarolo, 2006, Glutamate AMPA receptors change in motor neurons of SOD1G93A transgenic mice and their inhibition by a noncompetitive antagonist ameliorates the progression of amytrophic lateral sclerosis-like disease, J. Neurosci. Res., 83, 1134, 10.1002/jnr.20715
Urushitani, 2002, Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis, J. Neurochem., 83, 51030, 10.1046/j.1471-4159.2002.01211.x
Van Damme, 2005, GluR2 deficiency accelerates motor neuron degeneration in a mouse model of amyotrophic lateral sclerosis, J. Neuropathol. Exp. Neurol., 7605
Van Damme, 2003, AMPA receptor antagonist NBQX prolongs survival transgenic mouse model amyotrophic lateral sclerosis, Neurosci. Lett., 343, 281, 10.1016/S0304-3940(03)00314-8
Van Den Bosch, 2006, The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis, Biochim. Biophys. Acta
Vande Velde, 2008, Selective association of misfolded ALS-linked mutant SOD1 with the cytoplasmic face of mitochondria, Proc. Natl Acad. Sci. USA, 104022
Vielhaber, 2000, Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis, Brain, 123, 1339, 10.1093/brain/123.7.1339
Vijayvergiya, 2005, Mutant superoxide dismutase 1 forms aggregates in the brain mitochondrial matrix of amyotrophic lateral sclerosis mice, J. Neurosci., 102463
von Lewinski, 2008, Low Ca2+ buffering in hypoglossal motoneurons of mutant SOD1 (G93A) mice, Neurosci. Lett., 3224
Waza, 2005, 17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration, Nat. Med., 101088
Wiedemann, 1998, Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis, J. Neurol. Sci., 156, 65, 10.1016/S0022-510X(98)00008-2
Williams, 1997, Calcium-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors: a molecular determinant of selective vulnerability in amyotrophic lateral sclerosis, Ann. Neurol., 2200
Wong, 1995, An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria, Neuron, 61105