Mitochondria, calcium and cell death: a deadly triad in neurodegeneration

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Mitochondria, calcium and cell death: a deadly triad in neurodegeneration is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1016/J.BBABIO.2009.02.021
P3181OpenCitations bibliographic resource ID4906580
P932PMC publication ID2696196
P698PubMed publication ID19268425
P5875ResearchGate publication ID24183987

P50authorPaola PizzoQ58873319
Fulvio CelsiQ54449613
Carmen FotinoQ57528501
Paolo PintonQ37374908
Marisa BriniQ39956417
Rosario RizzutoQ41312267
P2093author name stringSara Leo
P2860cites workParkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activityQ22254785
Presenilins form ER Ca2+ leak channels, a function disrupted by familial Alzheimer's disease-linked mutationsQ24301868
Familial Alzheimer disease-linked mutations specifically disrupt Ca2+ leak function of presenilin 1Q24302464
Recombinant expression of the Ca(2+)-sensitive aspartate/glutamate carrier increases mitochondrial ATP production in agonist-stimulated Chinese hamster ovary cellsQ24307541
Huntingtin and huntingtin-associated protein 1 influence neuronal calcium signaling mediated by inositol-(1,4,5) triphosphate receptor type 1Q24310249
Parkin is recruited selectively to impaired mitochondria and promotes their autophagyQ24317471
Localization of LRRK2 to membranous and vesicular structures in mammalian brainQ24318643
PINK1 is necessary for long term survival and mitochondrial function in human dopaminergic neuronsQ24322788
Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell deathQ28242641
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseasesQ28269333
Normal huntingtin function: an alternative approach to Huntington's diseaseQ28281904
Nicastrin, presenilin, APH-1, and PEN-2 form active gamma-secretase complexes in mitochondriaQ28285347
The Ca2+ concentration of the endoplasmic reticulum is a key determinant of ceramide-induced apoptosis: significance for the molecular mechanism of Bcl-2 actionQ28366131
DJ-1 gene deletion reveals that DJ-1 is an atypical peroxiredoxin-like peroxidaseQ28513159
Cyclophilin D is a component of mitochondrial permeability transition and mediates neuronal cell death after focal cerebral ischemiaQ28585666
Mitochondrial dysfunction and oxidative damage in parkin-deficient miceQ28593859
Innovation: Looking forward to seeing calciumQ29040650
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkinQ29615684
Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of Drosophila Pink1 is rescued by ParkinQ29617063
The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in DrosophilaQ29617091
Kinetics of mitochondrial calcium transport. II. A kinetic description of the sodium-dependent calcium efflux mechanism of liver mitochondria and inhibition by ruthenium red and by tetraphenylphosphoniumQ68976622
Presenilin-1 mutations increase levels of ryanodine receptors and calcium release in PC12 cells and cortical neuronsQ73675821
Control of InsP3-induced Ca2+ oscillations in permeabilized blowfly salivary gland cells: contribution of mitochondriaQ73900892
VOLUME CHANGES INDUCED BY INORGANIC PHOSPHATE IN LIVER MITOCHONDRIAQ78542414
Are mitochondria critical in the pathogenesis of Alzheimer's disease?Q81440649
Up-regulation of inositol 1,4,5-trisphosphate receptor type 1 is responsible for a decreased endoplasmic-reticulum Ca2+ content in presenilin double knock-out cellsQ83288026
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegenerationQ45302924
Increased caspase-2, calpain activations and decreased mitochondrial complex II activity in cells expressing exogenous huntingtin exon 1 containing CAG repeat in the pathogenic rangeQ45306567
PS2 mutation increases neuronal cell vulnerability to neurotoxicants through activation of caspase-3 by enhancing of ryanodine receptor-mediated calcium releaseQ46880293
Clusters of hyperactive neurons near amyloid plaques in a mouse model of Alzheimer's diseaseQ48920532
Copper-dependent inhibition of human cytochrome c oxidase by a dimeric conformer of amyloid-beta1-42.Q49134222
Chronic exposure to sub-lethal beta-amyloid (Abeta) inhibits the import of nuclear-encoded proteins to mitochondria in differentiated PC12 cells.Q50665343
Different species of alpha-synuclein oligomers induce calcium influx and seeding.Q52581429
Cytochrome oxidase deficiency in Alzheimer's disease.Q53181028
Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide.Q53216314
Presenilin mutations linked to familial Alzheimer's disease reduce endoplasmic reticulum and Golgi apparatus calcium levels.Q53277217
A selective defect of cytochrome c oxidase is present in brain of Alzheimer disease patients.Q53341470
Presenilins and Alzheimer disease: the calcium conspiracy.Q53382538
Beta-amyloid precursor protein is a direct cleavage target of HtrA2 serine protease. Implications for the physiological function of HtrA2 in the mitochondria.Q53588924
Regulation of Ca2+ Efflux in Rat Liver Mitochondria. Role of Membrane PotentialQ58454407
Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivatorsQ29617353
Amyloid precursor protein trafficking, processing, and functionQ29617429
BAX and BAK regulation of endoplasmic reticulum Ca2+: a control point for apoptosisQ29620466
Impact of mitochondrial Ca2+ cycling on pattern formation and stabilityQ30447507
Nitric oxide-induced mitochondrial fission is regulated by dynamin-related GTPases in neurons.Q30477849
SERCA pump activity is physiologically regulated by presenilin and regulates amyloid beta productionQ30482542
N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial traffickingQ30486372
Evidence that mitochondria buffer physiological Ca2+ loads in lizard motor nerve terminalsQ32067534
Brain lesions, obesity, and other disturbances in mice treated with monosodium glutamateQ34054189
Imaging the permeability pore transition in single mitochondriaQ34167671
Complex I and Parkinson's diseaseQ34499041
Thirty years of Alzheimer's disease genetics: the implications of systematic meta-analysesQ34831241
Calcium dyshomeostasis and intracellular signalling in Alzheimer's diseaseQ34988301
Historical review: mitochondria and calcium: ups and downs of an unusual relationshipQ35114277
Calpain-cleavage of alpha-synuclein: connecting proteolytic processing to disease-linked aggregationQ35757239
Deranged neuronal calcium signaling and Huntington disease.Q35874324
Chaperone-mediated coupling of endoplasmic reticulum and mitochondrial Ca2+ channels.Q36119444
Calcium dysregulation in Alzheimer's disease: recent advances gained from genetically modified animalsQ36241923
Mitochondrial participation in the intracellular Ca2+ networkQ36254615
3-Nitropropionic acid: a mitochondrial toxin to uncover physiopathological mechanisms underlying striatal degeneration in Huntington's disease.Q36318579
Mitochondrial targeting and a novel transmembrane arrest of Alzheimer's amyloid precursor protein impairs mitochondrial function in neuronal cellsQ36323368
Microdomains of intracellular Ca2+: molecular determinants and functional consequences.Q36350079
Optical probing of neuronal circuit dynamics: genetically encoded versus classical fluorescent sensors.Q36380371
Gene expression-based screening identifies microtubule inhibitors as inducers of PGC-1alpha and oxidative phosphorylationQ36534424
Mitochondrial alterations in Alzheimer's diseaseQ36549402
Parkin and defective ubiquitination in Parkinson's diseaseQ36611521
Regulation of mitochondrial ATP synthesis by calcium: evidence for a long-term metabolic primingQ36702104
Calcium and neurodegenerationQ36747495
Biosensors for the detection of calcium and pH.Q36796229
Targeting aequorin and green fluorescent protein to intracellular organellesQ36807899
Pink1, Parkin, DJ-1 and mitochondrial dysfunction in Parkinson's diseaseQ36820873
The daily job of night killers: alternative roles of the BCL-2 family in organelle physiologyQ37031106
Mitochondria in the aetiology and pathogenesis of Parkinson's diseaseQ37037953
Mitochondrial Ca2+ and the heartQ37051821
Mitochondrial dynamics: to be in good shape to surviveQ37108458
VDAC regulation: role of cytosolic proteins and mitochondrial lipidsQ37163358
Cyclophilin D deficiency attenuates mitochondrial and neuronal perturbation and ameliorates learning and memory in Alzheimer's diseaseQ37463481
Ca2+ as a second messenger within mitochondria of the heart and other tissuesQ37918891
Kinetics of calcium(2+) ion carrier in rat liver mitochondriaQ39291877
Mitochondria exert a negative feedback on the propagation of intracellular Ca2+ waves in rat cortical astrocytesQ39508107
Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium fluxQ39891449
Interplay of the Ca2+-binding protein DREAM with presenilin in neuronal Ca2+ signalingQ39956189
Calcium homeostasis and mitochondrial dysfunction in striatal neurons of Huntington diseaseQ40031554
Transient and long-lasting openings of the mitochondrial permeability transition pore can be monitored directly in intact cells by changes in mitochondrial calcein fluorescenceQ40137371
Apoptotic mechanisms in mutant LRRK2-mediated cell deathQ40149547
Mitochondria are a direct site of A beta accumulation in Alzheimer's disease neurons: implications for free radical generation and oxidative damage in disease progressionQ40301497
Reduction of Ca2+ stores and capacitative Ca2+ entry is associated with the familial Alzheimer's disease presenilin-2 T122R mutation and anticipates the onset of dementia.Q40449011
Parkin protects human dopaminergic neuroblastoma cells against dopamine-induced apoptosisQ40545020
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c releaseQ40551652
The presenilin 2 M239I mutation associated with familial Alzheimer's disease reduces Ca2+ release from intracellular storesQ40581064
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.Q40721588
Modulation of intramitochondrial free Ca2+ concentration by antagonists of Na(+)-Ca2+ exchangeQ40808697
A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiencyQ40938846
New light on mitochondrial calciumQ40978945
Ca2+ homeostasis in the agonist-sensitive internal store: functional interactions between mitochondria and the ER measured In situ in intact cells.Q41010150
Mechanism of Ca2+ disruption in Alzheimer's disease by presenilin regulation of InsP3 receptor channel gating.Q41256595
The permeability transition pore as a mitochondrial calcium release channel: a critical appraisalQ41456661
Presenilin-2 mutations modulate amplitude and kinetics of inositol 1, 4,5-trisphosphate-mediated calcium signalsQ41700856
Apoptosis driven by IP(3)-linked mitochondrial calcium signalsQ42265765
Amyloid beta-induced changes in nitric oxide production and mitochondrial activity lead to apoptosisQ42467635
Active mitochondria surrounding the pancreatic acinar granule region prevent spreading of inositol trisphosphate-evoked local cytosolic Ca(2+) signals.Q42477596
Calcium ion-dependent signalling and mitochondrial dysfunction: mitochondrial calcium uptake during hormonal stimulation in intact liver cells and its implication for the mitochondrial permeability transitionQ42479987
Integrating cytosolic calcium signals into mitochondrial metabolic responsesQ42652819
Oxidative damage is the earliest event in Alzheimer diseaseQ43696731
Beta-amyloid fragment 25-35 causes mitochondrial dysfunction in primary cortical neuronsQ44149266
The mitochondrial calcium uniporter is a highly selective ion channel.Q44737530
Inhibition of mitochondrial Na+-Ca2+ exchange restores agonist-induced ATP production and Ca2+ handling in human complex I deficiency.Q44989706
Bcl-2 and Bax exert opposing effects on Ca2+ signaling, which do not depend on their putative pore-forming regionQ45107840
Cleavage of the plasma membrane Na+/Ca2+ exchanger in excitotoxicityQ45244063
Huntingtin localization in brains of normal and Huntington's disease patientsQ45295341
Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtinQ45297269
Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.Q45302702
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectcell biologyQ7141
biophysicsQ7100
neurodegenerationQ1755122
cell deathQ2383867
mitochondrionQ39572
P304page(s)335-44
P577publication date2009-05-01
P1433published inBiochimica et Biophysica ActaQ864239
P1476titleMitochondria, calcium and cell death: a deadly triad in neurodegeneration
P478volume1787

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