Mitochondria, calcium-dependent neuronal death and neurodegenerative disease

被引:144
作者
Duchen, Michael R. [1 ]
机构
[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2012年 / 464卷 / 01期
基金
英国惠康基金; 英国医学研究理事会;
关键词
Mitochondria; Intracellular calcium; Neurodegenerative disease; Glutamate excitotoxicity; PERMEABILITY TRANSITION PORE; CA-2&-INDUCED MEMBRANE TRANSITION; MOTOR-NERVE TERMINALS; NMDA RECEPTOR ACTIVATION; RAT HIPPOCAMPAL-NEURONS; CELL-DEATH; POLY(ADP-RIBOSE) POLYMERASE; PARKINSONS-DISEASE; GLUTAMATE EXCITOTOXICITY; NITRIC-OXIDE;
D O I
10.1007/s00424-012-1112-0
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Understanding the mechanisms of neuronal dysfunction and death represents a major frontier in contemporary medicine, involving the acute cell death in stroke, and the attrition of the major neurodegenerative diseases, including Parkinson's, Alzheimer's, Huntington's and Motoneuron diseases. A growing body of evidence implicates mitochondrial dysfunction as a key step in the pathogenesis of all these diseases, with the promise that mitochondrial processes represent valuable potential therapeutic targets. Each disease is characterised by the loss of a specific vulnerable population of cells-dopaminergic neurons in Parkinson's disease, spinal motoneurons in Motoneuron disease, for example. We discuss the possible roles of cell type-specific calcium signalling mechanisms in defining the pathological phenotype of each of these major diseases and review central mechanisms of calcium-dependent mitochondrial-mediated cell death.
引用
收藏
页码:111 / 121
页数:11
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