Brain mitochondrial calcium transport: Origins of the set-point concept and its application to physiology and pathology

被引:22
作者
Nicholls, David G. [1 ]
机构
[1] Buck Inst Res Aging, 8001 Redwood Bld, Novato, CA 94945 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
Mitochondria; Calcium; Brain; Set-point; Excitotoxicity; RAT-LIVER MITOCHONDRIA; CEREBELLAR GRANULE CELLS; ACUTE GLUTAMATE EXCITOTOXICITY; INTACT SYNAPTOSOMES; PLASMA-MEMBRANE; NERVE-TERMINALS; ION TRANSPORT; DEPOLARIZATION; ACCUMULATION; REEVALUATION;
D O I
10.1016/j.neuint.2016.12.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transport of calcium across the inner mitochondrial membrane plays a key role in neuronal physiology and pathology. The kinetic responses of the uniporter and efflux pathways are such that a cytosolic free calcium 'set-point' can be established - above which there is net calcium accumulation into the matrix that is reversed when plasma membrane transport lowers cytosolic calcium. Pathological activation of N-methyl-D-aspartate receptor mediated sodium and calcium entry into the neuron, as occurs in stroke and spreading depression, places severe demands on both the ATP-generating and calcium loading capacities of the neuronal mitochondria as the set-point is exceeded. Experiments that led to the concept of the set-point are reviewed. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5 / 12
页数:8
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