Mitochondria at the neuronal presynapse in health and disease

被引:411
作者
Devine, Michael J. [1 ]
Kittler, Josef T. [1 ]
机构
[1] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
基金
欧洲研究理事会; 英国惠康基金;
关键词
DYNAMIN-RELATED PROTEIN-1; AMYLOID BETA-PEPTIDE; ACTIVITY-DEPENDENT REGULATION; SYNAPTIC VESICLE ENDOCYTOSIS; TARGETED ANTIOXIDANT MITOQ; MOTOR-NERVE TERMINALS; AXONAL-TRANSPORT; ALPHA-SYNUCLEIN; ALZHEIMERS-DISEASE; IN-VIVO;
D O I
10.1038/nrn.2017.170
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synapses enable neurons to communicate with each other and are therefore a prerequisite for normal brain function. Presynaptically, this communication requires energy and generates large fluctuations in calcium concentrations. Mitochondria are optimized for supplying energy and buffering calcium, and they are actively recruited to presynapses. However, not all presynapses contain mitochondria; thus, how might synapses with and without mitochondria differ? Mitochondria are also increasingly recognized to serve additional functions at the presynapse. Here, we discuss the importance of presynaptic mitochondria in maintaining neuronal homeostasis and how dysfunctional presynaptic mitochondria might contribute to the development of disease.
引用
收藏
页码:63 / 80
页数:18
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