Programming axonal mitochondrial maintenance and bioenergetics in neurodegeneration and regeneration

被引:129
作者
Cheng, Xiu-Tang [1 ]
Huang, Ning [1 ]
Sheng, Zu-Hang [1 ]
机构
[1] NINDS, Porter Neurosci Res Ctr, Synapt Funct Sect, NIH, Room 2B-215,35 Convent Dr, Bethesda, MD 20892 USA
关键词
ORAL CREATINE SUPPLEMENTATION; ACTIVITY-DEPENDENT REGULATION; TRAUMATIC BRAIN-INJURY; DOMINANT OPTIC ATROPHY; PARKIN-DEFICIENT MICE; KINESIN HEAVY-CHAIN; SPINAL-CORD-INJURY; A-CHIP REVEALS; MOUSE MODEL; IN-VIVO;
D O I
10.1016/j.neuron.2022.03.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitochondria generate ATP essential for neuronal growth, function, and regeneration. Due to their polarized structures, neurons face exceptional challenges to deliver mitochondria to and maintain energy homeostasis throughout long axons and terminal branches where energy is in high demand. Chronic mitochondrial dysfunction accompanied by bioenergetic failure is a pathological hallmark of major neurodegenerative diseases. Brain injury triggers acute mitochondrial damage and a local energy crisis that accelerates neuron death. Thus, mitochondrial maintenance defects and axonal energy deficits emerge as central problems in neurodegenerative disorders and brain injury. Recent studies have started to uncover the intrinsic mechanisms that neurons adopt to maintain (or reprogram) axonal mitochondrial density and integrity, and their bioenergetic capacity, upon sensing energy stress. In this review, we discuss recent advances in how neurons maintain a healthy pool of axonal mitochondria, as well as potential therapeutic strategies that target bioenergetic restoration to power neuronal survival, function, and regeneration.
引用
收藏
页码:1899 / 1923
页数:25
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