Neuronal autophagy and axon degeneration

Neuronal autophagy and axon degeneration
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神经元自噬和轴突变性

DOI:
10.1007/s00018-018-2812-1
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发表时间:
2018-04
影响因子:
8
通讯作者:
Song Fuyong
Song Fuyong
中科院分区:
生物学1区
文献类型:
--
作者:
Wang Yu;Song Mingxue;Song Fuyong

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轴突退变是轴突死亡和分解的病理生理过程,其特征在于若干形态学特征,包括轴质细胞器的积聚、微管的解体以及轴突细胞的破碎。
Axon degeneration is a pathophysiological process of axonal dying and breakdown, which is characterized by several morphological features including the accumulation of axoplasmic organelles, disassembly of microtubules, and fragmentation of the axonal cytoskeleton. Autophagy, a highly conserved lysosomal-degradation machinery responsible for the control of cellular protein quality, is widely believed to be essential for the maintenance of axonal homeostasis in neurons. In recent years, more and more evidence suggests that dysfunctional autophagy is associated with axonal degeneration in many neurodegenerative diseases. Here, we review the core machinery of autophagy in neuronal cells, and provide several major steps that interfere with autophagy flux in neurodegenerative conditions. Furthermore, this review highlights the potential role of neuronal autophagy in axon degeneration, and presents some possible molecular mechanisms by which dysfunctional autophagy leads to axon degeneration in pathological conditions.
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