瓦勒氏变性
变性(医学)
细胞生物学
神经退行性变
线粒体
再生(生物学)
轴突切开术
程序性细胞死亡
神经保护
品脱1
作者
Matthew D. Figley,Aaron DiAntonio
标识
DOI:10.1016/j.conb.2020.02.012
摘要
Axons are essential for nervous system function and axonal pathology is a common hallmark of many neurodegenerative diseases. Over a century and a half after the original description of Wallerian axon degeneration, advances over the past five years have heralded the emergence of a comprehensive, mechanistic model of an endogenous axon degenerative process that can be activated by both injury and disease. Axonal integrity is maintained by the opposing actions of the survival factors NMNAT2 and STMN2 and pro-degenerative molecules DLK and SARM1. The balance between axon survival and self-destruction is intimately tied to axonal NAD+ metabolism. These mechanistic insights may enable axon-protective therapies for a variety of human neurodegenerative diseases including peripheral neuropathy, traumatic brain injury and potentially ALS and Parkinson's.
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