自噬
神经退行性变
细胞生物学
生物
程序性细胞死亡
细胞器
线粒体
神经科学
遗传学
细胞凋亡
医学
病理
疾病
作者
Angeleen Fleming,Mathieu Bourdenx,Motoki Fujimaki,Cansu Karabiyik,Gregory J. Krause,Ana López,Adrián Martín‐Segura,Claudia Puri,Aurora Scrivo,John Skidmore,Sung Min Son,Eleanna Stamatakou,Lidia Wróbel,Ye Zhu,Ana María Cuervo,David C. Rubinsztein
出处
期刊:Neuron
[Cell Press]
日期:2022-02-07
卷期号:110 (6): 935-966
被引量:261
标识
DOI:10.1016/j.neuron.2022.01.017
摘要
The term autophagy encompasses different pathways that route cytoplasmic material to lysosomes for degradation and includes macroautophagy, chaperone-mediated autophagy, and microautophagy. Since these pathways are crucial for degradation of aggregate-prone proteins and dysfunctional organelles such as mitochondria, they help to maintain cellular homeostasis. As post-mitotic neurons cannot dilute unwanted protein and organelle accumulation by cell division, the nervous system is particularly dependent on autophagic pathways. This dependence may be a vulnerability as people age and these processes become less effective in the brain. Here, we will review how the different autophagic pathways may protect against neurodegeneration, giving examples of both polygenic and monogenic diseases. We have considered how autophagy may have roles in normal CNS functions and the relationships between these degradative pathways and different types of programmed cell death. Finally, we will provide an overview of recently described strategies for upregulating autophagic pathways for therapeutic purposes.
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