自噬
伴侣(临床)
神经保护
细胞生物学
生物
神经毒性
程序性细胞死亡
平衡
神经退行性变
ULK1
神经科学
化学
医学
生物化学
细胞凋亡
疾病
磷酸化
安普克
有机化学
病理
蛋白激酶A
毒性
作者
Qi Jia,Li Jin,Xiaofeng Guo,Yang Li,You Wu,Yuliang Peng,Zongping Fang,Xijing Zhang
标识
DOI:10.4103/1673-5374.385848
摘要
Abstract Chaperone-mediated autophagy is one of three types of autophagy and is characterized by the selective degradation of proteins. Chaperone-mediated autophagy contributes to energy balance and helps maintain cellular homeostasis, while providing nutrients and support for cell survival. Chaperone-mediated autophagy activity can be detected in almost all cells, including neurons. Owing to the extreme sensitivity of neurons to their environmental changes, maintaining neuronal homeostasis is critical for neuronal growth and survival. Chaperone-mediated autophagy dysfunction is closely related to central nervous system diseases. It has been shown that neuronal damage and cell death are accompanied by chaperone-mediated autophagy dysfunction. Under certain conditions, regulation of chaperone-mediated autophagy activity attenuates neurotoxicity. In this paper, we review the changes in chaperone-mediated autophagy in neurodegenerative diseases, brain injury, glioma, and autoimmune diseases. We also summarize the most recent research progress on chaperone-mediated autophagy regulation and discuss the potential of chaperone-mediated autophagy as a therapeutic target for central nervous system diseases.
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