自噬
泛素
蛋白酶体
细胞生物学
蛋白质聚集
蛋白质降解
未折叠蛋白反应
细胞内
程序性细胞死亡
细胞凋亡
生物
化学
生物化学
内质网
基因
作者
Yanan Li,Shujing Li,Harry X. Wu
出处
期刊:Cells
[MDPI AG]
日期:2022-03-01
卷期号:11 (5): 851-851
被引量:53
标识
DOI:10.3390/cells11050851
摘要
In response to environmental stimuli, cells make a series of adaptive changes to combat the injury, repair the damage, and increase the tolerance to the stress. However, once the damage is too serious to repair, the cells will undergo apoptosis to protect the overall cells through suicidal behavior. Upon external stimulation, some intracellular proteins turn into unfolded or misfolded protein, exposing their hydrophobic regions to form protein aggregation, which may ultimately produce serious damage to the cells. Ubiquitin plays an important role in the degradation of these unnatural proteins by tagging with ubiquitin chains in the ubiquitin-proteasome or autophagy system. If the two processes fail to eliminate the abnormal protein aggregates, the cells will move to apoptosis and death. Dysregulation of ubiquitin-proteasome system (UPS) and autophagy may result in the development of numerous diseases. This review focuses on the molecular mechanisms of UPS and autophagy in clearance of intracellular protein aggregates, and the relationship between dysregulation of ubiquitin network and diseases.
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