蛋白质稳态
自噬
老化
蛋白酶体
泛素
蛋白质降解
内质网相关蛋白降解
串扰
细胞生物学
蛋白质组
生物
溶酶体
未折叠蛋白反应
生物化学
内质网
细胞凋亡
遗传学
酶
基因
光学
物理
作者
Jia Liang Sun‐Wang,Saška Ivanova,António Zorzano
标识
DOI:10.1016/j.arr.2020.101203
摘要
Dysregulated proteostasis is one of the hallmarks of ageing. Damaged proteins may impair cellular function and their accumulation may lead to tissue dysfunction and disease. This is why protective mechanisms to safeguard the cell proteome have evolved. These mechanisms consist of cellular machineries involved in protein quality control, including regulators of protein translation, folding, trafficking and degradation. In eukaryotic cells, protein degradation occurs via two main pathways: the ubiquitin-proteasome system (UPS) and the autophagy-lysosome pathway. Although distinct pathways, they are not isolated systems and have a complementary nature, as evidenced by recent studies. These findings raise the question of how autophagy and the proteasome crosstalk. In this review we address how the two degradation pathways impact each other, thereby adding a new layer of regulation to protein degradation. We also analyze the implications of the UPS and autophagy in ageing.
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