内质网
自噬
细胞生物学
生物
碎片(计算)
高尔基体
膜曲率
溶酶体
未折叠蛋白反应
膜
生物化学
酶
生态学
小泡
细胞凋亡
作者
Andrea Gubaš,Ivan Đikić
出处
期刊:Molecular Cell
[Elsevier]
日期:2022-04-01
卷期号:82 (8): 1492-1500
被引量:64
标识
DOI:10.1016/j.molcel.2022.02.018
摘要
Summary
The endoplasmic reticulum (ER) is a hotspot for many essential cellular functions. The ER membrane is highly dynamic, which affects many cellular processes that take place within the ER. One such process is ER-phagy, a selective degradation of ER fragments (including membranes and luminal content), which serves to preserve the size of ER while adapting its morphology under basal and stress conditions. In order to be degraded, the ER undergoes selective fragmentation facilitated by specialized ER-shaping proteins that also act as ER-phagy receptors. Their ability to sense and induce membrane curvature, as well as to bridge the ER with autophagy machinery, allows for a successful ER fragmentation and delivery of these fragments to the lysosome for degradation and recycling. In this review, we provide insights into ER-phagy from the perspective of membrane remodeling. We highlight the importance of ER membrane dynamics during ER-phagy and emphasize how its dysregulation reflects on human physiology and pathology.
科研通智能强力驱动
Strongly Powered by AbleSci AI