自噬
ATG5型
细胞凋亡
细胞生物学
生物
Bcl xL型
Bcl-2家族
癌变
程序性细胞死亡
串扰
坏死性下垂
化学
线粒体
细胞
遗传学
基因
物理
光学
作者
Feifan Zhou,Ying Yang,Da Xing
出处
期刊:FEBS Journal
[Wiley]
日期:2010-12-23
卷期号:278 (3): 403-413
被引量:352
标识
DOI:10.1111/j.1742-4658.2010.07965.x
摘要
Autophagy and apoptosis play important roles in the development, cellular homeostasis and, especially, oncogenesis of mammals. They may be triggered by common upstream signals, resulting in combined autophagy and apoptosis. In other instances, they may be mutually exclusive. Recent studies have suggested possible molecular mechanisms for crosstalk between autophagy and apoptosis. Bcl‐2 and Bcl‐xL, the well‐characterized apoptosis guards, appear to be important factors in autophagy, inhibiting Beclin 1‐mediated autophagy by binding to Beclin 1. In addition, Beclin 1, Bcl‐2 and Bcl‐xL can cooperate with Atg5 or Ca 2+ to regulate both autophagy and apoptosis. Thus, Bcl‐2 and Bcl‐xL represent a molecular link between autophagy and apoptosis. Here, we discuss the possible roles of Bcl‐2 and Bcl‐xL in apoptosis and autophagy, and the crosstalk between them.
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