Bcl-2 and Bcl-xL play important roles in the crosstalk between autophagy and apoptosis

被引:401
作者
Zhou, Feifan
Yang, Ying
Xing, Da [1 ]
机构
[1] S China Normal Univ, Coll Biophoton, MOE Key Lab Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; autophagy; Bcl-2; Bcl-xL; Beclin; 1; MALIGNANT GLIOMA-CELLS; CYTOCHROME-C RELEASE; JNK1-MEDIATED PHOSPHORYLATION; PROAPOPTOTIC BAX; FAMILY PROTEINS; ION-CHANNEL; IN-VIVO; DEATH; MITOCHONDRIA; BCL-X(L);
D O I
10.1111/j.1742-4658.2010.07965.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 Ca2+ 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.
引用
收藏
页码:403 / 413
页数:11
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