细胞凋亡
细胞生物学
胞浆
Bcl-2相关X蛋白
线粒体
生物
Bcl-2家族
凋亡体
内源性凋亡
凋亡结构域抑制剂
程序性细胞死亡
半胱氨酸蛋白酶
遗传学
半胱氨酸蛋白酶3
生物化学
酶
标识
DOI:10.1016/j.bbrc.2017.06.190
摘要
Proteins of the B-cell lymphoma-2 (BCL-2) family control the intrinsic apoptosis pathway. The pro-apoptotic BCL-2 proteins BAX and BAK can commit a cell to its programmed death by permeabilizing the outer mitochondrial membrane (OMM) and subsequent initiation of the caspase cascade. Therefore, the activities of BAX and BAK are precisely controlled by a complex network of proteins inside and outside the BCL-2 family. Cells survive by constant control of dynamic translocation and retrotranslocation of BAX and BAK to the mitochondria and back into the cytosol. Recent insights into BAX/BAK shuttling, BCL-2 protein interactions, the role of BH3-only proteins in apoptosis signaling and the active BAX complex set the stage for the development of novel strategies in cancer therapy and the analysis of cellular predisposition to apoptosis.
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