Controlling the cell death mediators Bax and Bak - Puzzles and conundrums

被引:55
|
作者
Fletcher, Jamie I. [1 ]
Huang, David C. S. [1 ]
机构
[1] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
关键词
Bax; Bak; Bcl-2; pro-survival; apoptosis; BH3;
D O I
10.4161/cc.7.1.5178
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In spite of the available genetic, biochemical and structural data, precisely how the initiators of apoptosis, the BH3-only proteins, trigger Bax and Bak to cause organellar damage remains highly contentious. A widely accepted model suggests that these two critical mediators of apoptosis remain inert until they are directly activated by a subclass of BH3-only proteins including Bim, Bid, and possibly Puma. However, our recent work showed that these death ligands are dispensable for apoptosis to proceed, whereas neutralization of the pro-survival Bcl-2 proteins is essential. These findings challenge current assumptions about how the BH3-only proteins provoke apoptotic cell death and have implications for the development of therapeutics to interfere with the Bcl-2 regulated apoptotic pathway for treating diseases such as cancer.
引用
收藏
页码:39 / 44
页数:6
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