生物
线粒体
细胞生物学
线粒体分裂
程序性细胞死亡
线粒体融合
细胞凋亡
效应器
凋亡体
半胱氨酸蛋白酶
细胞色素c
DNAJA3公司
秀丽隐杆线虫
线粒体DNA
胞浆
线粒体凋亡诱导通道
遗传学
生物化学
基因
酶
作者
Grazia M. Cereghetti,Luca Scorrano
出处
期刊:Oncogene
[Springer Nature]
日期:2006-08-07
卷期号:25 (34): 4717-4724
被引量:134
标识
DOI:10.1038/sj.onc.1209605
摘要
Mitochondria integrate apoptotic signalling by releasing cytochrome c and other proapoptotic cofactors needed for activation of effector caspases. Previously overlooked morphological changes, mitochondrial fragmentation and cristae remodelling, emerged as subroutines of the mitochondrial programme of apoptosis in mammalian cells, as well as in developmental cell death of Caenorhabditis elegans. Mitochondrial morphology results from fusion and fission processes, controlled by a growing set of 'mitochondria-shaping' proteins. Their levels and function appear to influence mitochondrial pathways of cell death, but mechanisms are largely unknown. An emerging model implicates different signals converging on mitochondria-shaping proteins to activate or deactivate them during apoptosis. In turn, these proteins can orchestrate changes in mitochondrial shape to insure cytochrome c release and progression of the apoptotic cascade. These therefore appear an appealing novel therapeutic target to modulate cell death in cancer.
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