Mitochondrial control of caspase-dependent and -independent cell death

被引:281
|
作者
Pradelli, Ludivine A. [1 ,3 ]
Beneteau, Marie [1 ,3 ]
Ricci, Jean-Ehrland [1 ,2 ,3 ]
机构
[1] Univ Nice Sophia Antipolis, Fac Med, F-06107 Nice 2, France
[2] Ctr Hosp Univ Nice, Dept Anesthesie Reanimat, F-06202 Nice 3, France
[3] Equipe 3 AVENIR, Ctr Mediterraneen Med Mol C3M, INSERM, U895, F-06204 Nice 3, France
关键词
Mitochondria; Bcl-2; family; Cell death; Apoptosis; Caspase-independent cell death; Mitochondrial outer membrane permeabilization; Cancer; BH3; mimetics; OUTER-MEMBRANE PERMEABILIZATION; SERINE-PROTEASE HTRA2/OMI; CYTOCHROME-C RELEASE; HUMAN LEUKEMIC-CELLS; ENDONUCLEASE-G; BCL-2; FAMILY; INDUCED APOPTOSIS; MYELOID-LEUKEMIA; BREAST-CANCER; TNF-ALPHA;
D O I
10.1007/s00018-010-0285-y
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
Mitochondria control whether a cell lives or dies. The role mitochondria play in deciding the fate of a cell was first identified in the mid-1990s, because mitochondria-enriched fractions were found to be necessary for activation of death proteases, the caspases, in a cell-free model of apoptotic cell death. Mitochondrial involvement in apoptosis was subsequently shown to be regulated by Bcl-2, a protein that was known to contribute to cancer in specific circumstances. The important role of mitochondria in promoting caspase activation has therefore been a major focus of apoptosis research; however, it is also clear that mitochondria contribute to cell death by caspase-independent mechanisms. In this review, we will highlight recent findings and discuss the mechanism underlying the mitochondrial control of apoptosis and caspase-independent cell death.
引用
收藏
页码:1589 / 1597
页数:9
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