Mitochondrial outer-membrane permeabilization and remodelling in apoptosis

被引:103
作者
Jourdain, Alexis [1 ]
Martinou, Jean-Claude [1 ]
机构
[1] Univ Geneva, Dept Cell Biol, CH-1211 Geneva 4, Switzerland
关键词
Apoptosis; Mitochondria; Bax; Bcl-2; Drp-1; Mitochondrial fusion; Mitochondrial fission; CYTOCHROME-C RELEASE; BCL-2 PROTEIN FAMILY; DYNAMIN-RELATED GTPASE; PROGRAMMED CELL-DEATH; MARIE-TOOTH-DISEASE; MAMMALIAN-CELLS; CONFORMATIONAL-CHANGE; PROTEOLYTIC CLEAVAGE; FISSION MACHINERY; TRIGGER APOPTOSIS;
D O I
10.1016/j.biocel.2009.05.001
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
Many human pathologies are associated with defects in mitochondria such as diabetes, neurodegenerative diseases or cancer. This tiny organelle is involved in a plethora of processes in mammalian cells, including energy production, lipid metabolism and cell death. In the so-called intrinsic apoptotic pathway, the outer mitochondrial membrane (MOM) is premeabilized by the pro-apoptotic Bcl-2 members Bax and Bak, allowing the release of apoptogenic factors such as cytochrome c from the inter-membrane space into the cytosol. At the same time, mitochondria fragment in response to Drp-1 activation suggesting that mitochondrial fission could play a role in mitochondrial outer-membrane permeabilization (MOMP). In this review, we will discuss the link that could exist between mitochondrial fission and fusion machinery, Bcl-2 family members and MOMP. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1884 / 1889
页数:6
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