Mitochondrial intermembrane proteins in cell death

被引:326
作者
van Gurp, M
Festjens, N
van Loo, G
Saelens, X
Vandenabeele, P
机构
[1] VIB, Mol Signaling & Cell Death Unit, Dept Mol Biomed Res, B-9000 Ghent, Belgium
[2] Univ Ghent, B-9000 Ghent, Belgium
关键词
mitochondria; cytochrome c; Smac/DIABLO; Omi/HtrA2; endonuclease G; Acyl-CoA-binding protein; AIF; apoptosis; caspase;
D O I
10.1016/S0006-291X(03)00621-1
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
Apoptosis is a form of programmed cell death important in the development and tissue homeostasis of multicellular organisms. Mitochondria have, next to their function in respiration, an important role in the apoptotic-signaling pathway. Malfunctioning at any level of the cell is eventually translated in the release of apoptogenic factors from the mitochondrial intermembrane space resulting in the organized demise of the cell. Some of these factors, such as AIF and endonuclease G, appear to be highly conserved during evolution. Other factors, like cytochrome e, have gained their apoptogenic function later during evolution. In this review, we focus on the role of cytochrorne c, AIF, endonuclease G, Smac/DIABLO, Omi/HtrA2, Acyl-CoA-binding protein, and polypyrimidine tract-binding protein in the initiation and modulation of cell death in different model organisms. These mitochondrial factors may contribute to both caspase-dependent and caspase-independent processes in apoptotic cell death. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:487 / 497
页数:11
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