Opening the doors to cytochrome c: Changes in mitochondrial shape and apoptosis

被引:117
作者
Scorrano, Luca [1 ,2 ]
机构
[1] Univ Geneva, Dept Cell Physiol & Metab, Sch Med, CH-1211 Geneva, Switzerland
[2] Venetian Inst Mol Med, Dulbecco Telethon Inst, I-35129 Padua, Italy
关键词
Mitochondria; Apoptosis; Fusion; Fission; Cristae remodeling; PROGRAMMED CELL-DEATH; WOLF-HIRSCHHORN-SYNDROME; DYNAMIN-RELATED GTPASE; INTRAMEMBRANE SERINE PROTEASES; DEPENDENT PROTEIN-KINASE; DOMINANT OPTIC ATROPHY; ENDOPLASMIC-RETICULUM; MAMMALIAN-CELLS; INNER-MEMBRANE; PROTEOLYTIC CLEAVAGE;
D O I
10.1016/j.biocel.2009.04.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Mitochondria are key organelles in the regulation of apoptosis induced by intrinsic stimuli. This is accomplished by the release in the cytoplasm of cytochrome c and of other cofactors that ensure the activation of effector caspases. Multiple changes in the shape of the organelle occur around the time of the release of these factors, including fragmentation of the mitochondrial network and the activation of the so-called "cristae remodeling" pathway. However, contrasting evidence exist on the functional role of these changes. Here we review the molecular mechanisms that control mitochondrial shape, their changes during apoptosis and the role that these changes might play in the amplification of the apoptotic cascade. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1875 / 1883
页数:9
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