Mitochondrial dynamics and disease, OPA1

被引:174
|
作者
Olichon, Aurelien
Guillou, Emmanuelle
Delettre, Cecile
Landes, Thomas
Arnaune-Pelloquin, Laetitia
Emorine, Laurent J.
Mils, Valerie
Daloyau, Marlene
Hamel, Christian
Amati-Bonneau, Patrizia
Bonneau, Dominique
Reynier, Pascal
Lenaers, Guy
Belenguer, Pascale
机构
[1] Univ Toulouse 3, Lab Biol Cellulaire & Mol Controle Proliferat, F-31062 Toulouse, France
[2] Inst Neurosci Montpellier, INSERM U583, Montpellier, France
[3] INSERM U694, Angers, France
[4] CHU Angers, Lab Biochim & Biol Mol, Angers, France
[5] CHU Angers, Gen Med Serv, Angers, France
来源
关键词
mitochondria; optic atrophy; dynamin; apoptosis; OPA1;
D O I
10.1016/j.bbamcr.2006.04.003
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
The mitochondria are dynamic organelles that constantly fuse and divide. An equilibrium between fusion and fission controls the morphology of the mitochondria, which appear as dots or elongated tubules depending the prevailing force. Characterization of the components of the fission and fusion machineries has progressed considerably, and the emerging question now is what role mitochondrial dynamics play in mitochondrial and cellular functions. Its importance has been highlighted by the discovery that two human diseases are caused by mutations in the two mitochondrial pro-fusion genes, MFN2 and OPA1. This review will focus on data concerning the function of OPA1, mutations in which cause optic atrophy, with respect to the underlying pathophysiological processes. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:500 / 509
页数:10
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