Molecular mechanisms and physiologic functions of mitochondrial dynamics

被引:201
|
作者
Otera, Hidenori [1 ]
Mihara, Katsuyoshi [1 ]
机构
[1] Kyushu Univ, Dept Mol Biol, Grad Sch Med Sci, Fukuoka 8128582, Japan
来源
JOURNAL OF BIOCHEMISTRY | 2011年 / 149卷 / 03期
基金
日本学术振兴会;
关键词
Mfn1; 2; Opa1; Drp1; GTPase; mitochondrial dynamics; DIFFERENTIATION-ASSOCIATED PROTEIN-1; DOMINANT OPTIC ATROPHY; CYTOCHROME-C RELEASE; M-AAA PROTEASE; AXONAL-TRANSPORT; PARKINSONS-DISEASE; CELL-PROLIFERATION; OPA1; FISSION; DRP1;
D O I
10.1093/jb/mvr002
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 are highly dynamic organelles that continuously change their shape through frequent fusion, fission and movement throughout the cell, and these dynamics are crucial for the life and death of the cells as they have been linked to apoptosis, maintenance of cellular homeostasis, and ultimately to neurologic disorders and metabolic diseases. Over the past decade, a growing number of novel proteins that regulate mitochondrial dynamics have been discovered. Large GTPase family proteins and their regulators control these aspects of mitochondrial dynamics. In this review, we briefly summarize the current knowledge about molecular machineries regulating mitochondrial fusion/fission and the role of mitochondrial dynamics in cell pathophysiology.
引用
收藏
页码:241 / 251
页数:11
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