Mitochondrial turnover in the heart

被引:97
作者
Gottlieb, Roberta A. [1 ]
Gustafsson, Asa B. [2 ]
机构
[1] San Diego State Univ, BioSci Ctr, San Diego, CA 92182 USA
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2011年 / 1813卷 / 07期
关键词
Mitochondria; Mitophagy; Autophagy; Mitochondrial turnover; Cardioprotection; DYNAMIN-RELATED PROTEIN; CELL-DEATH; ISCHEMIA/REPERFUSION INJURY; REGULATE PGC-1-ALPHA; OXIDATIVE STRESS; BH3; DOMAIN; AUTOPHAGY; FISSION; BNIP3; PARKIN;
D O I
10.1016/j.bbamcr.2010.11.017
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
Mitochondrial quality control is increasingly recognized as an essential element in maintaining optimally functioning tissues. Mitochondrial quality control depends upon a balance between biogenesis and autophagic destruction. Mitochondrial dynamics (fusion and fission) allows for the redistribution of mitochondrial components. We speculate that this permits sorting of highly functional components into one end of a mitochondrion, while damaged components are segregated at the other end, to be jettisoned by asymmetric fission followed by selective mitophagy. Ischemic preconditioning requires autophagy/mitophagy, resulting in selective elimination of damaged mitochondria, leaving behind a population of robust mitochondria with a higher threshold for opening of the mitochondrial permeability transition pore. In this review we will consider the factors that regulate mitochondrial biogenesis and destruction, the machinery involved in both processes, and the biomedical consequences associated with altered mitochondrial turnover. This article is part of a Special Issue entitled: Mitochondria and Cardioprotection. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1295 / 1301
页数:7
相关论文
共 99 条
[1]   Respiratory Active Mitochondrial Supercomplexes [J].
Acin-Perez, Rebeca ;
Fernandez-Silva, Patricio ;
Luisa Peleato, Maria ;
Perez-Martos, Acisclo ;
Enriquez, Jose Antonio .
MOLECULAR CELL, 2008, 32 (04) :529-539
[2]   OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 [J].
Alexander, C ;
Votruba, M ;
Pesch, UEA ;
Thiselton, DL ;
Mayer, S ;
Moore, A ;
Rodriguez, M ;
Kellner, U ;
Leo-Kottler, B ;
Auburger, G ;
Bhattacharya, SS ;
Wissinger, B .
NATURE GENETICS, 2000, 26 (02) :211-215
[3]   Proteomic analysis of pharmacological preconditioning -: Novel protein targets converge to mitochondrial metabolism pathways [J].
Arrell, D. Kent ;
Elliott, Steven T. ;
Kane, Lesley A. ;
Guo, Yurong ;
Ko, Young H. ;
Pedersen, Pete L. ;
Robinson, John ;
Murata, Mitsushige ;
Murphy, Anne M. ;
Marban, Eduardo ;
Van Eyk, Jennifer E. .
CIRCULATION RESEARCH, 2006, 99 (07) :706-714
[4]   EFFECT OF HYPOXIA ON DEGRADATION OF MITOCHONDRIAL COMPONENTS IN RAT CARDIAC MUSCLE [J].
ASCHENBRENNER, V ;
ZAK, R ;
CUTILLETTA, AF ;
RABINOWITZ, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1971, 221 (05) :1418-+
[5]  
BEATTIE DS, 1967, J BIOL CHEM, V242, P4584
[6]   The role of autophagy in aging - Its essential part in the anti-aging mechanism of caloric restriction [J].
Bergamini, Ettore ;
Cavallini, Gabriella ;
Donati, Alessio ;
Gori, Zina .
HEALTHY AGING AND LONGEVITY, 2007, 1114 :69-78
[7]   Bcl-xL increases mitochondrial fission, fusion, and biomass in neurons [J].
Berman, Sarah B. ;
Chen, Ying-bei ;
Qi, Bing ;
McCaffery, J. Michael ;
Rucker, Edmund B., III ;
Goebbels, Sandra ;
Nave, Klaus-Armin ;
Arnold, Beth A. ;
Jonas, Elizabeth A. ;
Pineda, Fernando J. ;
Hardwick, J. Marie .
JOURNAL OF CELL BIOLOGY, 2009, 184 (05) :707-719
[8]   Cyclophilin D is required for mitochondrial removal by autophagy in cardiac cells [J].
Carreira, Raquel S. ;
Lee, Youngil ;
Ghochani, Mariam ;
Gustafsson, Asa B. ;
Gottlieb, Roberta A. .
AUTOPHAGY, 2010, 6 (04) :462-472
[9]   Nix and Nip3 form a subfamily of pro-apoptotic mitochondrial proteins [J].
Chen, G ;
Cizeau, J ;
Velde, CV ;
Park, JH ;
Bozek, G ;
Bolton, J ;
Shi, L ;
Dubik, D ;
Greenberg, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (01) :7-10
[10]   Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development [J].
Chen, HC ;
Detmer, SA ;
Ewald, AJ ;
Griffin, EE ;
Fraser, SE ;
Chan, DC .
JOURNAL OF CELL BIOLOGY, 2003, 160 (02) :189-200