Maintaining Ancient Organelles Mitochondrial Biogenesis and Maturation

被引:114
作者
Vega, Rick B. [1 ]
Horton, Julie L. [1 ]
Kelly, Daniel P. [1 ]
机构
[1] Sanford Burnham Med Res Inst Lake Nona, Diabet & Obes Res Ctr, Cardiovasc Pathobiol Program, Orlando, FL 32827 USA
基金
美国国家卫生研究院;
关键词
mitochondria; mitochondrial turnover; myocytes; cardiac; oxidative phosphorylation; transcription factors; PROLIFERATOR-ACTIVATED-RECEPTOR; FATTY-ACID OXIDATION; CYTOCHROME-C-OXIDASE; DNA-BINDING PROTEIN; ALPHA PPAR-ALPHA; TRANSCRIPTIONAL COACTIVATOR PGC-1; PALMITOYLTRANSFERASE I GENE; CARDIAC HYPERTROPHIC GROWTH; NUCLEAR RESPIRATORY FACTORS; COMPLEX-I;
D O I
10.1161/CIRCRESAHA.116.305420
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ultrastructure of the cardiac myocyte is remarkable for the high density of mitochondria tightly packed between sarcomeres. This structural organization is designed to provide energy in the form of ATP to fuel normal pump function of the heart. A complex system comprised of regulatory factors and energy metabolic machinery, encoded by both mitochondrial and nuclear genomes, is required for the coordinate control of cardiac mitochondrial biogenesis, maturation, and high-capacity function. This process involves the action of a transcriptional regulatory network that builds and maintains the mitochondrial genome and drives the expression of the energy transduction machinery. This finely tuned system is responsive to developmental and physiological cues, as well as changes in fuel substrate availability. Deficiency of components critical for mitochondrial energy production frequently manifests as a cardiomyopathic phenotype, underscoring the requirement to maintain high respiration rates in the heart. Although a precise causative role is not clear, there is increasing evidence that perturbations in this regulatory system occur in the hypertrophied and failing heart. This review summarizes current knowledge and highlights recent advances in our understanding of the transcriptional regulatory factors and signaling networks that serve to regulate mitochondrial biogenesis and function in the mammalian heart.
引用
收藏
页码:1820 / 1834
页数:15
相关论文
共 183 条
[1]   Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy [J].
Abdulhag, Ulla Najwa ;
Soiferman, Devorah ;
Schueler-Furman, Ora ;
Miller, Chaya ;
Shaag, Avraham ;
Elpeleg, Orly ;
Edvardson, Simon ;
Saada, Ann .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (02) :159-164
[2]   Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria [J].
Acehan, Devrim ;
Malhotra, Ashim ;
Xu, Yang ;
Ren, Mindong ;
Stokes, David L. ;
Schlame, Michael .
BIOPHYSICAL JOURNAL, 2011, 100 (09) :2184-2192
[3]   Replication-transcription switch in human mitochondria [J].
Agaronyan, Karen ;
Morozov, Yaroslav I. ;
Anikin, Michael ;
Temiakov, Dmitry .
SCIENCE, 2015, 347 (6221) :548-551
[4]   Myc controls transcriptional regulation of cardiac metabolism and mitochondrial biogenesis in response to pathological stress in mice [J].
Ahuja, Preeti ;
Zhao, Peng ;
Angelis, Ekaterini ;
Ruan, Hongmei ;
Korge, Paavo ;
Olson, Aaron ;
Wang, Yibin ;
Jin, Eunsook S. ;
Jeffrey, F. Mark ;
Portman, Michael ;
MacLellan, W. Robb .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (05) :1494-1505
[5]   ERRγ directs and maintains the transition to oxidative metabolism in the postnatal heart [J].
Alaynick, William A. ;
Kondo, Richard P. ;
Xie, Wen ;
He, Weimin ;
Dufour, Catherine R. ;
Downes, Michael ;
Jonker, Johan W. ;
Giles, Wayne ;
Naviaux, Robert K. ;
Giguere, Vincent ;
Evans, Ronald M. .
CELL METABOLISM, 2007, 6 (01) :13-24
[6]   Mitochondrial transcription is regulated via an ATP "sensing" mechanism that couples RNA abundance to respiration [J].
Amiott, Elizabeth A. ;
Jaehning, Judith A. .
MOLECULAR CELL, 2006, 22 (03) :329-338
[7]   PGC-l-related coactivator, a novel, serum-inducible coactivator of nuclear respiratory factor 1-dependent transcription in mammalian cells [J].
Andersson, U ;
Scarpulla, RC .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (11) :3738-3749
[8]   A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy [J].
Andreu, AL ;
Checcarelli, N ;
Iwata, S ;
Shanske, S ;
DiMauro, S .
PEDIATRIC RESEARCH, 2000, 48 (03) :311-314
[9]  
ANTOSHECHKIN I, 1995, MOL CELL BIOL, V15, P7032
[10]   Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα) [J].
Aoyama, T ;
Peters, JM ;
Iritani, N ;
Nakajima, T ;
Furihata, K ;
Hashimoto, T ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5678-5684