期刊
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
卷 46, 期 2, 页码 201-212出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.yjmcc.2008.10.025
关键词
Heart failure; Mitochondria; Fatty acid oxidation; PGC-1 alpha; ERR alpha; Raf-1; ERK; LCAD; Gene expression profiling
资金
- Genomics of Cardiovascular Development, Adaptation, and Remodeling, NHLBI Program
- N.I.H. [KO8 AG024844, 1K01HL088708-01]
- Alpha Omega Alpha Medical Student Research Fellowship
- N.I.H. Specialized Center for Clinically-Oriented Research (SCCOR) in Cardiac Dysfunction and Disease [P50 HL077113, 5P60 DK20579]
Heart failure is a cause of significant morbidity and mortality in developed nations, and results from a complex interplay between genetic and environmental factors. To discover gene regulatory networks underlying heart failure, we analyzed DNA microarray data based on left ventricular free-wall myocardium from 59 failing (32 ischemic cardiomyopathy, 27 idiopathic dilated cardiomyopathy) and 33 non-failing explanted human hearts from the Cardiogenomics Consortium. In particular, we sought to investigate cardiac gene expression changes at the level of individual genes, as well as biological pathways which contain groups of functionally related genes. Utilizing a combination of computational techniques, including Comparative Marker Selection and Gene Set Enrichment Analysis, we identified a subset of downstream gene targets of the master mitochondrial transcriptional regulator, peroxisome proliferator-activated receptor gamma coactivator-lot (PGC-1 alpha), whose expression is collectively decreased in failing human hearts. We also observed decreased expression of the key PGC-1 alpha regulatory partner, estrogen-related receptor alpha (ERR alpha). as well as ERR alpha target genes which may participate in the downregulation of mitochondrial metabolic capacity. Gene expression of the antiapoptotic Raf-1/extracellular signal-regulated kinase (ERK) pathway was decreased in failing hearts. Alterations in PGC-1 alpha and ERR alpha target gene sets were significantly correlated with an important clinical parameter of disease severity - left ventricular ejection fraction, and were predictive of failing vs. non-failing phenotypes. Overall, our results implicate PGC-1 alpha and ERR alpha in the pathophysiology of human heart failure, and define dynamic target gene sets sharing known interrelated regulatory mechanisms capable of contributing to the mitochondrial dysfunction characteristic of this disease process. (C) 2008 Elsevier Inc. All rights reserved.
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