Journal of proteome research · 2009
Alterations of mitochondrial enzymes contribute to cardiac hypertrophy before hypertension development in spontaneously hypertensive rats.
Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Meng Chao, Jin Xian, Xia Li, Shen Shao-Ming, Wang Xiao-Ling, Cai Jun, Chen Guo-Qiang, Wang Li-Shun, Fang Ning-Yuan
Аннотация
Mitochondrial dysfunction is recently thought to be tightly associated with the development of cardiac hypertrophy as well as hypertension. However, the detailed molecular events in mitochondria at early stages of hypertrophic pathogenesis are still unclear. Applying two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) combined with MALDI-TOF/TOF tandem mass spectrometry, here we identified the changed mitochondrial proteins of left ventricular mitochondria in prehypertensive/hypertensive stages of cardiac hypertrophy through comparing spontaneously hypertensive rats (SHR) and the age-matched normotensive Wistar Kyoto (WKY) rats. The results revealed that in the hypertrophic left ventricle of SHR as early as 4 weeks old with normal blood pressure, 33 mitochondrial protein spots presented significant alterations, with 17 down-regulated and 16 up-regulated. Such alterations were much greater than those in 20-week-old SHR with elevated blood pressure. Of the total alterations, the expression of two mitochondrial enzymes, trifunctional enzyme alpha subunit (Hadha) and NADH dehydrogenase 1 alpha subcomplex 10 (Ndufa10), were found to have special expression modification patterns in SHR strain. These data would provide new clues to investigate the potential contribution of mitochondrial dysfunction to the development of cardiac hypertrophy.
Предметные рубрики MeSH
3-Hydroxyacyl CoA DehydrogenasesAmino Acid SequenceAnimalsBase SequenceBlotting, WesternCardiomegalyDNA Mutational AnalysisElectrophoresis, Gel, Two-DimensionalGene Expression Regulation, EnzymologicHypertensionMaleMitochondria, HeartMitochondrial ProteinsModels, BiologicalMolecular Sequence DataMyocardiumNADH DehydrogenasePoint MutationProteomicsRatsRats, Inbred SHRRats, Inbred WKYReverse Transcriptase Polymerase Chain ReactionSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTime Factors