Quantitative Phosphoproteomic Study of Pressure-Overloaded Mouse Heart Reveals Dynamin-Related Protein 1 as a Modulator of Cardiac Hypertrophy

Pressure-overload stress to the heart causes pathological cardiac hypertrophy, which increases the risk of cardiac morbidity and mortality. However, the detailed signaling pathways induced by pressure overload remain unclear. Here we used phosphoproteomics to delineate signaling pathways in the myoc...

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Bibliographic Details
Published in:Molecular & cellular proteomics 2013-11, Vol.12 (11), p.3094-3107
Main Authors: Chang, Yu-Wang, Chang, Ya-Ting, Wang, Qinchuan, Lin, Jim Jung-Ching, Chen, Yu-Ju, Chen, Chien-Chang
Format: Article
Language:English
Subjects:
Animals
Cardiomegaly - etiology
Cardiomegaly - metabolism
Cells, Cultured
Dynamins - chemistry
Dynamins - metabolism
Hypertrophy, Left Ventricular - etiology
Hypertrophy, Left Ventricular - metabolism
Male
Mice
Mice, Inbred C57BL
Myocytes, Cardiac - drug effects
Myocytes, Cardiac - metabolism
Myocytes, Cardiac - pathology
Oxygen Consumption - drug effects
Phenylephrine - pharmacology
Phosphorylation
Proteomics
Rats
Signal Transduction
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Summary:Pressure-overload stress to the heart causes pathological cardiac hypertrophy, which increases the risk of cardiac morbidity and mortality. However, the detailed signaling pathways induced by pressure overload remain unclear. Here we used phosphoproteomics to delineate signaling pathways in the myocardium responding to acute pressure overload and chronic hypertrophy in mice. Myocardial samples at 4 time points (10, 30, 60 min and 2 weeks) after transverse aortic banding (TAB) in mice underwent quantitative phosphoproteomics assay. Temporal phosphoproteomics profiles showed 360 phosphorylation sites with significant regulation after TAB. Multiple mechanical stress sensors were activated after acute pressure overload. Gene ontology analysis revealed differential phosphorylation between hearts with acute pressure overload and chronic hypertrophy. Most interestingly, analysis of the cardiac hypertrophy pathway revealed phosphorylation of the mitochondrial fission protein dynamin-related protein 1 (DRP1) by prohypertrophic kinases. Phosphorylation of DRP1 S622 was confirmed in TAB-treated mouse hearts and phenylephrine (PE)-treated rat neonatal cardiomyocytes. TAB-treated mouse hearts showed phosphorylation-mediated mitochondrial translocation of DRP1. Inhibition of DRP1 with the small-molecule inhibitor mdivi-1 reduced the TAB-induced hypertrophic responses. Mdivi-1 also prevented PE-induced hypertrophic growth and oxygen consumption in rat neonatal cardiomyocytes. We reveal the signaling responses of the heart to pressure stress in vivo and in vitro. DRP1 may be important in the development of cardiac hypertrophy.
ISSN:1535-9476
1535-9484
DOI:10.1074/mcp.M113.027649