American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · 2015 · 36 citations · 47 references
Life SciencesEndocrinologyMolecular GeneticsCell SignalingPediatric CardiologySignal TransductionCardiovascular DevelopmentCardiovascular Molecular PhysiologyGrowth Factor SignalingHeart DevelopmentCardiac Hypertrophy SignalingHeterotrimeric G Protein SignalingHistone Acetylation ProfilingHistone Acetylation VariationHistone-lysine AcetylationInsulin-like Growth Factors
The cardiac insulin-like growth factor 2 receptor (IGF-2R) can induce cardiomyocyte hypertrophy in a heterotrimeric G protein receptor-coupled manner involving αq (Gαq) or αs (Gαs). We have previously shown increased left ventricular weight and cardiac IGF-2 and IGF-2R gene expression in low-birth-weight (LBW) compared with average-birth-weight (ABW) lambs. Here, we have investigated the cardiac expression of IGF-2 gene variants, the degree of histone acetylation, and the abundance of proteins in the IGF-2R downstream signaling pathway in ABW and LBW lambs. Samples from the left ventricle of ABW and LBW lambs were collected at 21 days of age. There was increased phospho-CaMKII protein with decreased HDAC 4 abundance in the LBW compared with ABW lambs. There was increased GATA 4 and decreased phospho-troponin I abundance in LBW compared with ABW lambs, which are markers of pathological cardiac hypertrophy and impaired or reduced contractility, respectively. There was increased histone acetylation of H3K9 at IGF-2R promoter and IGF-2R intron 2 differentially methylated region in the LBW lamb. In conclusion, histone acetylation of IGF-2R may lead to increased IGF-2R mRNA expression and subsequently mediate Gαq signaling early in life via CaMKII, resulting in an increased risk of left ventricular hypertrophy and cardiovascular disease in adult life.
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Class II Histone Deacetylases Act as Signal-Responsive Repressors of Cardiac Hypertrophy
Chun Li Zhang, Timothy A. McKinsey, Shurong Chang et al. · Cell · 2002 · 979 citations · Full text