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Transcription Factor CHF1/Hey2 Regulates Specific Pathways in Serum Stimulated Primary Cardiac Myocytes: Implications for Cardiac Hypertrophy

机译:转录因子CHF1 / Hey2调节血清刺激的原代心肌细胞的特定途径:对心脏肥大的影响。

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摘要

We have previously found that overexpression of CHF1/Hey2 in the myocardium prevents the development of phenylephrine-induced hypertrophy. To identify transcriptional pathways regulated by CHF1/Hey2, we cultured primary neonatal mouse cardiac myocytes from wild type and transgenic mice overexpressing CHF1/Hey2 and treated them with serum, a potent hypertrophic stimulus. We verified that overexpression of CHF1/Hey2 suppressed cardiac myocyte hypertrophy induced by serum and then determined transcriptional profiles by microarray hybridization. We identified and verified important downstream target genes by single gene analysis and qRT-PCR and then identified important biological processes by Gene Set Analysis using Biological Process Gene Sets from the Gene Ontology Consortium. We found that CHF1/Hey2 suppresses pathways involved in water transport, adenylate cyclase activity, embryonic eye morphogenesis, gut development and fluid transport after serum stimulation. Genes involved in protein dephosphorylation, demonstrate increased expression in myocytes overexpressing CHF1/Hey2, independent of serum treatment. Genes overexpressed prior to serum treatment are involved in regulation of transcription factor activity, nuclear protein export and steroid hormone receptor signaling. Genes overexpressed after serum treatment are involved in autophagy, apoptosis and mitochondrial biogenesis.
机译:我们以前已经发现,CHF1 / Hey2在心肌中的过度表达可防止苯肾上腺素引起的肥大的发展。为了鉴定受CHF1 / Hey2调控的转录途径,我们从野生型和过表达CHF1 / Hey2的转基因小鼠中培养了原代新生小鼠心脏心肌细胞,并用血清(一种有效的肥大刺激)对其进行了处理。我们验证了CHF1 / Hey2的过表达抑制了血清诱导的心肌肥大,然后通过微阵列杂交确定了转录谱。我们通过单基因分析和qRT-PCR鉴定并验证了重要的下游靶基因,然后使用来自基因本体联盟的生物过程基因组通过基因组分析鉴定了重要的生物学过程。我们发现CHF1 / Hey2抑制血清刺激后参与水运输,腺苷酸环化酶活性,胚胎眼形态发生,肠道发育和液体运输的途径。参与蛋白质去磷酸化的基因,在过表达CHF1 / Hey2的心肌细胞中表达增加,而与血清处理无关。血清治疗前过表达的基因参与转录因子活性,核蛋白输出和类固醇激素受体信号传导的调节。血清处理后过表达的基因参与自噬,细胞凋亡和线粒体生物发生。

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