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Cardiac myocyte hypertrophy is associated with c-myc protooncogene expression.

机译:心肌心肌肥大与c-myc原癌基因表达有关。

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摘要

The mechanism of hormonally induced cell hypertrophy is unknown. Stimulation of cardiac myocytes by alpha 1-adrenergic agents, phorbol esters, and serum induces an increase in the cell size of nondividing cardiac myocytes in primary culture. Expression of the c-myc gene, known to be increased in growth factor-induced cell division, was studied in this model of cell hypertrophy. The alpha-adrenergic agonist norepinephrine (0.002-20 microM) increased levels of c-myc-encoded mRNA to 10-fold over control levels. This increase was detectable at 30 min, peaked at 2 hr, and returned to baseline by 6 hr after stimulation. The norepinephrine response was abolished by the alpha 1-antagonist terazosin (2 microM) but was not affected by the beta-adrenergic antagonist propranolol (2 microM) and was only slightly (25%) attenuated by the alpha 2-adrenergic antagonist yohimbine (2 microM). Serum and the phorbol ester tumor promoter phorbol 12-myristate 13-acetate also enhanced c-myc expression in cardiac myocyte cultures. These findings show that the induction of cardiac myocyte hypertrophy is associated with enhanced expression of the c-myc gene and suggest that hormonally induced cell hypertrophy and cell division share common mechanistic pathways.
机译:激素诱导的细胞肥大的机制尚不清楚。 α1-肾上腺素能药物,佛波醇酯和血清刺激心肌细胞会导致原代培养中未分裂的心肌细胞的细胞大小增加。在这种细胞肥大模型中研究了已知在生长因子诱导的细胞分裂中增加的c-myc基因的表达。 α-肾上腺素能激动剂去甲肾上腺素(0.002-20 microM)使c-myc编码的mRNA水平增加至对照水平的10倍。这种增加在30分钟时可检测到,在2小时达到峰值,并在刺激后6小时回到基线。去甲肾上腺素的反应被α1拮抗剂特拉唑嗪(2 microM)消除,但不受β-肾上腺素拮抗剂普萘洛尔(2 microM)的影响,而仅被α2-肾上腺素拮抗剂育亨宾(2)减弱(25%)。 microM)。血清和佛波醇酯肿瘤启动子佛波醇12-肉豆蔻酸酯13-乙酸酯还增强了心肌细胞培养物中c-myc的表达。这些发现表明,心肌细胞肥大的诱导与c-myc基因表达的增强有关,并且表明激素诱导的细胞肥大和细胞分裂共有共同的机制途径。

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