Wu B, Wang T H, Zhu X N, Pan J Y
Department of Physiology, Sun Yat-Sen University of Medical Sciences, Guangzhou 510089.
Sheng Li Xue Bao. 1999 Feb;51(1):19-24.
In the present study, the effect of endothelin-1 (ET-1) on the expression of proto-oncogene c-fos in cultured neonatal rat myocardial cells was investigated. The results are as follows: ET-1 induced c-fos expression in a dose-dependent manner. Selective ET(A) receptor antagonist blocked ET-1-induced responses. Protein kinase C(PKC) agonist PMA induced c-fos expression.PKC inhibitor staurosporine blocked ET-1 induced c-fos expression. Calcium channel blocker, nifedipine did not significantly affect the expression of c-fos induced by ET-1. These results suggest that in cultured neonatal cardiomyocytes, ET-1 induced c-fos gene expression is mediated by ET(A) receptor with the participation of protein kinase C, while the voltage-dependent L-type Ca(2+) channel is not involved.
在本研究中,研究了内皮素-1(ET-1)对培养的新生大鼠心肌细胞中原癌基因c-fos表达的影响。结果如下:ET-1以剂量依赖性方式诱导c-fos表达。选择性ET(A)受体拮抗剂阻断了ET-1诱导的反应。蛋白激酶C(PKC)激动剂PMA诱导c-fos表达。PKC抑制剂星形孢菌素阻断了ET-1诱导的c-fos表达。钙通道阻滞剂硝苯地平对ET-1诱导的c-fos表达没有显著影响。这些结果表明,在培养的新生心肌细胞中,ET-1诱导的c-fos基因表达是由ET(A)受体介导的,蛋白激酶C参与其中,而电压依赖性L型Ca(2+)通道不参与。