首页> 外文期刊>Life sciences >PROTEIN KINASES AND PHOSPHATASES MODULATE C-FOS EXPRESSION IN RAT HEPATOCYTES - EFFECTS OF ANGIOTENSIN II AND PHORBOL MYRISTATE ACETATE
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PROTEIN KINASES AND PHOSPHATASES MODULATE C-FOS EXPRESSION IN RAT HEPATOCYTES - EFFECTS OF ANGIOTENSIN II AND PHORBOL MYRISTATE ACETATE

机译:蛋白激酶和磷酸酶调节大鼠肝细胞中C-FOS的表达-血管紧张素II和醋酸乙酰苯酚的作用

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In isolated rat hepatocytes angiotensin II and phorbol 12-myristate 13-acetate(PMA) induce the expression of c-fos. We studied the possible transduction pathway(s) involved in this effect using inhibitors of serine-threonine and tyrosine protein kinases. Calphostin and staurosporine, inhibitors of protein kinase C and other serine-threonine protein kinases, block in a dose-dependent manner the effect of angiotensin II and PMA. Interestingly, genistein also blocks the induction of this proto-oncogene, suggesting a role for tyrosine protein kinases. Inhibitors of serine-threonine protein phosphatases, such as okadaic acid, microcystin LR and calyculin also induce c-fos expression. These data suggest that protein phosphatases exert a tonic inhibitory control of c-fos expression. The effect of these phosphatase inhibitors were not blocked by staurosporine, calphostin or genistein. Our results suggest that the expression of c-fos in rat hepatocytes is regulated by complex phosphorylation-dephosphorytation cascade(s) probably involving serine/threonine and tyrosine protein kinase and protein phosphatase activities. [References: 38]
机译:在分离的大鼠肝细胞中,血管紧张素II和佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)诱导c-fos的表达。我们使用丝氨酸-苏氨酸和酪氨酸蛋白激酶抑制剂研究了可能与这种作用有关的转导途径。 Calphostin和staurosporine,蛋白激酶C和其他丝氨酸-苏氨酸蛋白激酶的抑制剂,以剂量依赖的方式阻断血管紧张素II和PMA的作用。有趣的是,染料木黄酮还可以阻止这种原癌基因的诱导,提示酪氨酸蛋白激酶的作用。丝氨酸-苏氨酸蛋白磷酸酶的抑制剂,例如冈田酸,微囊藻毒素LR和钙霉素也诱导c-fos表达。这些数据表明蛋白质磷酸酶发挥了对c-fos表达的抑制作用。这些磷酸酶抑制剂的作用不会被星形孢菌素,钙磷蛋白或染料木黄酮所阻断。我们的结果表明,大鼠肝细胞中c-fos的表达受复杂的磷酸化-去磷酸化级联反应的调节,可能涉及丝氨酸/苏氨酸和酪氨酸蛋白激酶以及蛋白磷酸酶的活性。 [参考:38]

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