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蛋白激酶C而非酪氨酸激酶或Ras,在心肌细胞中血管紧张素II诱导的Raf-1激酶激活和细胞外信号调节蛋白激酶激活过程中起关键作用。

Protein kinase C, but not tyrosine kinases or Ras, plays a critical role in angiotensin II-induced activation of Raf-1 kinase and extracellular signal-regulated protein kinases in cardiac myocytes.

作者信息

Zou Y, Komuro I, Yamazaki T, Aikawa R, Kudoh S, Shiojima I, Hiroi Y, Mizuno T, Yazaki Y

机构信息

Department of Medicine III, University of Tokyo School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113, Japan.

出版信息

J Biol Chem. 1996 Dec 27;271(52):33592-7. doi: 10.1074/jbc.271.52.33592.

Abstract

Angiotensin II (AngII) induces cardiac hypertrophy through activating a variety of protein kinases. In this study, to understand how cardiac hypertrophy develops, we examined AngII-evoked signal transduction pathways leading to the activation of extracellular signal-regulated protein kinases (ERKs), which are reportedly critical for the development of cardiac hypertrophy, in cultured cardiac myocytes isolated from neonatal rats. Inhibition of protein kinase C (PKC) with calphostin C or down-regulation of PKC by pretreatment with a phorbol ester for 24 h abolished AngII-induced activation of Raf-1 and ERKs, and addition of a phorbol ester conversely induced a marked increase in the activities of Raf-1 and ERKs. Pretreatment with two chemically and mechanistically dissimilar tyrosine kinase inhibitors, genistein and tyrphostin, did not attenuate AngII-induced activation of ERKs. In contrast, genistein strongly blocked insulin-induced ERK activation in cardiac myocytes. Although pretreatment with manumycin, a Ras farnesyltransferase inhibitor, or overexpression of a dominant-negative mutant of Ras inhibited insulin-induced ERK activation, neither affected AngII-induced activation of ERKs. Overexpression of a dominant-negative mutant of Raf-1 completely suppressed ERK2 activation by AngII, endothelin-1, and insulin. These results suggest that PKC and Raf-1, but not tyrosine kinases or Ras, are critical for AngII-induced activation of ERKs in cardiac myocytes.

摘要

血管紧张素II(AngII)通过激活多种蛋白激酶诱导心肌肥大。在本研究中,为了解心肌肥大的发生机制,我们检测了从新生大鼠分离的培养心肌细胞中,AngII引发的导致细胞外信号调节蛋白激酶(ERKs)激活的信号转导途径,据报道,ERKs对心肌肥大的发生至关重要。用钙泊三醇C抑制蛋白激酶C(PKC)或用佛波酯预处理24小时下调PKC,可消除AngII诱导的Raf-1和ERKs激活,相反,添加佛波酯可显著增加Raf-1和ERKs的活性。用两种化学和作用机制不同的酪氨酸激酶抑制剂染料木黄酮和 tyrphostin预处理,并未减弱AngII诱导的ERKs激活。相反,染料木黄酮强烈阻断胰岛素诱导的心肌细胞中ERK激活。虽然用Ras法尼基转移酶抑制剂曼诺霉素预处理或过表达Ras的显性负性突变体可抑制胰岛素诱导的ERK激活,但两者均不影响AngII诱导的ERKs激活。过表达Raf-1的显性负性突变体可完全抑制AngII、内皮素-1和胰岛素诱导的ERK2激活。这些结果表明,PKC和Raf-1而非酪氨酸激酶或Ras,对AngII诱导的心肌细胞中ERKs激活至关重要。

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