

Author: Alexandrov A. Keffel S. Goepel M. Michel M.C.
Publisher: Elsevier
ISSN: 0006-291X
Source: Biochemical and Biophysical Research Communications, Vol.261, Iss.2, 1999-08, pp. : 372-376
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
We have investigated the α1A-adrenoceptor-mediated activation of 46 and 54 kDa isoforms of c-jun N-terminal kinase (JNK) and of p38 mitogen-activated protein kinase. The α1-adrenoceptor agonist phenylephrine activated all three kinases but with different time courses and maximal effects. Activation of all three kinases was insensitive to the phosphatidylinositol-3-kinase inhibitor wortmannin but was enhanced by the protein kinase C inhibitor bisindolylmaleimide I; a protein kinase C-activating phorbol ester inhibited JNK but not p38 activation. Activation of 54 kDa JNK, but not of the other two kinases, was inhibited by pertussis toxin and the phospholipase C inhibitor U 73,122. We conclude that α1-adrenoceptor stimulation activates 46 kDa JNK, 54 kDa JNK and p38 but uses at least partly different pathways to do so.
Related content


By Yamauchi J. Itoh H. Shinoura H. Miyamoto Y. Hirasawa A. Kaziro Y. Tsujimoto G.
Biochemical and Biophysical Research Communications, Vol. 281, Iss. 4, 2001-03 ,pp. :


By Sopontammarak Somkiat Aliharoob Assad Ocampo Catherina Arcilla Rene Gupta Mahesh Gupta Madhu
Cell Biochemistry and Biophysics, Vol. 43, Iss. 1, 2005-02 ,pp. :


By Yamauchi J. Itoh H. Shinoura H. Miyamoto Y. Tsumaya K. Hirasawa A. Kaziro Y. Tsujimoto G.
Biochemical and Biophysical Research Communications, Vol. 288, Iss. 5, 2001-11 ,pp. :




By Wang Feng-Ming Hu Tao Tan Hong Zhou Xue-Dong
Molecular and Cellular Biochemistry, Vol. 291, Iss. 1-2, 2006-10 ,pp. :