The p38 pathway regulates Akt both at the protein and transcriptional activation levels during myogenesis

被引:49
作者
Cabane, C
Coldefy, AS
Yeow, K
Dérijard, B
机构
[1] Univ Nice, Fac Sci, Lab Physiol Cellulaire & Mol, CNRS,UMR 6548, F-06108 Nice, France
[2] Serono Int SA, CH-1211 Geneva 20, Switzerland
关键词
p38; MAPK; Akt; signalling; myogenesis; muscle cell differentiation;
D O I
10.1016/j.cellsig.2004.05.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The molecular signalling pathways governing skeletal muscle differentiation remain unclear. Recent work has demonstrated that both the phosphatidylinositol 3-kinase (PI3K)/Akt and p38 pathways play important roles in myogenesis. Here, we describe the interactions between these pathways in C2C12 cells. Overall, our results suggest that Akt acts downstream of p38 in myogenic cell differentiation. Activating the p38 pathway results in the concurrent activation of Akt; conversely, activating Akt does not affect p38. We have analysed Akt messenger RNA and protein levels in a C2C12 cell line stably expressing a dominant negative (DN) form of the p38 activator MKK3. Compared to control cells, this cell line exhibits reduced levels of Akt messenger RNA and total protein. In addition, blocking the p38 pathway during differentiation inhibits Akt activation. Our results show for the first time that p38 can directly affect Akt at the transcriptional level as well as at the protein activation level during myogenic differentiation. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1405 / 1415
页数:11
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