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在肌生成过程中,p38信号通路在蛋白质和转录激活水平上均对Akt进行调控。

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

作者信息

Cabane Candice, Coldefy Anne-Sophie, Yeow Karen, Dérijard Benoît

机构信息

UMR CNRS 6548, Laboratoire de Physiologie Cellulaire et Moléculaire, Université de Nice-Sophia Antipolis, Faculté des Sciences, 28 Avenue Valrose, 06108 Nice, France.

出版信息

Cell Signal. 2004 Dec;16(12):1405-15. doi: 10.1016/j.cellsig.2004.05.003.

Abstract

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.

摘要

调控骨骼肌分化的分子信号通路仍不清楚。最近的研究表明,磷脂酰肌醇3激酶(PI3K)/Akt和p38信号通路在肌生成过程中均发挥重要作用。在此,我们描述了C2C12细胞中这些信号通路之间的相互作用。总体而言,我们的结果表明,在肌源性细胞分化过程中,Akt在p38的下游发挥作用。激活p38信号通路会导致Akt同时被激活;相反,激活Akt并不影响p38。我们分析了稳定表达p38激活剂MKK3显性负性(DN)形式的C2C12细胞系中Akt信使核糖核酸(mRNA)和蛋白质水平。与对照细胞相比,该细胞系中Akt mRNA和总蛋白水平降低。此外,在分化过程中阻断p38信号通路会抑制Akt的激活。我们的结果首次表明,在肌源性分化过程中,p38可以在转录水平以及蛋白质激活水平直接影响Akt。

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