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

机译:p38途径在成肌过程中在蛋白和转录激活水平上均调节Akt

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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.
机译:控制骨骼肌分化的分子信号传导途径仍不清楚。最近的工作表明,磷脂酰肌醇3-激酶(PI3K)/ Akt和p38途径均在肌发生中起重要作用。在这里,我们描述了C2C12细胞中这些途径之间的相互作用。总的来说,我们的结果表明Akt在成肌细胞分化中作用于p38的下游。激活p38途径导致同时激活Akt。相反,激活Akt不会影响p38。我们已经分析了稳定表达p38激活因子MKK3的显性负(DN)形式的C2C12细胞系中的Akt信使RNA和蛋白质水平。与对照细胞相比,该细胞系显示出降低的Akt信使RNA和总蛋白水平。此外,在分化过程中阻断p38途径可抑制Akt激活。我们的结果首次表明,p38可以在成肌分化过程中直接在转录水平以及蛋白激活水平上影响Akt。 (C)2004 Elsevier Inc.保留所有权利。

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