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组成性激活的 Ras 通过诱导 NIH3T3 细胞中的 MAP 激酶磷酸酶 3(MKP3)负调控 Erk MAP 激酶。

Constitutively active Ras negatively regulates Erk MAP kinase through induction of MAP kinase phosphatase 3 (MKP3) in NIH3T3 cells.

机构信息

Laboratory of Immunobiology, School of Life Science and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu 702-701, Korea.

Department of Biological Sciences, College of Biological Science and Biotechnology, Konkuk University, Seoul 143-701, Korea.

出版信息

BMB Rep. 2014 Dec;47(12):685-90. doi: 10.5483/bmbrep.2014.47.12.017.

Abstract

The Ras/Raf/MEK/Erk signaling pathway is important for regulation of cell growth, proliferation, differentiation, survival, and apoptosis in response to a variety of extracellular stimuli. Lack of Erk MAPK activation is observed in several cancer cells despite active activation of Ras. However, little is known about the modulation of Erk1/2 activity by active Ras. Here, we show that overexpression of active H-Ras (H-RasG12R) in NIH3T3 fibroblasts impaired FGF2-induced Erk1/2 phosphorylation, as compared to wild-type cells. Northern blot analysis revealed that prolonged expression of active Ras increased MAP kinase phosphatase 3 (MKP3) mRNA expression, a negative regulator of Erk MAPK. Inhibition of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway abrogated active Ras-induced up-regulation of MKP3 expression, leading to the rescue of Erk1/2 phosphorylation. Our results demonstrated that the Ras/Raf/MEK/Erk signaling cascade is negatively regulated by the PI3K/Akt dependent transcriptional activation of the MKP3 gene.

摘要

Ras/Raf/MEK/Erk 信号通路对于细胞生长、增殖、分化、存活和凋亡的调节非常重要,它可以对各种细胞外刺激做出反应。尽管 Ras 处于激活状态,但在一些癌细胞中观察到 Erk MAPK 的激活缺失。然而,关于活性 Ras 对 Erk1/2 活性的调节,人们知之甚少。在这里,我们发现与野生型细胞相比,NIH3T3 成纤维细胞中活性 H-Ras(H-RasG12R)的过表达会损害 FGF2 诱导的 Erk1/2 磷酸化。Northern blot 分析显示,活性 Ras 的长期表达会增加 MAP 激酶磷酸酶 3(MKP3)mRNA 的表达,MKP3 是 Erk MAPK 的负调控因子。PI3K/Akt 通路的抑制消除了活性 Ras 诱导的 MKP3 表达上调,导致 Erk1/2 磷酸化的恢复。我们的结果表明,Ras/Raf/MEK/Erk 信号级联通过 PI3K/Akt 依赖性转录激活 MKP3 基因来负调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2b/4345513/2cad0e515da7/BMB-47-685-g001.jpg

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