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

机译:组成型活性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

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摘要

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/Aktdependent transcriptional activation of the MKP3 gene. [BMB Reports 2014; 47(12): 685-690]
机译:Ras / Raf / MEK / Erk信号通路对于调节细胞生长,增殖,分化,存活和凋亡对多种细胞外刺激的反应都很重要。尽管Ras活跃激活,但仍在几个癌细胞中观察到Erk MAPK激活不足。然而,关于活性Ras对Erk1 / 2活性的调节知之甚少。在这里,我们显示与野生型细胞相比,NIH3T3成纤维细胞中活性H-Ras(H-RasG12R)的过表达损害了FGF2诱导的Erk1 / 2磷酸化。 Northern印迹分析表明,活性Ras的延长表达增加了MAP激酶磷酸酶3(MKP3)mRNA的表达,这是Erk MAPK的负调节剂。磷脂酰肌醇3激酶(PI3K)/ Akt途径的抑制废除了活性Ras诱导的MKP3表达的上调,从而挽救了Erk1 / 2磷酸化。我们的结果证明Ras / Raf / MEK / Erk信号级联受到MKP3基因的PI3K / Akt依赖性转录激活的负调控。 [BMB报告2014; 47(12):685-690]

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