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Selective unresponsiveness to the inhibition of p38 MAPK activation by cAMP helps L929 fibroblastoma cells escape TNF-α-induced cell death

机译:对cAMP抑制p38 MAPK激活的选择性无反应性有助于L929成纤维细胞瘤细胞逃脱TNF-α诱导的细胞死亡

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摘要

BackgroundThe cyclic AMP (cAMP) signaling pathway has been reported to either promote or suppress cell death, in a cell context-dependent manner. Our previous study has shown that the induction of dynein light chain (DLC) by cAMP response element-binding protein (CREB) is required for cAMP-mediated inhibition of mitogen-activated protein kinase (MAPK) p38 activation in fibroblasts, which leads to suppression of NF-κB activity and promotion of tumor necrosis factor-α (TNF-α)-induced cell death. However, it remains unknown whether this regulation is also applicable to fibroblastoma cells.
机译:背景技术据报道,环状AMP(cAMP)信号通路以依赖于细胞背景的方式促进或抑制细胞死亡。我们以前的研究表明,cAMP响应元件结合蛋白(CREB)诱导动力蛋白轻链(DLC)是cAMP介导抑制成纤维细胞中促分裂原活化蛋白激酶(MAPK)p38激活的必需条件,导致抑制NF-κB活性和促进肿瘤坏死因子-α(TNF-α)诱导的细胞死亡的研究。然而,尚不清楚该调节是否也适用于成纤维细胞瘤细胞。

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