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肠道病毒 71 通过 COX-2/PGE2/cAMP 依赖途径调节人神经母细胞瘤细胞内病毒复制:c-Src/EGFR/p42/p44 MAPK/CREB 信号通路的作用。

Enterovirus 71 modulates a COX-2/PGE2/cAMP-dependent viral replication in human neuroblastoma cells: role of the c-Src/EGFR/p42/p44 MAPK/CREB signaling pathway.

机构信息

Department of Physiology and Pharmacology, Chang Gung University, Kwei-San, Tao-Yuan, Taiwan.

出版信息

J Cell Biochem. 2011 Feb;112(2):559-70. doi: 10.1002/jcb.22946.

Abstract

Enterovirus 71 (EV71) has been shown to induce cyclooxygenase-2 (COX-2) expression in human neuroblastoma SK-N-SH cells through the action of MAPKs, NF-κB, and AP-1. On the other hand, the transcription factor CREB has also been implicated in the expression of COX-2 in other cell lines. Here, we report that EV71-induced COX-2 expression and PGE(2) production were both inhibited by pretreatment with the PKA inhibitor H89 or by transfection with CREB siRNA. In addition, EV71-induced COX-2 expression and c-Src/EGFR phosphorylation were both attenuated by transfection with c-Src siRNA or pretreatment with the inhibitors of c-Src (PP1) or EGF receptor (EGFR) (AG1478 and EGFR-neutralizing antibody). We also observed that EV71-induced p42/p44 MAPK phosphorylation was decreased following pretreatment with AG1478. Moreover, EV71-induced COX-2 expression was blocked by pretreatment with the p300 inhibitor GR343 or by transfection with p300 siRNA. Using immunoprecipitation and chromatin immunoprecipitation assays, we observed that EV71 stimulated the association of CREB and p300 with the COX-2 promoter region. Notably, we also demonstrated that EV71-induced COX-2 expression and PGE(2) production promoted viral replication via cAMP signaling. In summary, this study demonstrates that EV71 activates the c-Src/EGFR/p42/p44 MAPK pathway in human SK-N-SH cell, which leads to the activation of CREB/p300, and stimulates COX-2 expression and PGE(2) release.

摘要

肠道病毒 71(EV71)已被证明通过 MAPKs、NF-κB 和 AP-1 的作用诱导人神经母细胞瘤 SK-N-SH 细胞中环氧化酶-2(COX-2)的表达。另一方面,转录因子 CREB 也被牵连到其他细胞系中 COX-2 的表达。在这里,我们报告 EV71 诱导的 COX-2 表达和 PGE(2)的产生都被 PKA 抑制剂 H89 的预处理或 CREB siRNA 的转染所抑制。此外,EV71 诱导的 COX-2 表达和 c-Src/EGFR 磷酸化都被 c-Src siRNA 的转染或 c-Src(PP1)或 EGF 受体(EGFR)抑制剂(AG1478 和 EGFR 中和抗体)的预处理所减弱。我们还观察到,AG1478 预处理后,EV71 诱导的 p42/p44 MAPK 磷酸化减少。此外,EV71 诱导的 COX-2 表达被 p300 抑制剂 GR343 的预处理或 p300 siRNA 的转染所阻断。通过免疫沉淀和染色质免疫沉淀实验,我们观察到 EV71 刺激 CREB 和 p300 与 COX-2 启动子区域的结合。值得注意的是,我们还证明 EV71 诱导的 COX-2 表达和 PGE(2)的产生通过 cAMP 信号促进病毒复制。总之,本研究表明,EV71 在人 SK-N-SH 细胞中激活 c-Src/EGFR/p42/p44 MAPK 通路,导致 CREB/p300 的激活,并刺激 COX-2 的表达和 PGE(2)的释放。

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