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Reciprocal Regulation of AKT and MAP Kinase Dictates Virus-Host Cell Fusion

机译:AKT和MAP激酶的相互调节决定了病毒-宿主细胞融合

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摘要

Viruses of the Paramyxoviridae family bind to their host cells by using hemagglutinin-neuraminidase (HN), which enhances fusion protein (F)-mediated membrane fusion. Although respiratory syncytial virus and parainfluenza virus 5 of this family are suggested to trigger host cell signaling during infection, the virus-induced intracellular signals dictating virus-cell fusion await elucidation. Using an F- or HN-F-containing reconstituted envelope of Sendai virus, another paramyxovirus, we revealed the role and regulation of AKT1 and Raf/MEK/ERK cascades during viral fusion with liver cells. Our observation that extracellular signal-regulated kinase (ERK) activation promotes viral fusion via ezrin-mediated cytoskeletal rearrangements, whereas AKT1 attenuates fusion by promoting phosphorylation of F protein, indicates a counteractive regulation of viral fusion by reciprocal activation of AKT1 and mitogen-activated protein kinase (MAPK) cascades, establishing a novel conceptual framework for a therapeutic strategy.
机译:副粘病毒科的病毒通过使用血凝素神经氨酸酶(HN)与它们的宿主细胞结合,从而增强融合蛋白(F)介导的膜融合。尽管建议该家族的呼吸道合胞病毒和副流感病毒5在感染过程中触发宿主细胞信号传导,但病毒诱导的指示病毒细胞融合的细胞内信号尚待阐明。使用含有F-或HN-F的仙台病毒(另一种副粘病毒)的重组包膜,我们揭示了在与肝细胞病毒融合过程中AKT1和Raf / MEK / ERK级联的作用和调控。我们的观察表明,细胞外信号调节激酶(ERK)激活通过ezrin介导的细胞骨架重排促进病毒融合,而AKT1通过促进F蛋白的磷酸化来减弱融合,这表明通过AKT1和促分裂原激活蛋白的相互激活,病毒融合具有反活性激酶(MAPK)级联,为治疗策略建立了新颖的概念框架。

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