Department of Biochemistry, University of Delhi South Campus, Benito Juarez Road, New Delhi 110021, India.
J Virol. 2010 May;84(9):4366-82. doi: 10.1128/JVI.01940-09. Epub 2010 Feb 17.
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.
副粘病毒家族的病毒通过使用血凝素神经氨酸酶(HN)与宿主细胞结合,从而增强融合蛋白(F)介导的膜融合。尽管该家族的呼吸道合胞病毒和副流感病毒 5 被认为在感染过程中触发宿主细胞信号转导,但决定病毒-细胞融合的病毒诱导的细胞内信号仍有待阐明。我们使用另一种副粘病毒仙台病毒的含有 F 或 HN-F 的重建包膜,揭示了 AKT1 和 Raf/MEK/ERK 级联在与肝细胞融合过程中的作用和调节。我们的观察结果表明,细胞外信号调节激酶(ERK)的激活通过 ezrin 介导的细胞骨架重排促进病毒融合,而 AKT1 通过促进 F 蛋白的磷酸化来抑制融合,这表明 AKT1 和丝裂原活化蛋白激酶(MAPK)级联的相互激活对病毒融合进行拮抗调节,为治疗策略建立了一个新的概念框架。