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A Serpin Shapes the Extracellular Environment to Prevent Influenza A Virus Maturation

机译:丝氨酸蛋白酶抑制剂塑造细胞外环境,以防止甲型流感病毒成熟

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Interferon-stimulated genes (ISGs) act in concert to provide a tight barrier against viruses. Recent studies have shed light on the contribution of individual ISG effectors to the antiviral state, but most have examined those acting on early, intracellular stages of the viral life cycle. Here, we applied an image-based screen to identify ISGs inhibiting late stages of influenza A virus (IAV) infection. We unraveled a directly antiviral function for the gene SERPINE1, encoding plasminogen activator inhibitor 1 (PAI-1). By targeting extracellular airway proteases, PAI-1 inhibits IAV glycoprotein cleavage, thereby reducing infectivity of progeny viruses. This was biologically relevant for IAV restriction in vivo. Further, partial PAI-1 deficiency, attributable to a polymorphism in human SERPINE1, conferred increased susceptibility to IAV in vitro. Together, our findings reveal that manipulating the extracellular environment to inhibit the last step in a virus life cycle is an important mechanism of the antiviral response.
机译:干扰素刺激基因(ISG)共同发挥作用,为病毒提供了严密的屏障。最近的研究揭示了单个ISG效应物对抗病毒状态的贡献,但大多数研究人员检查了那些在病毒生命周期的早期,细胞内阶段起作用的物质。在这里,我们应用了基于图像的屏幕来识别ISG抑制甲型流感病毒(IAV)感染后期。我们揭示了SERPINE1基因的直接抗病毒功能,该基因编码纤溶酶原激活物抑制剂1(PAI-1)。通过靶向细胞外气道蛋白酶,PAI-1抑制了IAV糖蛋白的裂解,从而降低了子代病毒的感染性。这与体内IAV限制生物学相关。此外,可归因于人SERPINE1基因多态性的部分PAI-1缺乏症使体外对IAV的敏感性增加。总之,我们的发现表明,操纵细胞外环境抑制病毒生命周期的最后一步是抗病毒反应的重要机制。

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