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干扰素诱导的LY6E蛋白促进HIV-1感染。

Interferon-inducible LY6E Protein Promotes HIV-1 Infection.

作者信息

Yu Jingyou, Liang Chen, Liu Shan-Lu

机构信息

From the Center for Retrovirus Research.

Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210.

出版信息

J Biol Chem. 2017 Mar 17;292(11):4674-4685. doi: 10.1074/jbc.M116.755819. Epub 2017 Jan 27.

Abstract

LY6E is a glycosylphosphatidylinositol-anchored, IFN-inducible protein that regulates T lymphocytes proliferation, differentiation, and development. Single-nucleotide polymorphism rs2572886 in the LY6 family protein locus has been shown to associate with accelerated progression to AIDS. In this study, we show that LY6E promotes HIV, type 1 (HIV-1) infection by enhancing viral entry and gene expression. Knockdown of LY6E in human peripheral blood mononuclear, SupT1, and THP-1 cells diminishes HIV-1 replication. Virion-cell and cell-cell fusion experiments revealed that LY6E promotes membrane fusion of the viral entry step. Interestingly, we find that LTR-driven HIV-1 gene expression is also enhanced by LY6E, suggesting additional roles of LY6E in HIV-1 replication. HIV-1 infection induces LY6E expression in human peripheral blood mononuclear cells, concomitant with increased production of type I IFN and some classical IFN-stimulated genes. Altogether, our results demonstrate that IFN-inducible LY6E promotes HIV-1 entry and replication and highlight a positive regulatory role of IFN-induced proteins in HIV-1 infection. Our work emphasizes the complexity of IFN-mediated signaling in HIV-host interaction and AIDS pathogenesis.

摘要

LY6E是一种糖基磷脂酰肌醇锚定的、干扰素诱导蛋白,可调节T淋巴细胞的增殖、分化和发育。LY6家族蛋白基因座中的单核苷酸多态性rs2572886已被证明与艾滋病进展加速有关。在本研究中,我们发现LY6E通过增强病毒进入和基因表达来促进1型人类免疫缺陷病毒(HIV-1)感染。在人外周血单个核细胞、SupT1细胞和THP-1细胞中敲低LY6E可减少HIV-1复制。病毒体-细胞和细胞-细胞融合实验表明,LY6E促进病毒进入步骤的膜融合。有趣的是,我们发现LY6E还能增强长末端重复序列(LTR)驱动的HIV-1基因表达,这表明LY6E在HIV-1复制中还有其他作用。HIV-1感染可诱导人外周血单个核细胞中LY6E表达,同时I型干扰素和一些经典干扰素刺激基因的产生增加。总之,我们的结果表明,干扰素诱导的LY6E促进HIV-1进入和复制,并突出了干扰素诱导蛋白在HIV-1感染中的正调控作用。我们的工作强调了干扰素介导的信号在HIV-宿主相互作用和艾滋病发病机制中的复杂性。

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