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P选择素糖蛋白配体-1(PSGL-1)通过限制肌动蛋白动力学和隔离HIV包膜蛋白来抑制HIV-1感染。

PSGL-1 inhibits HIV-1 infection by restricting actin dynamics and sequestering HIV envelope proteins.

作者信息

Liu Ying, Song Yutong, Zhang Siyu, Diao Min, Huang Shanjin, Li Sai, Tan Xu

机构信息

Beijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center for Biological Structure, MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, School of Pharmaceutical Sciences, Center for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, 100084 China.

Beijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center for Biological Structure, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, 100084 China.

出版信息

Cell Discov. 2020 Aug 4;6:53. doi: 10.1038/s41421-020-0184-9. eCollection 2020.

Abstract

PSGL-1 has recently been identified as an HIV restriction factor that inhibits HIV DNA synthesis and more potently, virion infectivity. But the underlying mechanisms of these inhibitions are unknown. Here we show that PSGL-1 directly binds to cellular actin filaments (F-actin) to restrict actin dynamics, which leads to inhibition of HIV DNA synthesis. PSGL-1 is incorporated into nascent virions and restricts actin dynamics in the virions, which partially accounts for the inhibition of virion infectivity. More potently, PSGL-1 inhibits incorporation of Env proteins into nascent virions, causing a loss of envelope spikes on the virions as shown by Cryo-electron microscopy and super-resolution imaging. This loss is associated with a profound defect in viral entry. Mechanistically, PSGL-1 binds gp41 and sequesters gp41 at the plasma membrane, explaining the inhibition of Env incorporation in nascent virions. PSGL-1's dual anti-HIV mechanisms represent novel strategies of human cells to defend against HIV infection.

摘要

PSGL-1最近被鉴定为一种HIV限制因子,它能抑制HIV DNA合成,更有效地抑制病毒体感染性。但这些抑制作用的潜在机制尚不清楚。在这里,我们表明PSGL-1直接与细胞肌动蛋白丝(F-肌动蛋白)结合,以限制肌动蛋白动力学,从而导致HIV DNA合成受到抑制。PSGL-1被整合到新生病毒体中,并限制病毒体中的肌动蛋白动力学,这部分解释了病毒体感染性的抑制。更重要的是,PSGL-1抑制Env蛋白整合到新生病毒体中,如冷冻电子显微镜和超分辨率成像所示,导致病毒体上包膜刺突的丧失。这种丧失与病毒进入的严重缺陷有关。从机制上讲,PSGL-1结合gp41并将gp41隔离在质膜上,这解释了新生病毒体中Env整合的抑制。PSGL-1的双重抗HIV机制代表了人类细胞抵御HIV感染的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c282/7400672/ff70480f918d/41421_2020_184_Fig1_HTML.jpg

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