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干扰素诱导的 4 型异构体的过表达解析了包膜病毒的进入途径,并证明 HIV 通过融合进入细胞膜进入细胞。

Overexpression of the Interferon-Inducible Isoform 4 of Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane.

机构信息

Childhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, 171 76 Stockholm, Sweden.

Paediatric Oncology, Theme Women's and Children's Health, Karolinska University Hospital, 171 76 Stockholm, Sweden.

出版信息

Viruses. 2019 Jan 29;11(2):121. doi: 10.3390/v11020121.

Abstract

The HIV-1 entry-route is a matter of ongoing controversy, and there is evidence for fusion either at the cell surface or from within endosomes. A recent report demonstrated that isoform 4 of nuclear receptor coactivator 7 (NCOA7) interacts with endolysosomal vacuolar-type H⁺-ATPase (V-ATPase), increasing lytic activity and thereby severely affecting the entry of vesicular stomatitis virus glycoprotein (VSV-G)-mediated, but not HIV-Env-mediated, entry and infection. As basal expression of NCOA7 is low in the absence of type-1 interferons, its overexpression is a novel tool to study viral entry.

摘要

HIV-1 的进入途径是一个持续存在争议的问题,有证据表明融合要么发生在细胞表面,要么发生在内体中。最近的一份报告表明,核受体共激活因子 7(NCOA7)的同工型 4 与内体溶酶体液泡型 H⁺-ATP 酶(V-ATPase)相互作用,增加了裂解活性,从而严重影响了水疱性口炎病毒糖蛋白(VSV-G)介导的,但不是 HIV-Env 介导的进入和感染。由于 NCOA7 在缺乏 I 型干扰素的情况下表达水平较低,因此其过表达是研究病毒进入的新工具。

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