人类免疫缺陷病毒(HIV-1)通过无细胞感染和细胞相关感染攻击星形胶质细胞

IF 2.5 4区 医学 Q3 NEUROSCIENCES
Roberta S Dos Reis, Stephen Susa, Marc C E Wagner, Velpandi Ayyavoo
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引用次数: 0

摘要

背景:人类免疫缺陷病毒(HIV-1)感染星形胶质细胞仍是一个争论不休的话题,数据相互矛盾,但在体内已观察到星形胶质细胞含有病毒 DNA 的实例。在这项研究中,我们旨在利用原代人类星形胶质细胞阐明星形胶质细胞可能的感染途径及其产生感染性颗粒的能力:我们使用无细胞 HIV-1 病毒直接感染了从神经祖细胞(NPC)或诱导多能干细胞(iPSC)提取的原代星形胶质细胞,这些细胞同时表达 C-X-C 趋化因子受体 4 型(CXCR4)和 C-C 趋化因子受体 5 型(CCR5)核心受体:结果:无细胞病毒的低水平感染性主要归因于进入过程中的缺陷。使用伪型病毒绕过艾滋病毒特异性受体介导的进入过程,可产生感染并释放感染性颗粒:这些研究结果表明,星形胶质细胞可能是艾滋病相关神经认知障碍(HAND)的潜在神经毒性来源之一,并有可能成为中枢神经系统(CNS)中的艾滋病病毒库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Immunodeficiency Virus (HIV-1) Targets Astrocytes via Cell-Free and Cell-Associated Infection.

Background: Infection of astrocytes by Human Immunodeficiency Virus (HIV-1) remains a topic of debate, with conflicting data, yet instances of astrocytes containing viral DNA have been observed in vivo. In this study, we aimed to elucidate potential routes through which astrocytes could be infected and their ability to produce infectious particles using primary human astrocytes.

Methods: We infected primary astrocytes derived from either neuroprogenitor cells (NPCs) or induced pluripotent stem cells (iPSCs) that express both C-X-C chemokine receptor type 4 (CXCR4) and the C-C chemokine receptor type 5 (CCR5) coreceptors, using either cell-free HIV-1 virus directly or cell-associated virus indirectly through infected macrophages and microglia.

Results: Low-level infectivity by cell-free viruses was primarily attributed to a defect in the entry process. Bypassing HIV-specific receptor-mediated entry using pseudotyped viruses resulted in productive infection and the release of infectious particles.

Conclusions: These findings suggest that astrocytes may be one of the potential sources of neurotoxicity in HIV-associated neurocognitive disorders (HAND) and could possibly act as reservoirs for HIV in the central nervous system (CNS).

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来源期刊
CiteScore
2.80
自引率
5.60%
发文量
173
审稿时长
2 months
期刊介绍: JIN is an international peer-reviewed, open access journal. JIN publishes leading-edge research at the interface of theoretical and experimental neuroscience, focusing across hierarchical levels of brain organization to better understand how diverse functions are integrated. We encourage submissions from scientists of all specialties that relate to brain functioning.
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