急性 SIV 感染期间中枢神经系统小胶质细胞和巨噬细胞的变化:猕猴的单细胞分析。

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2024-09-16 eCollection Date: 2024-09-01 DOI:10.1371/journal.ppat.1012168
Xiaoke Xu, Meng Niu, Benjamin G Lamberty, Katy Emanuel, Shawn Ramachandran, Andrew J Trease, Mehnaz Tabassum, Jeffrey D Lifson, Howard S Fox
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引用次数: 0

摘要

人类免疫缺陷病毒(HIV)因其对免疫系统的深远影响而广为人知。尽管 HIV 主要影响外周 CD4 T 细胞,但它对中枢神经系统(CNS)的影响也不容忽视。在非人灵长类动物的大脑中,小胶质细胞和中枢神经系统相关巨噬细胞(CAMs)是 HIV 和猿猴免疫缺陷病毒(SIV)的主要目标。这种感染可导致神经系统效应并建立病毒库。鉴于我们对这些细胞如何在体内对急性中枢神经系统感染做出反应的认识存在空白,我们对三只猕猴在感染 SIV 12 天后的脑髓细胞以及三只未感染对照组的脑髓细胞进行了单细胞 RNA 测序(scRNA-seq)。我们的分析发现了六个不同的小胶质细胞群,包括表达高水平炎症和疾病相关分子的稳态小胶质细胞、预激活小胶质细胞和激活小胶质细胞。对急性 SIV 感染做出反应时,静态和预激活的小胶质细胞数量减少,而激活和疾病相关的小胶质细胞数量增加。所有小胶质细胞集群都表现出 MHC I 类分子和干扰素相关基因的上调,表明它们在急性期抵御 SIV 的关键作用。所有小胶质细胞集群还上调了与细胞衰老相关的基因。此外,我们还发现了两种不同的 CAM 群体:CD14lowCD16hi 和 CD14hiCD16low CAMs。有趣的是,在急性 SIV 感染期间,主要的 CAM 群体转变为具有炎症表型的 CAM 群体。一个小胶质细胞集群和一个巨噬细胞集群中的特定上调基因与神经退行性病变途径有关,这表明它们与神经认知障碍有潜在联系。这项研究揭示了病毒感染、先天性免疫反应和中枢神经系统之间错综复杂的相互作用,为今后的研究提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microglia and macrophages alterations in the CNS during acute SIV infection: A single-cell analysis in rhesus macaques.

Human Immunodeficiency Virus (HIV) is widely acknowledged for its profound impact on the immune system. Although HIV primarily affects peripheral CD4 T cells, its influence on the central nervous system (CNS) cannot be overlooked. Within the brain, microglia and CNS-associated macrophages (CAMs) serve as the primary targets for HIV and the simian immunodeficiency virus (SIV) in nonhuman primates. This infection can lead to neurological effects and establish a viral reservoir. Given the gaps in our understanding of how these cells respond in vivo to acute CNS infection, we conducted single-cell RNA sequencing (scRNA-seq) on myeloid cells from the brains of three rhesus macaques 12 days after SIV infection, along with three uninfected controls. Our analysis revealed six distinct microglial clusters including homeostatic microglia, preactivated microglia, and activated microglia expressing high levels of inflammatory and disease-related molecules. In response to acute SIV infection, the homeostatic and preactivated microglia population decreased, while the activated and disease-related microglia increased. All microglial clusters exhibited upregulation of MHC class I molecules and interferon-related genes, indicating their crucial roles in defending against SIV during the acute phase. All microglia clusters also upregulated genes linked to cellular senescence. Additionally, we identified two distinct CAM populations: CD14lowCD16hi and CD14hiCD16low CAMs. Interestingly, during acute SIV infection, the dominant CAM population changed to one with an inflammatory phenotype. Specific upregulated genes within one microglia and one macrophage cluster were associated with neurodegenerative pathways, suggesting potential links to neurocognitive disorders. This research sheds light on the intricate interactions between viral infection, innate immune responses, and the CNS, providing valuable insights for future investigations.

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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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