Department of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Department of Pathology, Microbiology, and Immunology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
PLoS Pathog. 2024 Sep 16;20(9):e1012168. doi: 10.1371/journal.ppat.1012168. eCollection 2024 Sep.
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.
人类免疫缺陷病毒 (HIV) 对免疫系统的影响是众所周知的。尽管 HIV 主要影响外周血 CD4 T 细胞,但它对中枢神经系统 (CNS) 的影响不容忽视。在大脑中,小胶质细胞和中枢神经系统相关巨噬细胞 (CAM) 是 HIV 和非人类灵长类动物中的猴免疫缺陷病毒 (SIV) 的主要靶标。这种感染可导致神经效应并建立病毒储存库。鉴于我们对这些细胞在体内如何对急性中枢神经系统感染做出反应的理解存在差距,我们对 SIV 感染后 12 天的三只恒河猴大脑中的髓样细胞进行了单细胞 RNA 测序 (scRNA-seq),并与三个未感染对照进行了比较。我们的分析揭示了六个不同的小胶质细胞簇,包括稳态小胶质细胞、预激活小胶质细胞和表达高水平炎症和疾病相关分子的激活小胶质细胞。在急性 SIV 感染时,稳态和预激活小胶质细胞群减少,而激活和疾病相关小胶质细胞增加。所有小胶质细胞簇均上调 MHC Ⅰ类分子和干扰素相关基因,表明它们在急性期中对抗 SIV 具有至关重要的作用。所有小胶质细胞簇也上调了与细胞衰老相关的基因。此外,我们还鉴定了两种不同的 CAM 群体:CD14lowCD16hi 和 CD14hiCD16lowCAM。有趣的是,在急性 SIV 感染期间,主导的 CAM 群体转变为具有炎症表型的群体。一个小胶质细胞和一个巨噬细胞簇中特定上调的基因与神经退行性途径相关,表明与神经认知障碍存在潜在联系。这项研究揭示了病毒感染、先天免疫反应和中枢神经系统之间的复杂相互作用,为未来的研究提供了有价值的见解。