Microglia and macrophages alterations in the CNS during acute SIV infection: A single-cell analysis in rhesus macaques.
Xiaoke XuMeng NiuBenjamin G LambertyKaty EmanuelShawn RamachandranAndrew J TreaseMehnaz TabassumJeffrey D LifsonHoward S FoxPublished in: PLoS pathogens (2024)
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.
Keyphrases
- inflammatory response
- human immunodeficiency virus
- single cell
- neuropathic pain
- antiretroviral therapy
- hiv infected
- liver failure
- hepatitis c virus
- immune response
- hiv positive
- rna seq
- blood brain barrier
- lipopolysaccharide induced
- drug induced
- hiv aids
- toll like receptor
- hiv testing
- respiratory failure
- genome wide
- oxidative stress
- dendritic cells
- lps induced
- high throughput
- cell proliferation
- sars cov
- risk assessment
- hepatitis b virus
- adipose tissue
- men who have sex with men
- cell death
- gene expression
- south africa
- acute myeloid leukemia
- intensive care unit
- white matter
- intellectual disability
- dna damage
- bone marrow
- endothelial cells
- current status
- transcription factor
- cerebrospinal fluid
- genome wide identification