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Single-cell RNA sequencing reveals microglia-like cells in cerebrospinal fluid during virologically suppressed HIV
Shelli F. Farhadian, … , David A. Hafler, Serena S. Spudich
Shelli F. Farhadian, … , David A. Hafler, Serena S. Spudich
Published September 20, 2018
Citation Information: JCI Insight. 2018;3(18):e121718. https://doi.org/10.1172/jci.insight.121718.
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Research Article AIDS/HIV Inflammation

Single-cell RNA sequencing reveals microglia-like cells in cerebrospinal fluid during virologically suppressed HIV

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Abstract

Central nervous system (CNS) immune activation is an important driver of neuronal injury during several neurodegenerative and neuroinflammatory diseases. During HIV infection, CNS immune activation is associated with high rates of neurocognitive impairment, even during sustained long-term suppressive antiretroviral therapy (ART). However, the cellular subsets that drive immune activation and neuronal damage in the CNS during HIV infection and other neurological conditions remain unknown, in part because CNS cells are difficult to access in living humans. Using single-cell RNA sequencing (scRNA-seq) on cerebrospinal fluid (CSF) and blood from adults with and without HIV, we identified a rare (<5% of cells) subset of myeloid cells that are found only in CSF and that present a gene expression signature that overlaps significantly with neurodegenerative disease–associated microglia. This highlights the power of scRNA-seq of CSF to identify rare CNS immune cell subsets that may perpetuate neuronal injury during HIV infection and other conditions.

Authors

Shelli F. Farhadian, Sameet S. Mehta, Chrysoula Zografou, Kevin Robertson, Richard W. Price, Jenna Pappalardo, Jennifer Chiarella, David A. Hafler, Serena S. Spudich

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Figure 2

Single-cell RNA sequencing reveals a disease-associated microglia-like cellular subset in cerebrospinal fluid.

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Single-cell RNA sequencing reveals a disease-associated microglia-like c...
(A) Heatmap showing the top 15 genes whose expression levels are highest and most differentiating in each of the 5 myeloid subsets. (B) Venn diagram shows genes that were found in Myeloid-2 (blue) and across 2 independent transcriptomic studies of neurodegenerative disease–associated microglial cells derived from mouse brain (green [ref. 16] and orange [ref. 27]), with P < 10–13 and P < 10–4 for the probability of finding overlapping genes when comparing the Myeloid-2 subset to refs. 26 and 27, respectively). (C) Examination of an independent CSF sample from an HIV+ participant (HIV3) reveals a group of cells with high expression of the genes that characterize the CSF microglia-like myeloid subset (Myeloid-2). (D) Box plots showing the percentage of Myeloid-2 transcripts per cell in HIV+ CSF (n = 5,919 pooled cells), uninfected CSF (n = 1,770 pooled), and blood (n = 5,581 pooled cells), with P values comparing the distribution of Myeloid-2 transcripts between samples (Wilcoxon’s rank-sum test). Shown are the median (black line) and 25th and 75th percentiles (box outlines).

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