AI Article Synopsis

  • * The exact cellular types responsible for this immune activation and neuronal damage are largely unknown, largely due to the difficulty of accessing CNS cells in living humans.
  • * A study using single-cell RNA sequencing revealed a rare myeloid cell subset in cerebrospinal fluid that shares a gene expression profile with microglia linked to neurodegenerative diseases, showing the potential of this technique to uncover important immune cell dynamics in CNS disorders.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237230PMC
http://dx.doi.org/10.1172/jci.insight.121718DOI Listing

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