Abstract

Microglia, the immune sentinel of the central nervous system (CNS), are generated from yolk sac erythromyeloid progenitors that populate the developing CNS. Interestingly, a specific type of bone marrow-derived monocyte is able to express a yolk sac microglial signature and populate CNS in disease. Here we have examined human bone marrow (hBM) in an attempt to identify novel cell sources for generating microglia-like cells to use in cell-based therapies and in vitro modeling. We demonstrate that hBM stroma harbors a progenitor cell that we name stromal microglial progenitor (STR-MP). STR-MP single-cell gene analysis revealed the expression of the consensus genetic microglial signature and microglial-specific genes present in development and CNS pathologies. STR-MPs can be expanded and generate microglia-like cells in vitro, which we name stromal microglia (STR-M). STR-M cells show phagocytic ability, classically activate, and survive and phagocyte in human brain tissue. Thus, our results reveal that hBM harbors a source of microglia-like precursors that can be used in patient-centered fast derivative approaches.

Original languageEnglish
Pages (from-to)582-597
JournalStem cells translational medicine
Volume10
Issue number4
Early online date2020 Dec 9
DOIs
Publication statusPublished - 2021

Subject classification (UKÄ)

  • Neurosciences
  • Cell and Molecular Biology

Free keywords

  • bone marrow
  • common myeloid progenitor
  • human bone marrow
  • microglia
  • microglia-like cell in vitro model
  • microglial precursor
  • pluripotent stem cell
  • primitive myeloid progenitor

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