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 language | English |
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Pages (from-to) | 582-597 |
Journal | Stem cells translational medicine |
Volume | 10 |
Issue number | 4 |
Early online date | 2020 Dec 9 |
DOIs | |
Publication status | Published - 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