| Literature DB >> 33295698 |
Andreas Bruzelius1,2, Isabel Hidalgo1,3, Antonio Boza-Serrano4,5, Anna-Giorgia Hjelmér1, Amelie Tison1, Tomas Deierborg5, Johan Bengzon1, Tania Ramos-Moreno1,5.
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.Entities:
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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Year: 2020 PMID: 33295698 PMCID: PMC7980218 DOI: 10.1002/sctm.20-0127
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 6.940