The human bone marrow harbors a CD45- CD11B+ cell progenitor permitting rapid microglia-like cell derivative approaches.
Andreas BruzeliusIsabel HidalgoAntonio Boza-SerranoAnna-Giorgia HjelmérAmelie TisonTomas DeierborgJohan BengzonTania Ramos-MorenoPublished in: Stem cells translational medicine (2020)
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.
Keyphrases
- inflammatory response
- single cell
- neuropathic pain
- bone marrow
- lipopolysaccharide induced
- lps induced
- rna seq
- endothelial cells
- genome wide
- mesenchymal stem cells
- blood brain barrier
- cell therapy
- spinal cord injury
- spinal cord
- high throughput
- induced apoptosis
- poor prognosis
- gene expression
- cerebrospinal fluid
- immune response
- oxidative stress
- cell cycle arrest
- long non coding rna
- genome wide identification
- endoplasmic reticulum stress
- sensitive detection