| Literature DB >> 30314756 |
Philip E Boulais1, Toshihide Mizoguchi2, Samuel Zimmerman3, Fumio Nakahara1, Judith Vivié4, Jessica C Mar5, Alexander van Oudenaarden4, Paul S Frenette6.
Abstract
The non-hematopoietic cell fraction of the bone marrow (BM) is classically identified as CD45- Ter119- CD31- (herein referred to as triple-negative cells or TNCs). Although TNCs are believed to contain heterogeneous stromal cell populations, they remain poorly defined. Here we showed that the vast majority of TNCs (∼85%) have a hematopoietic rather than mesenchymal origin. Single cell RNA-sequencing revealed erythroid and lymphoid progenitor signatures among CD51- TNCs. Ly6D+ CD44+ CD51- TNCs phenotypically and functionally resembled CD45+ pro-B lymphoid cells, whereas Ly6D- CD44+ CD51- TNCs were enriched in previously unappreciated stromal-dependent erythroid progenitors hierarchically situated between preCFU-E and proerythroblasts. Upon adoptive transfer, CD44+ CD51- TNCs contributed to repopulate the B-lymphoid and erythroid compartments. CD44+ CD51- TNCs also expanded during phenylhydrazine-induced acute hemolysis or in a model of sickle cell anemia. These findings thus uncover physiologically relevant new classes of stromal-associated functional CD45- hematopoietic progenitors.Entities:
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Year: 2018 PMID: 30314756 PMCID: PMC6377266 DOI: 10.1016/j.immuni.2018.08.019
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745