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. Bone marrow triple-negative CD45– Ter119– CD31– cells are thought to contain heterogeneous stromal cell populations. Boulais et al. show these cells are mostly hematopoietic in origin and contain previously unappreciated stromal-associated erythroid and B-lymphoid progenitor populations.
Original language | English |
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Pages (from-to) | 627-639.e6 |
Journal | Immunity |
Volume | 49 |
Issue number | 4 |
DOIs | |
State | Published - 16 Oct 2018 |
Externally published | Yes |