| Literature DB >> 31279774 |
Nicolas Severe1, Nezihi Murat Karabacak2, Karin Gustafsson1, Ninib Baryawno1, Gabriel Courties3, Youmna Kfoury1, Konstantinos D Kokkaliaris1, Catherine Rhee1, Dongjun Lee1, Elizabeth W Scadden1, Juan Esteban Garcia-Robledo1, Thomas Brouse1, Matthias Nahrendorf3, Mehmet Toner2, David T Scadden4.
Abstract
Stromal cell populations that maintain hematopoietic stem and progenitor cells (HSPCs) are generally characterized in steady-state conditions. Here, we report a comprehensive atlas of bone marrow stromal cell subpopulations under homeostatic and stress conditions using mass cytometry (CyTOF)-based single-cell protein analysis. We identified 28 subsets of non-hematopoietic cells during homeostasis, 14 of which expressed hematopoietic regulatory factors. Irradiation-based conditioning for HSPC transplantation led to the loss of most of these populations, including the LeptinR+ and Nestin+ subsets. In contrast, a subset expressing Ecto-5'-nucleotidase (CD73) was retained and a specific CD73+NGFRhigh population expresses high levels of cytokines during homeostasis and stress. Genetic ablation of CD73 compromised HSPC transplantation in an acute setting without long-term changes in bone marrow HSPCs. Thus, this protein-based expression mapping reveals distinct sets of stromal cells in the bone marrow and how they change in clinically relevant stress settings to contribute to early stages of hematopoietic regeneration.Entities:
Keywords: acute blood regeneration; bone marrow stromal cells; bone marrow transplantation; ecto-5′-nucleotidase; hematopoietic stress; mass cytometry; stem cell niche; stromal heterogeneity
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Year: 2019 PMID: 31279774 PMCID: PMC6778015 DOI: 10.1016/j.stem.2019.06.003
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633