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Stress-Induced Changes in Bone Marrow Stromal Cell Populations Revealed through Single-Cell Protein Expression Mapping.
Severe, Nicolas; Karabacak, Nezihi Murat; Gustafsson, Karin; Baryawno, Ninib; Courties, Gabriel; Kfoury, Youmna; Kokkaliaris, Konstantinos D; Rhee, Catherine; Lee, Dongjun; Scadden, Elizabeth W; Garcia-Robledo, Juan Esteban; Brouse, Thomas; Nahrendorf, Matthias; Toner, Mehmet; Scadden, David T.
Afiliação
  • Severe N; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Karabacak NM; BioMEMS Resource Center, Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA; Shriners Hospital for Children, Boston, MA 02114, USA.
  • Gustafsson K; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Baryawno N; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Courties G; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Kfoury Y; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Kokkaliaris KD; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Rhee C; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Lee D; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Scadden EW; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Garcia-Robledo JE; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Brouse T; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Nahrendorf M; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Toner M; BioMEMS Resource Center, Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA; Shriners Hospital for Children, Boston, MA 02114, USA.
  • Scadden DT; Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA; Harvard Stem Cell Institute, 7 Divinity Ave., Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA. Electronic address: davi
Cell Stem Cell ; 25(4): 570-583.e7, 2019 Oct 03.
Article em En | MEDLINE | ID: mdl-31279774
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Fisiológico / Células da Medula Óssea / Células Estromais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cell Stem Cell Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Fisiológico / Células da Medula Óssea / Células Estromais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cell Stem Cell Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos