Your browser doesn't support javascript.
loading
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.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-31279774
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.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Estrés Fisiológico / Células de la Médula Ósea / Células del Estroma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cell Stem Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Estrés Fisiológico / Células de la Médula Ósea / Células del Estroma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cell Stem Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos