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In Vivo Labeling by CD73 Marks Multipotent Stromal Cells and Highlights Endothelial Heterogeneity in the Bone Marrow Niche.
Breitbach, Martin; Kimura, Kenichi; Luis, Tiago C; Fuegemann, Christopher J; Woll, Petter S; Hesse, Michael; Facchini, Raffaella; Rieck, Sarah; Jobin, Katarzyna; Reinhardt, Julia; Ohneda, Osamu; Wenzel, Daniela; Geisen, Caroline; Kurts, Christian; Kastenmüller, Wolfgang; Hölzel, Michael; Jacobsen, Sten E W; Fleischmann, Bernd K.
Afiliación
  • Breitbach M; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany. Electronic address: martin.breitbach@uni-bonn.de.
  • Kimura K; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany; Department of Cardiac Surgery, Medical Faculty, University of Bonn, 53105 Bonn, Germany; Department of Regenerative Medicine and Stem Cell Biology, University of Tsukuba, Tsukuba, Ibaraki 305-
  • Luis TC; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.
  • Fuegemann CJ; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany.
  • Woll PS; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK; Department of Medicine Huddinge, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Hesse M; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany; Department of Cardiac Surgery, Medical Faculty, University of Bonn, 53105 Bonn, Germany.
  • Facchini R; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.
  • Rieck S; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany.
  • Jobin K; Institute of Experimental Immunology, University of Bonn, 53105 Bonn, Germany.
  • Reinhardt J; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53105 Bonn, Germany.
  • Ohneda O; Department of Regenerative Medicine and Stem Cell Biology, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
  • Wenzel D; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany.
  • Geisen C; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany; Department of Cardiac Surgery, Medical Faculty, University of Bonn, 53105 Bonn, Germany.
  • Kurts C; Institute of Experimental Immunology, University of Bonn, 53105 Bonn, Germany.
  • Kastenmüller W; Institute of Experimental Immunology, University of Bonn, 53105 Bonn, Germany.
  • Hölzel M; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53105 Bonn, Germany.
  • Jacobsen SEW; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK; Department of Medicine Huddinge, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Cell and
  • Fleischmann BK; Institute of Physiology I, Life&Brain Center, Medical Faculty, University of Bonn, 53105 Bonn, Germany. Electronic address: bernd.fleischmann@uni-bonn.de.
Cell Stem Cell ; 22(2): 262-276.e7, 2018 02 01.
Article en En | MEDLINE | ID: mdl-29451855
Despite much work studying ex vivo multipotent stromal cells (MSCs), the identity and characteristics of MSCs in vivo are not well defined. Here, we generated a CD73-EGFP reporter mouse to address these questions and found EGFP+ MSCs in various organs. In vivo, EGFP+ mesenchymal cells were observed in fetal and adult bones at proliferative ossification sites, while in solid organs EGFP+ cells exhibited a perivascular distribution pattern. EGFP+ cells from the bone compartment could be clonally expanded ex vivo from single cells and displayed trilineage differentiation potential. Moreover, in the central bone marrow CD73-EGFP+ specifically labeled sinusoidal endothelial cells, thought to be a critical component of the hematopoietic stem cell niche. Purification and molecular characterization of this CD73-EGFP+ population revealed an endothelial subtype that also displays a mesenchymal signature, highlighting endothelial cell heterogeneity in the marrow. Thus, the CD73-EGFP mouse is a powerful tool for studying MSCs and sinusoidal endothelium.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Coloración y Etiquetado / Células de la Médula Ósea / 5'-Nucleotidasa / Células Madre Multipotentes / Células Endoteliales / Nicho de Células Madre Límite: Animals Idioma: En Revista: Cell Stem Cell Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Coloración y Etiquetado / Células de la Médula Ósea / 5'-Nucleotidasa / Células Madre Multipotentes / Células Endoteliales / Nicho de Células Madre Límite: Animals Idioma: En Revista: Cell Stem Cell Año: 2018 Tipo del documento: Article