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Identification of factors promoting ex vivo maintenance of mouse hematopoietic stem cells by long-term single-cell quantification.
Kokkaliaris, Konstantinos D; Drew, Erin; Endele, Max; Loeffler, Dirk; Hoppe, Philipp S; Hilsenbeck, Oliver; Schauberger, Bernhard; Hinzen, Christoph; Skylaki, Stavroula; Theodorou, Marina; Kieslinger, Matthias; Lemischka, Ihor; Moore, Kateri; Schroeder, Timm.
Afiliação
  • Kokkaliaris KD; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Drew E; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany;
  • Endele M; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Loeffler D; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Hoppe PS; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Hilsenbeck O; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Schauberger B; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany;
  • Hinzen C; Institute of Clinical Molecular Biology and Tumor Genetics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Munich, Germany;
  • Skylaki S; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
  • Theodorou M; Institute for Developmental Genetics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; and.
  • Kieslinger M; Institute of Clinical Molecular Biology and Tumor Genetics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Munich, Germany;
  • Lemischka I; Department of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Moore K; Department of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Schroeder T; Research Unit Stem Cell Dynamics, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), Neuherberg, Germany; Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zurich, Basel, Switzerland;
Blood ; 128(9): 1181-92, 2016 09 01.
Article em En | MEDLINE | ID: mdl-27365423
The maintenance of hematopoietic stem cells (HSCs) during ex vivo culture is an important prerequisite for their therapeutic manipulation. However, despite intense research, culture conditions for robust maintenance of HSCs are still missing. Cultured HSCs are quickly lost, preventing their improved analysis and manipulation. Identification of novel factors supporting HSC ex vivo maintenance is therefore necessary. Coculture with the AFT024 stroma cell line is capable of maintaining HSCs ex vivo long-term, but the responsible molecular players remain unknown. Here, we use continuous long-term single-cell observation to identify the HSC behavioral signature under supportive or nonsupportive stroma cocultures. We report early HSC survival as a major characteristic of HSC-maintaining conditions. Behavioral screening after manipulation of candidate molecules revealed that the extracellular matrix protein dermatopontin (Dpt) is involved in HSC maintenance. DPT knockdown in supportive stroma impaired HSC survival, whereas ectopic expression of the Dpt gene or protein in nonsupportive conditions restored HSC survival. Supplementing defined stroma- and serum-free culture conditions with recombinant DPT protein improved HSC clonogenicity. These findings illustrate a previously uncharacterized role of Dpt in maintaining HSCs ex vivo.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteoglicanas de Sulfatos de Condroitina / Células-Tronco Hematopoéticas / Proteínas da Matriz Extracelular Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteoglicanas de Sulfatos de Condroitina / Células-Tronco Hematopoéticas / Proteínas da Matriz Extracelular Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article