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Differentiation of Human Pluripotent Stem Cells into Functional Endothelial Cells in Scalable Suspension Culture

  • Endothelial cells (ECs) are involved in a variety of cellular responses. As multifunctional components of vascular structures, endothelial (progenitor) cells have been utilized in cellular therapies and are required as an important cellular component of engineered tissue constructs and in vitro disease models. Although primary ECs from different sources are readily isolated and expanded, cell quantity and quality in terms of functionality and karyotype stability is limited. ECs derived from human induced pluripotent stem cells (hiPSCs) represent an alternative and potentially superior cell source, but traditional culture approaches and 2D differentiation protocols hardly allow for production of large cell numbers. Aiming at the production of ECs, we have developed a robust approach for efficient endothelial differentiation of hiPSCs in scalable suspension culture. The established protocol results in relevant numbers of ECs for regenerative approaches and industrial applications that show in vitro proliferation capacity and a highEndothelial cells (ECs) are involved in a variety of cellular responses. As multifunctional components of vascular structures, endothelial (progenitor) cells have been utilized in cellular therapies and are required as an important cellular component of engineered tissue constructs and in vitro disease models. Although primary ECs from different sources are readily isolated and expanded, cell quantity and quality in terms of functionality and karyotype stability is limited. ECs derived from human induced pluripotent stem cells (hiPSCs) represent an alternative and potentially superior cell source, but traditional culture approaches and 2D differentiation protocols hardly allow for production of large cell numbers. Aiming at the production of ECs, we have developed a robust approach for efficient endothelial differentiation of hiPSCs in scalable suspension culture. The established protocol results in relevant numbers of ECs for regenerative approaches and industrial applications that show in vitro proliferation capacity and a high degree of chromosomal stability.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Ruth OlmerORCiDGND, Lena EngelsGND, Abdulai UsmanORCiD, Sandra Menke, Muhammad Nasir Hayat MalikORCiDGND, Frank PesslerORCiDGND, Gudrun GoehringORCiDGND, Dorothee BornhorstORCiDGND, Svenja BoltenGND, Salim Abdelilah-SeyfriedORCiDGND, Thomas ScheperORCiDGND, Henning KempfORCiDGND, Robert ZweigerdtORCiDGND, Ulrich MartinORCiD
DOI:https://doi.org/10.1016/j.stemcr.2018.03.017
ISSN:2213-6711
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/29681541
Titel des übergeordneten Werks (Englisch):Stem Cell Reports
Verlag:Springer
Verlagsort:New York
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:23.10.2017
Erscheinungsjahr:2018
Datum der Freischaltung:29.10.2021
Freies Schlagwort / Tag:aberrations; angiogenesis; cardiomyogenic differentiation; cord blood; efficient; expression; in vitro; progenitor cells; telomere dysfunction; virus infection
Band:10
Ausgabe:5
Seitenanzahl:16
Fördernde Institution:Universität Potsdam
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
Publikationsweg:Open Access / Gold Open-Access
Lizenz (Deutsch):License LogoCC-BY-NC-ND - Namensnennung, nicht kommerziell, keine Bearbeitungen 4.0 International
Externe Anmerkung:Zweitveröffentlichung in der Schriftenreihe Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe ; 1182
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