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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.show moreshow less

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Author details: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
Title of parent work (English):Stem Cell Reports
Publisher:Springer
Place of publishing:New York
Publication type:Article
Language:English
Date of first publication:2017/10/23
Publication year:2018
Release date:2021/10/29
Tag:aberrations; angiogenesis; cardiomyogenic differentiation; cord blood; efficient; expression; in vitro; progenitor cells; telomere dysfunction; virus infection
Volume:10
Issue:5
Number of pages:16
Funding institution:Universität Potsdam
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer review:Referiert
Publishing method:Open Access / Gold Open-Access
License (German):License LogoCC-BY-NC-ND - Namensnennung, nicht kommerziell, keine Bearbeitungen 4.0 International
External remark:Zweitveröffentlichung in der Schriftenreihe Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe ; 1182
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