A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres
Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) are an invaluable tool for both basic and translational cardiovascular research. The potential that these cells hold for therapy, disease modeling and drug discovery is hampered by several bottlenecks that currently limit b...
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doaj-a7803e37eb5249e49ce5d1ea8621a64b2020-11-25T01:02:14ZengElsevierStem Cell Research1873-50612018-10-01326572A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheresBenjamin Fischer0Anna Meier1Annika Dehne2Aseem Salhotra3Thao Anh Tran4Sascha Neumann5Katharina Schmidt6Ina Meiser7Julia C. Neubauer8Heiko Zimmermann9Luca Gentile10Fraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, Germany; Fraunhofer Project Centre for Stem Cell Process Engineering, Neunerplatz 2, Würzburg 97082, GermanyFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, Germany; Fraunhofer Project Centre for Stem Cell Process Engineering, Neunerplatz 2, Würzburg 97082, Germany; Saarland University, Gebäude A, Saarbrücken 66123, Germany; Universidad Católica del Norte, Larrondo 1281, Coquimbo 1780000, ChileFraunhofer Institute for Biomedical Engineering, Joseph-von-Fraunhofer-Weg 1, Sulzbach 66280, Germany; University of Applied Sciences Kaiserslautern, Campus Zweibrücken, Building G, Amerikastr. 1, Zweibrücken 66482, Germany; Hasselt University, Campus Diepenbeek, Diepenbeek 3590, Belgium; Corresponding author at: University of Applied Sciences Kaiserslautern, Campus Zweibrücken, Building G, Amerikastr. 1, 66482 Zweibrücken, Germany.Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) are an invaluable tool for both basic and translational cardiovascular research. The potential that these cells hold for therapy, disease modeling and drug discovery is hampered by several bottlenecks that currently limit both the yield and the efficiency of cardiac induction. Here, we present a complete workflow for the production of ready-to-use hiPSC-CMs in a dynamic suspension bioreactor. This includes the efficient and highly reproducible differentiation of hiPSCs into cardiospheres, which display enhanced physiological maturation compared to static 3D induction in hanging drops, and a novel papain-based dissociation method that offers higher yield and viability than the broadly used dissociation reagents TrypLE and Accutase. Molecular and functional analyses of the cardiomyocytes reseeded after dissociation confirmed both the identity and the functionality of the cells, which can be used in downstream applications, either as monolayers or spheroids. Keywords: hiPSCs, Cardiomyocytes, Cardiac induction, 3D bioreactor, Papain dissociationhttp://www.sciencedirect.com/science/article/pii/S1873506118302083 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Benjamin Fischer Anna Meier Annika Dehne Aseem Salhotra Thao Anh Tran Sascha Neumann Katharina Schmidt Ina Meiser Julia C. Neubauer Heiko Zimmermann Luca Gentile |
spellingShingle |
Benjamin Fischer Anna Meier Annika Dehne Aseem Salhotra Thao Anh Tran Sascha Neumann Katharina Schmidt Ina Meiser Julia C. Neubauer Heiko Zimmermann Luca Gentile A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres Stem Cell Research |
author_facet |
Benjamin Fischer Anna Meier Annika Dehne Aseem Salhotra Thao Anh Tran Sascha Neumann Katharina Schmidt Ina Meiser Julia C. Neubauer Heiko Zimmermann Luca Gentile |
author_sort |
Benjamin Fischer |
title |
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
title_short |
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
title_full |
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
title_fullStr |
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
title_full_unstemmed |
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
title_sort |
complete workflow for the differentiation and the dissociation of hipsc-derived cardiospheres |
publisher |
Elsevier |
series |
Stem Cell Research |
issn |
1873-5061 |
publishDate |
2018-10-01 |
description |
Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) are an invaluable tool for both basic and translational cardiovascular research. The potential that these cells hold for therapy, disease modeling and drug discovery is hampered by several bottlenecks that currently limit both the yield and the efficiency of cardiac induction. Here, we present a complete workflow for the production of ready-to-use hiPSC-CMs in a dynamic suspension bioreactor. This includes the efficient and highly reproducible differentiation of hiPSCs into cardiospheres, which display enhanced physiological maturation compared to static 3D induction in hanging drops, and a novel papain-based dissociation method that offers higher yield and viability than the broadly used dissociation reagents TrypLE and Accutase. Molecular and functional analyses of the cardiomyocytes reseeded after dissociation confirmed both the identity and the functionality of the cells, which can be used in downstream applications, either as monolayers or spheroids. Keywords: hiPSCs, Cardiomyocytes, Cardiac induction, 3D bioreactor, Papain dissociation |
url |
http://www.sciencedirect.com/science/article/pii/S1873506118302083 |
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