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Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture

Insulin-producing cells (IPCs) derived from human pluripotent stem cells (hPSCs) may be useful in cell therapy and drug discovery for diabetes. Here, we examined various growth factors and small molecules including those previously reported to develop a robust differentiation method for induction of...

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Detalles Bibliográficos
Autores principales: Takeuchi, Hiroki, Nakatsuji, Norio, Suemori, Hirofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967149/
https://www.ncbi.nlm.nih.gov/pubmed/24671046
http://dx.doi.org/10.1038/srep04488
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author Takeuchi, Hiroki
Nakatsuji, Norio
Suemori, Hirofumi
author_facet Takeuchi, Hiroki
Nakatsuji, Norio
Suemori, Hirofumi
author_sort Takeuchi, Hiroki
collection PubMed
description Insulin-producing cells (IPCs) derived from human pluripotent stem cells (hPSCs) may be useful in cell therapy and drug discovery for diabetes. Here, we examined various growth factors and small molecules including those previously reported to develop a robust differentiation method for induction of mature IPCs from hPSCs. We established a protocol that induced PDX1-positive pancreatic progenitor cells at high efficiency, and further induced mature IPCs by treatment with forskolin, dexamethasone, Alk5 inhibitor II and nicotinamide in 3D culture. The cells that differentiated into INSULIN-positive and C-PEPTIDE-positive cells secreted insulin in response to glucose stimulation, indicating a functional IPC phenotype. We also found that this method was applicable to different types of hPSCs.
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spelling pubmed-39671492014-03-27 Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture Takeuchi, Hiroki Nakatsuji, Norio Suemori, Hirofumi Sci Rep Article Insulin-producing cells (IPCs) derived from human pluripotent stem cells (hPSCs) may be useful in cell therapy and drug discovery for diabetes. Here, we examined various growth factors and small molecules including those previously reported to develop a robust differentiation method for induction of mature IPCs from hPSCs. We established a protocol that induced PDX1-positive pancreatic progenitor cells at high efficiency, and further induced mature IPCs by treatment with forskolin, dexamethasone, Alk5 inhibitor II and nicotinamide in 3D culture. The cells that differentiated into INSULIN-positive and C-PEPTIDE-positive cells secreted insulin in response to glucose stimulation, indicating a functional IPC phenotype. We also found that this method was applicable to different types of hPSCs. Nature Publishing Group 2014-03-27 /pmc/articles/PMC3967149/ /pubmed/24671046 http://dx.doi.org/10.1038/srep04488 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Takeuchi, Hiroki
Nakatsuji, Norio
Suemori, Hirofumi
Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title_full Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title_fullStr Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title_full_unstemmed Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title_short Endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3D culture
title_sort endodermal differentiation of human pluripotent stem cells to insulin-producing cells in 3d culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967149/
https://www.ncbi.nlm.nih.gov/pubmed/24671046
http://dx.doi.org/10.1038/srep04488
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