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A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells
In order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884228/ https://www.ncbi.nlm.nih.gov/pubmed/24399248 http://dx.doi.org/10.1038/srep03594 |
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author | Nakagawa, Masato Taniguchi, Yukimasa Senda, Sho Takizawa, Nanako Ichisaka, Tomoko Asano, Kanako Morizane, Asuka Doi, Daisuke Takahashi, Jun Nishizawa, Masatoshi Yoshida, Yoshinori Toyoda, Taro Osafune, Kenji Sekiguchi, Kiyotoshi Yamanaka, Shinya |
author_facet | Nakagawa, Masato Taniguchi, Yukimasa Senda, Sho Takizawa, Nanako Ichisaka, Tomoko Asano, Kanako Morizane, Asuka Doi, Daisuke Takahashi, Jun Nishizawa, Masatoshi Yoshida, Yoshinori Toyoda, Taro Osafune, Kenji Sekiguchi, Kiyotoshi Yamanaka, Shinya |
author_sort | Nakagawa, Masato |
collection | PubMed |
description | In order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve this goal, we developed a novel culture system. We found that recombinant laminin-511 E8 fragments are useful matrices for maintaining hESCs and hiPSCs when used in combination with a completely xeno-free (Xf) medium, StemFit™. Using this system, hESCs and hiPSCs can be easily and stably passaged by dissociating the cells into single cells for long periods, without any karyotype abnormalities. Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human primary fibroblasts and blood cells, and they possessed differentiation abilities. These results indicate that hiPSCs can be generated and maintained under this novel Ff and Xf culture system. |
format | Online Article Text |
id | pubmed-3884228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38842282014-01-08 A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells Nakagawa, Masato Taniguchi, Yukimasa Senda, Sho Takizawa, Nanako Ichisaka, Tomoko Asano, Kanako Morizane, Asuka Doi, Daisuke Takahashi, Jun Nishizawa, Masatoshi Yoshida, Yoshinori Toyoda, Taro Osafune, Kenji Sekiguchi, Kiyotoshi Yamanaka, Shinya Sci Rep Article In order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve this goal, we developed a novel culture system. We found that recombinant laminin-511 E8 fragments are useful matrices for maintaining hESCs and hiPSCs when used in combination with a completely xeno-free (Xf) medium, StemFit™. Using this system, hESCs and hiPSCs can be easily and stably passaged by dissociating the cells into single cells for long periods, without any karyotype abnormalities. Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human primary fibroblasts and blood cells, and they possessed differentiation abilities. These results indicate that hiPSCs can be generated and maintained under this novel Ff and Xf culture system. Nature Publishing Group 2014-01-08 /pmc/articles/PMC3884228/ /pubmed/24399248 http://dx.doi.org/10.1038/srep03594 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Nakagawa, Masato Taniguchi, Yukimasa Senda, Sho Takizawa, Nanako Ichisaka, Tomoko Asano, Kanako Morizane, Asuka Doi, Daisuke Takahashi, Jun Nishizawa, Masatoshi Yoshida, Yoshinori Toyoda, Taro Osafune, Kenji Sekiguchi, Kiyotoshi Yamanaka, Shinya A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title | A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title_full | A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title_fullStr | A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title_full_unstemmed | A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title_short | A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
title_sort | novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884228/ https://www.ncbi.nlm.nih.gov/pubmed/24399248 http://dx.doi.org/10.1038/srep03594 |
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