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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
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.
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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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