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A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells

Clinical use of human pluripotent stem cells (hPSCs) is hampered by the technical limitations of their expansion. Here, we developed a chemically synthetic culture substrate for human pluripotent stem cell attachment and maintenance. The substrate comprises a hydrophobic polyvinyl butyral-based poly...

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Autores principales: Shimizu, Eiko, Iguchi, Hiroki, Le, Minh Nguyen Tuyet, Nakamura, Yuta, Kobayashi, Daigo, Arai, Yuhei, Takakura, Kenta, Benno, Seiko, Yoshida, Noriko, Tsukahara, Masayoshi, Haneda, Satoshi, Hasegawa, Kouichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847402/
https://www.ncbi.nlm.nih.gov/pubmed/35169157
http://dx.doi.org/10.1038/s41598-022-06356-8
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author Shimizu, Eiko
Iguchi, Hiroki
Le, Minh Nguyen Tuyet
Nakamura, Yuta
Kobayashi, Daigo
Arai, Yuhei
Takakura, Kenta
Benno, Seiko
Yoshida, Noriko
Tsukahara, Masayoshi
Haneda, Satoshi
Hasegawa, Kouichi
author_facet Shimizu, Eiko
Iguchi, Hiroki
Le, Minh Nguyen Tuyet
Nakamura, Yuta
Kobayashi, Daigo
Arai, Yuhei
Takakura, Kenta
Benno, Seiko
Yoshida, Noriko
Tsukahara, Masayoshi
Haneda, Satoshi
Hasegawa, Kouichi
author_sort Shimizu, Eiko
collection PubMed
description Clinical use of human pluripotent stem cells (hPSCs) is hampered by the technical limitations of their expansion. Here, we developed a chemically synthetic culture substrate for human pluripotent stem cell attachment and maintenance. The substrate comprises a hydrophobic polyvinyl butyral-based polymer (PVB) and a short peptide that enables easy and uniform coating of various types of cell culture ware. The coated ware exhibited thermotolerance, underwater stability and could be stored at room temperature. The substrate supported hPSC expansion in combination with most commercial culture media with an efficiency similar to that of commercial substrates. It supported not only the long-term expansion of examined iPS and ES cell lines with normal karyotypes during their undifferentiated state but also directed differentiation of three germ layers. This substrate resolves major concerns associated with currently used recombinant protein substrates and could be applied in large-scale automated manufacturing; it is suitable for affordable and stable production of clinical-grade hPSCs and hPSC-derived products.
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spelling pubmed-88474022022-02-17 A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells Shimizu, Eiko Iguchi, Hiroki Le, Minh Nguyen Tuyet Nakamura, Yuta Kobayashi, Daigo Arai, Yuhei Takakura, Kenta Benno, Seiko Yoshida, Noriko Tsukahara, Masayoshi Haneda, Satoshi Hasegawa, Kouichi Sci Rep Article Clinical use of human pluripotent stem cells (hPSCs) is hampered by the technical limitations of their expansion. Here, we developed a chemically synthetic culture substrate for human pluripotent stem cell attachment and maintenance. The substrate comprises a hydrophobic polyvinyl butyral-based polymer (PVB) and a short peptide that enables easy and uniform coating of various types of cell culture ware. The coated ware exhibited thermotolerance, underwater stability and could be stored at room temperature. The substrate supported hPSC expansion in combination with most commercial culture media with an efficiency similar to that of commercial substrates. It supported not only the long-term expansion of examined iPS and ES cell lines with normal karyotypes during their undifferentiated state but also directed differentiation of three germ layers. This substrate resolves major concerns associated with currently used recombinant protein substrates and could be applied in large-scale automated manufacturing; it is suitable for affordable and stable production of clinical-grade hPSCs and hPSC-derived products. Nature Publishing Group UK 2022-02-15 /pmc/articles/PMC8847402/ /pubmed/35169157 http://dx.doi.org/10.1038/s41598-022-06356-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shimizu, Eiko
Iguchi, Hiroki
Le, Minh Nguyen Tuyet
Nakamura, Yuta
Kobayashi, Daigo
Arai, Yuhei
Takakura, Kenta
Benno, Seiko
Yoshida, Noriko
Tsukahara, Masayoshi
Haneda, Satoshi
Hasegawa, Kouichi
A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title_full A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title_fullStr A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title_full_unstemmed A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title_short A chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
title_sort chemically-defined plastic scaffold for the xeno-free production of human pluripotent stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847402/
https://www.ncbi.nlm.nih.gov/pubmed/35169157
http://dx.doi.org/10.1038/s41598-022-06356-8
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