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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8847402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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