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An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations

Clinical application of human induced pluripotent stem cells (hiPSCs) has been hampered by the lack of a practical, scalable culture system. Stacked culture plates (SCPs) have recently attracted attention. However, final cell yields depend on the efficiency of cell detachment, and inefficient cell r...

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Autores principales: Terao, Yusuke, Kurashina, Yuta, Tohyama, Shugo, Fukuma, Yuki, Fukuda, Keiichi, Fujita, Jun, Takemura, Kenjiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821886/
https://www.ncbi.nlm.nih.gov/pubmed/31666563
http://dx.doi.org/10.1038/s41598-019-51944-w
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author Terao, Yusuke
Kurashina, Yuta
Tohyama, Shugo
Fukuma, Yuki
Fukuda, Keiichi
Fujita, Jun
Takemura, Kenjiro
author_facet Terao, Yusuke
Kurashina, Yuta
Tohyama, Shugo
Fukuma, Yuki
Fukuda, Keiichi
Fujita, Jun
Takemura, Kenjiro
author_sort Terao, Yusuke
collection PubMed
description Clinical application of human induced pluripotent stem cells (hiPSCs) has been hampered by the lack of a practical, scalable culture system. Stacked culture plates (SCPs) have recently attracted attention. However, final cell yields depend on the efficiency of cell detachment, and inefficient cell recovery from SCPs presents a major challenge to their use. We have developed an effective detachment method using resonance vibrations (RVs) of substrates with sweeping driving frequency. By exciting RVs that have 1–3 antinodes with ultra-low-density enzyme spread on each substrate of SCPs, 87.8% of hiPSCs were successfully detached from a 5-layer SCP compared to 30.8% detached by the conventional enzymatic method. hiPSC viability was similar after either method. Moreover, hiPSCs detached by the RV method maintained their undifferentiated state. Additionally, hiPSCs after long-term culture (10 passages) kept excellent detachment efficiency, had the normal karyotypes, and maintained the undifferentiated state and pluripotency. These results indicated that the RV method has definite advantages over the conventional enzymatic method in the scalable culture of hiPSCs using SCPs.
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spelling pubmed-68218862019-11-05 An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations Terao, Yusuke Kurashina, Yuta Tohyama, Shugo Fukuma, Yuki Fukuda, Keiichi Fujita, Jun Takemura, Kenjiro Sci Rep Article Clinical application of human induced pluripotent stem cells (hiPSCs) has been hampered by the lack of a practical, scalable culture system. Stacked culture plates (SCPs) have recently attracted attention. However, final cell yields depend on the efficiency of cell detachment, and inefficient cell recovery from SCPs presents a major challenge to their use. We have developed an effective detachment method using resonance vibrations (RVs) of substrates with sweeping driving frequency. By exciting RVs that have 1–3 antinodes with ultra-low-density enzyme spread on each substrate of SCPs, 87.8% of hiPSCs were successfully detached from a 5-layer SCP compared to 30.8% detached by the conventional enzymatic method. hiPSC viability was similar after either method. Moreover, hiPSCs detached by the RV method maintained their undifferentiated state. Additionally, hiPSCs after long-term culture (10 passages) kept excellent detachment efficiency, had the normal karyotypes, and maintained the undifferentiated state and pluripotency. These results indicated that the RV method has definite advantages over the conventional enzymatic method in the scalable culture of hiPSCs using SCPs. Nature Publishing Group UK 2019-10-30 /pmc/articles/PMC6821886/ /pubmed/31666563 http://dx.doi.org/10.1038/s41598-019-51944-w Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Terao, Yusuke
Kurashina, Yuta
Tohyama, Shugo
Fukuma, Yuki
Fukuda, Keiichi
Fujita, Jun
Takemura, Kenjiro
An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title_full An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title_fullStr An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title_full_unstemmed An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title_short An effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
title_sort effective detachment system for human induced pluripotent stem cells cultured on multilayered cultivation substrates using resonance vibrations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821886/
https://www.ncbi.nlm.nih.gov/pubmed/31666563
http://dx.doi.org/10.1038/s41598-019-51944-w
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