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Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells

Despite recent progress in the preparation of feeder cells for human induced pluripotent stem cells (hiPSCs), there remain issues which limit the acquisition of feeder cells in large scale. Approaches for obtaining feeder cells quickly on a large scale are in immediate need. To reach this goal, we e...

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Autores principales: Li, Pengdong, Wang, Shichao, Zhan, Lixiang, He, Xia, Chi, Guangfan, Lv, Shuang, Xu, Ziran, Xia, Yuhan, Teng, Shuzhi, Li, Lisha, Li, Yulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612988/
https://www.ncbi.nlm.nih.gov/pubmed/28947775
http://dx.doi.org/10.1038/s41598-017-10428-5
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author Li, Pengdong
Wang, Shichao
Zhan, Lixiang
He, Xia
Chi, Guangfan
Lv, Shuang
Xu, Ziran
Xia, Yuhan
Teng, Shuzhi
Li, Lisha
Li, Yulin
author_facet Li, Pengdong
Wang, Shichao
Zhan, Lixiang
He, Xia
Chi, Guangfan
Lv, Shuang
Xu, Ziran
Xia, Yuhan
Teng, Shuzhi
Li, Lisha
Li, Yulin
author_sort Li, Pengdong
collection PubMed
description Despite recent progress in the preparation of feeder cells for human induced pluripotent stem cells (hiPSCs), there remain issues which limit the acquisition of feeder cells in large scale. Approaches for obtaining feeder cells quickly on a large scale are in immediate need. To reach this goal, we established suspension-adhesion method (SAM) and three-dimensional (3D) suspension method (3DSM). In SAM, mouse embryonic fibroblast (MEF) growth were fully inhibited by 10 μg/ml mitomycin-C (MMC) in 0.5 hours, and the feeder cells generated display higher adherent and recovery rates as well as longer survival time compared to conventional method (CM). 3DSM, an optimized method of SAM in which MEFs were cultured and MMC treated in suspension, was developed to lower the costs and workload using CELLSPIN System. The yield of feeder cells is several times the yield of SAM while the adherent and recovery rates and the capacity of supporting hiPSCs growth were not sacrificed. Hence, 3DSM is an economical and easy way to generate large-scale feeder cells for hiPSCs cultures.
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spelling pubmed-56129882017-10-11 Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells Li, Pengdong Wang, Shichao Zhan, Lixiang He, Xia Chi, Guangfan Lv, Shuang Xu, Ziran Xia, Yuhan Teng, Shuzhi Li, Lisha Li, Yulin Sci Rep Article Despite recent progress in the preparation of feeder cells for human induced pluripotent stem cells (hiPSCs), there remain issues which limit the acquisition of feeder cells in large scale. Approaches for obtaining feeder cells quickly on a large scale are in immediate need. To reach this goal, we established suspension-adhesion method (SAM) and three-dimensional (3D) suspension method (3DSM). In SAM, mouse embryonic fibroblast (MEF) growth were fully inhibited by 10 μg/ml mitomycin-C (MMC) in 0.5 hours, and the feeder cells generated display higher adherent and recovery rates as well as longer survival time compared to conventional method (CM). 3DSM, an optimized method of SAM in which MEFs were cultured and MMC treated in suspension, was developed to lower the costs and workload using CELLSPIN System. The yield of feeder cells is several times the yield of SAM while the adherent and recovery rates and the capacity of supporting hiPSCs growth were not sacrificed. Hence, 3DSM is an economical and easy way to generate large-scale feeder cells for hiPSCs cultures. Nature Publishing Group UK 2017-09-25 /pmc/articles/PMC5612988/ /pubmed/28947775 http://dx.doi.org/10.1038/s41598-017-10428-5 Text en © The Author(s) 2017 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
Li, Pengdong
Wang, Shichao
Zhan, Lixiang
He, Xia
Chi, Guangfan
Lv, Shuang
Xu, Ziran
Xia, Yuhan
Teng, Shuzhi
Li, Lisha
Li, Yulin
Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title_full Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title_fullStr Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title_full_unstemmed Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title_short Efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
title_sort efficient feeder cells preparation system for large-scale preparation and application of induced pluripotent stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612988/
https://www.ncbi.nlm.nih.gov/pubmed/28947775
http://dx.doi.org/10.1038/s41598-017-10428-5
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