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A fully defined static suspension culture system for large-scale human embryonic stem cell production
Human embryonic stem cells (hESCs) play an important role in regenerative medicine due to their potential to differentiate into various functional cells. However, the conventional adherent culture system poses challenges to mass production of high-quality hESCs. Though scientists have made many atte...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117302/ https://www.ncbi.nlm.nih.gov/pubmed/30166524 http://dx.doi.org/10.1038/s41419-018-0863-8 |
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author | Li, Xia Ma, Ruoyu Gu, Qi Liang, Lingmin Wang, Lei Zhang, Ying Wang, Xianning Liu, Xin Li, Zhongwen Fang, Jinhui Wu, Jun Wang, Yukai Li, Wei Hu, Baoyang Wang, Liu Zhou, Qi Hao, Jie |
author_facet | Li, Xia Ma, Ruoyu Gu, Qi Liang, Lingmin Wang, Lei Zhang, Ying Wang, Xianning Liu, Xin Li, Zhongwen Fang, Jinhui Wu, Jun Wang, Yukai Li, Wei Hu, Baoyang Wang, Liu Zhou, Qi Hao, Jie |
author_sort | Li, Xia |
collection | PubMed |
description | Human embryonic stem cells (hESCs) play an important role in regenerative medicine due to their potential to differentiate into various functional cells. However, the conventional adherent culture system poses challenges to mass production of high-quality hESCs. Though scientists have made many attempts to establish a robust and economical hESC suspension culture system, there are existing limitations, including suboptimal passage methods and shear force caused by dynamic stirring. Here, we report on an efficient large-scale culture system, which enables long-term, GMP grade, single-cell inoculation, and serial expansion of hESCs with a yield of about 1.5 × 10(9) cells per 1.5-L culture, while maintaining good pluripotency. The suspension culture system was enlarged gradually from a 100-mm dish to a 1.8-L culture bag with methylcellulose involvement to avoid sphere fusion. Under the optimal experimental protocol, this 3D system resolves current problems that limit mass production and clinical application of hESCs, and thus can be used in commercial-level hESC production for cell therapy and pharmaceutics screening in the future. |
format | Online Article Text |
id | pubmed-6117302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61173022018-08-31 A fully defined static suspension culture system for large-scale human embryonic stem cell production Li, Xia Ma, Ruoyu Gu, Qi Liang, Lingmin Wang, Lei Zhang, Ying Wang, Xianning Liu, Xin Li, Zhongwen Fang, Jinhui Wu, Jun Wang, Yukai Li, Wei Hu, Baoyang Wang, Liu Zhou, Qi Hao, Jie Cell Death Dis Article Human embryonic stem cells (hESCs) play an important role in regenerative medicine due to their potential to differentiate into various functional cells. However, the conventional adherent culture system poses challenges to mass production of high-quality hESCs. Though scientists have made many attempts to establish a robust and economical hESC suspension culture system, there are existing limitations, including suboptimal passage methods and shear force caused by dynamic stirring. Here, we report on an efficient large-scale culture system, which enables long-term, GMP grade, single-cell inoculation, and serial expansion of hESCs with a yield of about 1.5 × 10(9) cells per 1.5-L culture, while maintaining good pluripotency. The suspension culture system was enlarged gradually from a 100-mm dish to a 1.8-L culture bag with methylcellulose involvement to avoid sphere fusion. Under the optimal experimental protocol, this 3D system resolves current problems that limit mass production and clinical application of hESCs, and thus can be used in commercial-level hESC production for cell therapy and pharmaceutics screening in the future. Nature Publishing Group UK 2018-08-30 /pmc/articles/PMC6117302/ /pubmed/30166524 http://dx.doi.org/10.1038/s41419-018-0863-8 Text en © The Author(s) 2018 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, Xia Ma, Ruoyu Gu, Qi Liang, Lingmin Wang, Lei Zhang, Ying Wang, Xianning Liu, Xin Li, Zhongwen Fang, Jinhui Wu, Jun Wang, Yukai Li, Wei Hu, Baoyang Wang, Liu Zhou, Qi Hao, Jie A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title | A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title_full | A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title_fullStr | A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title_full_unstemmed | A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title_short | A fully defined static suspension culture system for large-scale human embryonic stem cell production |
title_sort | fully defined static suspension culture system for large-scale human embryonic stem cell production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117302/ https://www.ncbi.nlm.nih.gov/pubmed/30166524 http://dx.doi.org/10.1038/s41419-018-0863-8 |
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