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A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells

Human pluripotent stem cells (hPSCs) present an unprecedented opportunity to advance human health by offering an alternative and renewable cell resource for cellular therapeutics and regenerative medicine. The present demand for high quality hPSCs for use in both research and clinical studies unders...

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Autores principales: Ahmadian Baghbaderani, Behnam, Tian, Xinghui, Scotty Cadet, Jean, Shah, Kevan, Walde, Amy, Tran, Huan, Kovarcik, Don Paul, Clarke, Diana, Fellner, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016087/
https://www.ncbi.nlm.nih.gov/pubmed/27606941
http://dx.doi.org/10.1371/journal.pone.0161229
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author Ahmadian Baghbaderani, Behnam
Tian, Xinghui
Scotty Cadet, Jean
Shah, Kevan
Walde, Amy
Tran, Huan
Kovarcik, Don Paul
Clarke, Diana
Fellner, Thomas
author_facet Ahmadian Baghbaderani, Behnam
Tian, Xinghui
Scotty Cadet, Jean
Shah, Kevan
Walde, Amy
Tran, Huan
Kovarcik, Don Paul
Clarke, Diana
Fellner, Thomas
author_sort Ahmadian Baghbaderani, Behnam
collection PubMed
description Human pluripotent stem cells (hPSCs) present an unprecedented opportunity to advance human health by offering an alternative and renewable cell resource for cellular therapeutics and regenerative medicine. The present demand for high quality hPSCs for use in both research and clinical studies underscores the need to develop technologies that will simplify the cultivation process and control variability. Here we describe the development of a robust, defined and xeno-free hPSC medium that supports reliable propagation of hPSCs and generation of human induced pluripotent stem cells (hiPSCs) from multiple somatic cell types; long-term serial subculturing of hPSCs with every-other-day (EOD) medium replacement; and banking fully characterized hPSCs. The hPSCs cultured in this medium for over 40 passages are genetically stable, retain high expression levels of the pluripotency markers TRA-1-60, TRA-1-81, Oct-3/4 and SSEA-4, and readily differentiate into ectoderm, mesoderm and endoderm. Importantly, the medium plays an integral role in establishing a cGMP-compliant process for the manufacturing of hiPSCs that can be used for generation of clinically relevant cell types for cell replacement therapy applications.
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spelling pubmed-50160872016-09-27 A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells Ahmadian Baghbaderani, Behnam Tian, Xinghui Scotty Cadet, Jean Shah, Kevan Walde, Amy Tran, Huan Kovarcik, Don Paul Clarke, Diana Fellner, Thomas PLoS One Research Article Human pluripotent stem cells (hPSCs) present an unprecedented opportunity to advance human health by offering an alternative and renewable cell resource for cellular therapeutics and regenerative medicine. The present demand for high quality hPSCs for use in both research and clinical studies underscores the need to develop technologies that will simplify the cultivation process and control variability. Here we describe the development of a robust, defined and xeno-free hPSC medium that supports reliable propagation of hPSCs and generation of human induced pluripotent stem cells (hiPSCs) from multiple somatic cell types; long-term serial subculturing of hPSCs with every-other-day (EOD) medium replacement; and banking fully characterized hPSCs. The hPSCs cultured in this medium for over 40 passages are genetically stable, retain high expression levels of the pluripotency markers TRA-1-60, TRA-1-81, Oct-3/4 and SSEA-4, and readily differentiate into ectoderm, mesoderm and endoderm. Importantly, the medium plays an integral role in establishing a cGMP-compliant process for the manufacturing of hiPSCs that can be used for generation of clinically relevant cell types for cell replacement therapy applications. Public Library of Science 2016-09-08 /pmc/articles/PMC5016087/ /pubmed/27606941 http://dx.doi.org/10.1371/journal.pone.0161229 Text en © 2016 Ahmadian Baghbaderani et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ahmadian Baghbaderani, Behnam
Tian, Xinghui
Scotty Cadet, Jean
Shah, Kevan
Walde, Amy
Tran, Huan
Kovarcik, Don Paul
Clarke, Diana
Fellner, Thomas
A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title_full A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title_fullStr A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title_full_unstemmed A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title_short A Newly Defined and Xeno-Free Culture Medium Supports Every-Other-Day Medium Replacement in the Generation and Long-Term Cultivation of Human Pluripotent Stem Cells
title_sort newly defined and xeno-free culture medium supports every-other-day medium replacement in the generation and long-term cultivation of human pluripotent stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016087/
https://www.ncbi.nlm.nih.gov/pubmed/27606941
http://dx.doi.org/10.1371/journal.pone.0161229
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