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Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media
Due to their immunosuppressive properties, mesenchymal stem cells (MSC) have been evaluated for the treatment of immunological diseases. However, the animal-derived growth supplements utilized for MSC manufacturing may lead to clinical complications. Characterization of alternative media formulation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643287/ https://www.ncbi.nlm.nih.gov/pubmed/26564250 http://dx.doi.org/10.1038/srep16570 |
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author | Oikonomopoulos, Angelos van Deen, Welmoed K. Manansala, Aida-Rae Lacey, Precious N. Tomakili, Tamera A. Ziman, Alyssa Hommes, Daniel W. |
author_facet | Oikonomopoulos, Angelos van Deen, Welmoed K. Manansala, Aida-Rae Lacey, Precious N. Tomakili, Tamera A. Ziman, Alyssa Hommes, Daniel W. |
author_sort | Oikonomopoulos, Angelos |
collection | PubMed |
description | Due to their immunosuppressive properties, mesenchymal stem cells (MSC) have been evaluated for the treatment of immunological diseases. However, the animal-derived growth supplements utilized for MSC manufacturing may lead to clinical complications. Characterization of alternative media formulations is imperative for MSC therapeutic application. Human BMMSC and AdMSC were expanded in media supplemented with either human platelet lysates (HPL), serum-free media/xeno-free FDA-approved culture medium (SFM/XF), or fetal bovine serum (FBS) and the effects on their properties were investigated. The immunophenotype of resting and IFN-γ primed BMMSC and AdMSC remained unaltered in all media. Both HPL and SFM/XF increased the proliferation of BMMSC and AdMSC. Expansion of BMMSC and AdMSC in HPL increased their differentiation, compared to SFM/XF and FBS. Resting BMMSC and AdMSC, expanded in FBS or SFM/XF, demonstrated potent immunosuppressive properties in both non-primed and IFN-γ primed conditions, whereas HPL-expanded MSC exhibited diminished immunosuppressive properties. Finally, IFN-γ primed BMMSC and AdMSC expanded in SFM/XF and HPL expressed attenuated levels of IDO-1 compared to FBS. Herein, we provide strong evidence supporting the use of the FDA-approved SFM/XF medium, in contrast to the HPL medium, for the expansion of MSC towards therapeutic applications. |
format | Online Article Text |
id | pubmed-4643287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46432872015-11-20 Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media Oikonomopoulos, Angelos van Deen, Welmoed K. Manansala, Aida-Rae Lacey, Precious N. Tomakili, Tamera A. Ziman, Alyssa Hommes, Daniel W. Sci Rep Article Due to their immunosuppressive properties, mesenchymal stem cells (MSC) have been evaluated for the treatment of immunological diseases. However, the animal-derived growth supplements utilized for MSC manufacturing may lead to clinical complications. Characterization of alternative media formulations is imperative for MSC therapeutic application. Human BMMSC and AdMSC were expanded in media supplemented with either human platelet lysates (HPL), serum-free media/xeno-free FDA-approved culture medium (SFM/XF), or fetal bovine serum (FBS) and the effects on their properties were investigated. The immunophenotype of resting and IFN-γ primed BMMSC and AdMSC remained unaltered in all media. Both HPL and SFM/XF increased the proliferation of BMMSC and AdMSC. Expansion of BMMSC and AdMSC in HPL increased their differentiation, compared to SFM/XF and FBS. Resting BMMSC and AdMSC, expanded in FBS or SFM/XF, demonstrated potent immunosuppressive properties in both non-primed and IFN-γ primed conditions, whereas HPL-expanded MSC exhibited diminished immunosuppressive properties. Finally, IFN-γ primed BMMSC and AdMSC expanded in SFM/XF and HPL expressed attenuated levels of IDO-1 compared to FBS. Herein, we provide strong evidence supporting the use of the FDA-approved SFM/XF medium, in contrast to the HPL medium, for the expansion of MSC towards therapeutic applications. Nature Publishing Group 2015-11-13 /pmc/articles/PMC4643287/ /pubmed/26564250 http://dx.doi.org/10.1038/srep16570 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Oikonomopoulos, Angelos van Deen, Welmoed K. Manansala, Aida-Rae Lacey, Precious N. Tomakili, Tamera A. Ziman, Alyssa Hommes, Daniel W. Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title | Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title_full | Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title_fullStr | Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title_full_unstemmed | Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title_short | Optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
title_sort | optimization of human mesenchymal stem cell manufacturing: the effects of animal/xeno-free media |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643287/ https://www.ncbi.nlm.nih.gov/pubmed/26564250 http://dx.doi.org/10.1038/srep16570 |
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