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Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents

BACKGROUND: The rapid clinical translation of mesenchymal stem cells (MSC) has resulted in the development of cell-based strategies for multiple indications. Unfortunately one major barrier to widespread implementation of MSC-based therapies is the limited supply of fetal calf serum (FCS) used to ex...

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Autores principales: Riordan, Neil H, Madrigal, Marialaura, Reneau, Jason, de Cupeiro, Kathya, Jiménez, Natalia, Ruiz, Sergio, Sanchez, Nelsy, Ichim, Thomas E, Silva, Francisco, Patel, Amit N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504159/
https://www.ncbi.nlm.nih.gov/pubmed/26183703
http://dx.doi.org/10.1186/s12967-015-0561-6
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author Riordan, Neil H
Madrigal, Marialaura
Reneau, Jason
de Cupeiro, Kathya
Jiménez, Natalia
Ruiz, Sergio
Sanchez, Nelsy
Ichim, Thomas E
Silva, Francisco
Patel, Amit N
author_facet Riordan, Neil H
Madrigal, Marialaura
Reneau, Jason
de Cupeiro, Kathya
Jiménez, Natalia
Ruiz, Sergio
Sanchez, Nelsy
Ichim, Thomas E
Silva, Francisco
Patel, Amit N
author_sort Riordan, Neil H
collection PubMed
description BACKGROUND: The rapid clinical translation of mesenchymal stem cells (MSC) has resulted in the development of cell-based strategies for multiple indications. Unfortunately one major barrier to widespread implementation of MSC-based therapies is the limited supply of fetal calf serum (FCS) used to expand cells to therapeutic numbers. Additionally, the xenogeneic element of fetal calf serum has been previously demonstrated to stimulate antibody mediated reactions and in some cases sensitization leading to anaphylaxis. METHOD: XcytePLUS™ media, a human platelet lysate based product, was used to supplement the culture medium at 5, 7.5 and 10% and compared to fetal calf serum at 10%, for human umbilical cord MSC expansion. Properties of the expanded cells were investigated. RESULTS: This study demonstrated equivalent or superior effects of human platelet lysate compared to standard FCS supplemented media, based on doubling rate, without loss of identity or function, as demonstrated with flow cytometry characterization. Differentiation into osteocytes, adipocytes and chondrocytes was comparable from cells expanded in either media supplement. CONCLUSIONS: These data support the implementation of human platelet lysate supplemented media as an alternative to xenogeneic containing preparations which may lead to safer MSC products with therapeutic uses.
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spelling pubmed-45041592015-07-17 Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents Riordan, Neil H Madrigal, Marialaura Reneau, Jason de Cupeiro, Kathya Jiménez, Natalia Ruiz, Sergio Sanchez, Nelsy Ichim, Thomas E Silva, Francisco Patel, Amit N J Transl Med Research BACKGROUND: The rapid clinical translation of mesenchymal stem cells (MSC) has resulted in the development of cell-based strategies for multiple indications. Unfortunately one major barrier to widespread implementation of MSC-based therapies is the limited supply of fetal calf serum (FCS) used to expand cells to therapeutic numbers. Additionally, the xenogeneic element of fetal calf serum has been previously demonstrated to stimulate antibody mediated reactions and in some cases sensitization leading to anaphylaxis. METHOD: XcytePLUS™ media, a human platelet lysate based product, was used to supplement the culture medium at 5, 7.5 and 10% and compared to fetal calf serum at 10%, for human umbilical cord MSC expansion. Properties of the expanded cells were investigated. RESULTS: This study demonstrated equivalent or superior effects of human platelet lysate compared to standard FCS supplemented media, based on doubling rate, without loss of identity or function, as demonstrated with flow cytometry characterization. Differentiation into osteocytes, adipocytes and chondrocytes was comparable from cells expanded in either media supplement. CONCLUSIONS: These data support the implementation of human platelet lysate supplemented media as an alternative to xenogeneic containing preparations which may lead to safer MSC products with therapeutic uses. BioMed Central 2015-07-17 /pmc/articles/PMC4504159/ /pubmed/26183703 http://dx.doi.org/10.1186/s12967-015-0561-6 Text en © Riordan et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Riordan, Neil H
Madrigal, Marialaura
Reneau, Jason
de Cupeiro, Kathya
Jiménez, Natalia
Ruiz, Sergio
Sanchez, Nelsy
Ichim, Thomas E
Silva, Francisco
Patel, Amit N
Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title_full Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title_fullStr Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title_full_unstemmed Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title_short Scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
title_sort scalable efficient expansion of mesenchymal stem cells in xeno free media using commercially available reagents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504159/
https://www.ncbi.nlm.nih.gov/pubmed/26183703
http://dx.doi.org/10.1186/s12967-015-0561-6
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