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Establishing Criteria for Human Mesenchymal Stem Cell Potency

This study sought to identify critical determinants of mesenchymal stem cell (MSC) potency using in vitro and in vivo attributes of cells isolated from the bone marrow of age‐ and sex‐matched donors. Adherence to plastic was not indicative of potency, yet capacity for long‐term expansion in vitro va...

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Autores principales: Samsonraj, Rebekah M., Rai, Bina, Sathiyanathan, Padmapriya, Puan, Kia Joo, Rötzschke, Olaf, Hui, James H., Raghunath, Michael, Stanton, Lawrence W., Nurcombe, Victor, Cool, Simon M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363381/
https://www.ncbi.nlm.nih.gov/pubmed/25752682
http://dx.doi.org/10.1002/stem.1982
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author Samsonraj, Rebekah M.
Rai, Bina
Sathiyanathan, Padmapriya
Puan, Kia Joo
Rötzschke, Olaf
Hui, James H.
Raghunath, Michael
Stanton, Lawrence W.
Nurcombe, Victor
Cool, Simon M.
author_facet Samsonraj, Rebekah M.
Rai, Bina
Sathiyanathan, Padmapriya
Puan, Kia Joo
Rötzschke, Olaf
Hui, James H.
Raghunath, Michael
Stanton, Lawrence W.
Nurcombe, Victor
Cool, Simon M.
author_sort Samsonraj, Rebekah M.
collection PubMed
description This study sought to identify critical determinants of mesenchymal stem cell (MSC) potency using in vitro and in vivo attributes of cells isolated from the bone marrow of age‐ and sex‐matched donors. Adherence to plastic was not indicative of potency, yet capacity for long‐term expansion in vitro varied considerably between donors, allowing the grouping of MSCs from the donors into either those with high‐growth capacity or low‐growth capacity. Using this grouping strategy, high‐growth capacity MSCs were smaller in size, had greater colony‐forming efficiency, and had longer telomeres. Cell‐surface biomarker analysis revealed that the International Society for Cellular Therapy (ISCT) criteria did not distinguish between high‐growth capacity and low‐growth capacity MSCs, whereas STRO‐1 and platelet‐derived growth factor receptor alpha were preferentially expressed on high‐growth capacity MSCs. These cells also had the highest mean expression of the mRNA transcripts TWIST‐1 and DERMO‐1. Irrespective of these differences, both groups of donor MSCs produced similar levels of key growth factors and cytokines involved in tissue regeneration and were capable of multilineage differentiation. However, high‐growth capacity MSCs produced approximately double the volume of mineralized tissue compared to low‐growth capacity MSCs when assessed for ectopic bone‐forming ability. The additional phenotypic criteria presented in this study when combined with the existing ISCT minimum criteria and working proposal will permit an improved assessment of MSC potency and provide a basis for establishing the quality of MSCs prior to their therapeutic application. Stem Cells 2015;33:1878–1891
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spelling pubmed-53633812017-04-06 Establishing Criteria for Human Mesenchymal Stem Cell Potency Samsonraj, Rebekah M. Rai, Bina Sathiyanathan, Padmapriya Puan, Kia Joo Rötzschke, Olaf Hui, James H. Raghunath, Michael Stanton, Lawrence W. Nurcombe, Victor Cool, Simon M. Stem Cells Translational and Clinical Research This study sought to identify critical determinants of mesenchymal stem cell (MSC) potency using in vitro and in vivo attributes of cells isolated from the bone marrow of age‐ and sex‐matched donors. Adherence to plastic was not indicative of potency, yet capacity for long‐term expansion in vitro varied considerably between donors, allowing the grouping of MSCs from the donors into either those with high‐growth capacity or low‐growth capacity. Using this grouping strategy, high‐growth capacity MSCs were smaller in size, had greater colony‐forming efficiency, and had longer telomeres. Cell‐surface biomarker analysis revealed that the International Society for Cellular Therapy (ISCT) criteria did not distinguish between high‐growth capacity and low‐growth capacity MSCs, whereas STRO‐1 and platelet‐derived growth factor receptor alpha were preferentially expressed on high‐growth capacity MSCs. These cells also had the highest mean expression of the mRNA transcripts TWIST‐1 and DERMO‐1. Irrespective of these differences, both groups of donor MSCs produced similar levels of key growth factors and cytokines involved in tissue regeneration and were capable of multilineage differentiation. However, high‐growth capacity MSCs produced approximately double the volume of mineralized tissue compared to low‐growth capacity MSCs when assessed for ectopic bone‐forming ability. The additional phenotypic criteria presented in this study when combined with the existing ISCT minimum criteria and working proposal will permit an improved assessment of MSC potency and provide a basis for establishing the quality of MSCs prior to their therapeutic application. Stem Cells 2015;33:1878–1891 John Wiley and Sons Inc. 2015-06 2015-05-21 /pmc/articles/PMC5363381/ /pubmed/25752682 http://dx.doi.org/10.1002/stem.1982 Text en © 2015 The Authors STEM CELLS published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Translational and Clinical Research
Samsonraj, Rebekah M.
Rai, Bina
Sathiyanathan, Padmapriya
Puan, Kia Joo
Rötzschke, Olaf
Hui, James H.
Raghunath, Michael
Stanton, Lawrence W.
Nurcombe, Victor
Cool, Simon M.
Establishing Criteria for Human Mesenchymal Stem Cell Potency
title Establishing Criteria for Human Mesenchymal Stem Cell Potency
title_full Establishing Criteria for Human Mesenchymal Stem Cell Potency
title_fullStr Establishing Criteria for Human Mesenchymal Stem Cell Potency
title_full_unstemmed Establishing Criteria for Human Mesenchymal Stem Cell Potency
title_short Establishing Criteria for Human Mesenchymal Stem Cell Potency
title_sort establishing criteria for human mesenchymal stem cell potency
topic Translational and Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363381/
https://www.ncbi.nlm.nih.gov/pubmed/25752682
http://dx.doi.org/10.1002/stem.1982
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