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Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation
BACKGROUND: Human adipose tissue is an ideal autologous source of mesenchymal stem cells (MSCs) for various regenerative medicine and tissue engineering strategies. Aged patients are one of the primary target populations for many promising applications. It has long been known that advanced age is ne...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895760/ https://www.ncbi.nlm.nih.gov/pubmed/24397850 http://dx.doi.org/10.1186/1479-5876-12-8 |
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author | Choudhery, Mahmood S Badowski, Michael Muise, Angela Pierce, John Harris, David T |
author_facet | Choudhery, Mahmood S Badowski, Michael Muise, Angela Pierce, John Harris, David T |
author_sort | Choudhery, Mahmood S |
collection | PubMed |
description | BACKGROUND: Human adipose tissue is an ideal autologous source of mesenchymal stem cells (MSCs) for various regenerative medicine and tissue engineering strategies. Aged patients are one of the primary target populations for many promising applications. It has long been known that advanced age is negatively correlated with an organism’s reparative and regenerative potential, but little and conflicting information is available about the effects of age on the quality of human adipose tissue derived MSCs (hAT-MSCs). METHODS: To study the influence of age, the expansion and in vitro differentiation potential of hAT-MSCs from young (<30 years), adult (35-50 years) and aged (>60 years) individuals were investigated. MSCs were characterized for expression of the genes p16(INK4a) and p21 along with measurements of population doublings (PD), superoxide dismutase (SOD) activity, cellular senescence and differentiation potential. RESULTS: Aged MSCs displayed senescent features when compared with cells isolated from young donors, concomitant with reduced viability and proliferation. These features were also associated with significantly reduced differentiation potential in aged MSCs compared to young MSCs. CONCLUSIONS: In conclusion, advancing age negatively impacts stem cell function and such age related alterations may be detrimental for successful stem cell therapies. |
format | Online Article Text |
id | pubmed-3895760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38957602014-01-29 Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation Choudhery, Mahmood S Badowski, Michael Muise, Angela Pierce, John Harris, David T J Transl Med Research BACKGROUND: Human adipose tissue is an ideal autologous source of mesenchymal stem cells (MSCs) for various regenerative medicine and tissue engineering strategies. Aged patients are one of the primary target populations for many promising applications. It has long been known that advanced age is negatively correlated with an organism’s reparative and regenerative potential, but little and conflicting information is available about the effects of age on the quality of human adipose tissue derived MSCs (hAT-MSCs). METHODS: To study the influence of age, the expansion and in vitro differentiation potential of hAT-MSCs from young (<30 years), adult (35-50 years) and aged (>60 years) individuals were investigated. MSCs were characterized for expression of the genes p16(INK4a) and p21 along with measurements of population doublings (PD), superoxide dismutase (SOD) activity, cellular senescence and differentiation potential. RESULTS: Aged MSCs displayed senescent features when compared with cells isolated from young donors, concomitant with reduced viability and proliferation. These features were also associated with significantly reduced differentiation potential in aged MSCs compared to young MSCs. CONCLUSIONS: In conclusion, advancing age negatively impacts stem cell function and such age related alterations may be detrimental for successful stem cell therapies. BioMed Central 2014-01-07 /pmc/articles/PMC3895760/ /pubmed/24397850 http://dx.doi.org/10.1186/1479-5876-12-8 Text en Copyright © 2014 Choudhery et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Choudhery, Mahmood S Badowski, Michael Muise, Angela Pierce, John Harris, David T Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title | Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title_full | Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title_fullStr | Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title_full_unstemmed | Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title_short | Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
title_sort | donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895760/ https://www.ncbi.nlm.nih.gov/pubmed/24397850 http://dx.doi.org/10.1186/1479-5876-12-8 |
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