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Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells

BACKGROUND: Bone marrow-derived mesenchymal stem cells (BMSCs) are a widely researched adult stem cell population capable of differentiation into various lineages. Because many promising applications of tissue engineering require cell expansion following harvest and involve the treatment of diseases...

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Autores principales: Kretlow, James D, Jin, Yu-Qing, Liu, Wei, Zhang, Wen Jie, Hong, Tan-Hui, Zhou, Guangdong, Baggett, L Scott, Mikos, Antonios G, Cao, Yilin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584028/
https://www.ncbi.nlm.nih.gov/pubmed/18957087
http://dx.doi.org/10.1186/1471-2121-9-60
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author Kretlow, James D
Jin, Yu-Qing
Liu, Wei
Zhang, Wen Jie
Hong, Tan-Hui
Zhou, Guangdong
Baggett, L Scott
Mikos, Antonios G
Cao, Yilin
author_facet Kretlow, James D
Jin, Yu-Qing
Liu, Wei
Zhang, Wen Jie
Hong, Tan-Hui
Zhou, Guangdong
Baggett, L Scott
Mikos, Antonios G
Cao, Yilin
author_sort Kretlow, James D
collection PubMed
description BACKGROUND: Bone marrow-derived mesenchymal stem cells (BMSCs) are a widely researched adult stem cell population capable of differentiation into various lineages. Because many promising applications of tissue engineering require cell expansion following harvest and involve the treatment of diseases and conditions found in an aging population, the effect of donor age and ex vivo handling must be understood in order to develop clinical techniques and therapeutics based on these cells. Furthermore, there currently exists little understanding as to how these two factors may be influenced by one another. RESULTS: Differences in the adipogenic, chondrogenic, and osteogenic differentiation capacity of murine MSCs harvested from donor animals of different age and number of passages of these cells were observed. Cells from younger donors adhered to tissue culture polystyrene better and proliferated in greater number than those from older animals. Chondrogenic and osteogenic potential decreased with age for each group, and adipogenic differentiation decreased only in cells from the oldest donors. Significant decreases in differentiation potentials due to passage were observed as well for osteogenesis of BMSCs from the youngest donors and chondrogenesis of the cells from the oldest donors. CONCLUSION: Both increasing age and the number of passages have lineage dependent effects on BMSC differentiation potential. Furthermore, there is an obvious interplay between donor age and cell passage that in the future must be accounted for when developing cell-based therapies for clinical use.
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spelling pubmed-25840282008-11-18 Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells Kretlow, James D Jin, Yu-Qing Liu, Wei Zhang, Wen Jie Hong, Tan-Hui Zhou, Guangdong Baggett, L Scott Mikos, Antonios G Cao, Yilin BMC Cell Biol Research Article BACKGROUND: Bone marrow-derived mesenchymal stem cells (BMSCs) are a widely researched adult stem cell population capable of differentiation into various lineages. Because many promising applications of tissue engineering require cell expansion following harvest and involve the treatment of diseases and conditions found in an aging population, the effect of donor age and ex vivo handling must be understood in order to develop clinical techniques and therapeutics based on these cells. Furthermore, there currently exists little understanding as to how these two factors may be influenced by one another. RESULTS: Differences in the adipogenic, chondrogenic, and osteogenic differentiation capacity of murine MSCs harvested from donor animals of different age and number of passages of these cells were observed. Cells from younger donors adhered to tissue culture polystyrene better and proliferated in greater number than those from older animals. Chondrogenic and osteogenic potential decreased with age for each group, and adipogenic differentiation decreased only in cells from the oldest donors. Significant decreases in differentiation potentials due to passage were observed as well for osteogenesis of BMSCs from the youngest donors and chondrogenesis of the cells from the oldest donors. CONCLUSION: Both increasing age and the number of passages have lineage dependent effects on BMSC differentiation potential. Furthermore, there is an obvious interplay between donor age and cell passage that in the future must be accounted for when developing cell-based therapies for clinical use. BioMed Central 2008-10-28 /pmc/articles/PMC2584028/ /pubmed/18957087 http://dx.doi.org/10.1186/1471-2121-9-60 Text en Copyright © 2008 Kretlow 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.
spellingShingle Research Article
Kretlow, James D
Jin, Yu-Qing
Liu, Wei
Zhang, Wen Jie
Hong, Tan-Hui
Zhou, Guangdong
Baggett, L Scott
Mikos, Antonios G
Cao, Yilin
Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title_full Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title_fullStr Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title_full_unstemmed Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title_short Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
title_sort donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584028/
https://www.ncbi.nlm.nih.gov/pubmed/18957087
http://dx.doi.org/10.1186/1471-2121-9-60
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