Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells

<p>Abstract</p> <p>Background</p> <p>Mesenchymal stem cells (MSC) are pluripotent cells, present in the bone marrow and other tissues that can differentiate into cells of all germ layers and may be involved in tissue maintenance and repair in adult organisms. Because of...

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Main Authors: Webster Keith A, Yu Hong, Shehadeh Lina A, Wilson Amber
Format: Article
Language:English
Published: BMC 2010-04-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/11/229
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spelling doaj-d3d69254f1b2441abd1d81d21e52aaaf2020-11-24T21:01:38ZengBMCBMC Genomics1471-21642010-04-0111122910.1186/1471-2164-11-229Age-related molecular genetic changes of murine bone marrow mesenchymal stem cellsWebster Keith AYu HongShehadeh Lina AWilson Amber<p>Abstract</p> <p>Background</p> <p>Mesenchymal stem cells (MSC) are pluripotent cells, present in the bone marrow and other tissues that can differentiate into cells of all germ layers and may be involved in tissue maintenance and repair in adult organisms. Because of their plasticity and accessibility these cells are also prime candidates for regenerative medicine. The contribution of stem cell aging to organismal aging is under debate and one theory is that reparative processes deteriorate as a consequence of stem cell aging and/or decrease in number. Age has been linked with changes in osteogenic and adipogenic potential of MSCs.</p> <p>Results</p> <p>Here we report on changes in global gene expression of cultured MSCs isolated from the bone marrow of mice at ages 2, 8, and 26-months. Microarray analyses revealed significant changes in the expression of more than 8000 genes with stage-specific changes of multiple differentiation, cell cycle and growth factor genes. Key markers of adipogenesis including lipoprotein lipase, FABP4, and Itm2a displayed age-dependent declines. Expression of the master cell cycle regulators p53 and p21 and growth factors HGF and VEGF also declined significantly at 26 months. These changes were evident despite multiple cell divisions in vitro after bone marrow isolation.</p> <p>Conclusions</p> <p>The results suggest that MSCs are subject to molecular genetic changes during aging that are conserved during passage in culture. These changes may affect the physiological functions and the potential of autologous MSCs for stem cell therapy.</p> http://www.biomedcentral.com/1471-2164/11/229
collection DOAJ
language English
format Article
sources DOAJ
author Webster Keith A
Yu Hong
Shehadeh Lina A
Wilson Amber
spellingShingle Webster Keith A
Yu Hong
Shehadeh Lina A
Wilson Amber
Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
BMC Genomics
author_facet Webster Keith A
Yu Hong
Shehadeh Lina A
Wilson Amber
author_sort Webster Keith A
title Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
title_short Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
title_full Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
title_fullStr Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
title_full_unstemmed Age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
title_sort age-related molecular genetic changes of murine bone marrow mesenchymal stem cells
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2010-04-01
description <p>Abstract</p> <p>Background</p> <p>Mesenchymal stem cells (MSC) are pluripotent cells, present in the bone marrow and other tissues that can differentiate into cells of all germ layers and may be involved in tissue maintenance and repair in adult organisms. Because of their plasticity and accessibility these cells are also prime candidates for regenerative medicine. The contribution of stem cell aging to organismal aging is under debate and one theory is that reparative processes deteriorate as a consequence of stem cell aging and/or decrease in number. Age has been linked with changes in osteogenic and adipogenic potential of MSCs.</p> <p>Results</p> <p>Here we report on changes in global gene expression of cultured MSCs isolated from the bone marrow of mice at ages 2, 8, and 26-months. Microarray analyses revealed significant changes in the expression of more than 8000 genes with stage-specific changes of multiple differentiation, cell cycle and growth factor genes. Key markers of adipogenesis including lipoprotein lipase, FABP4, and Itm2a displayed age-dependent declines. Expression of the master cell cycle regulators p53 and p21 and growth factors HGF and VEGF also declined significantly at 26 months. These changes were evident despite multiple cell divisions in vitro after bone marrow isolation.</p> <p>Conclusions</p> <p>The results suggest that MSCs are subject to molecular genetic changes during aging that are conserved during passage in culture. These changes may affect the physiological functions and the potential of autologous MSCs for stem cell therapy.</p>
url http://www.biomedcentral.com/1471-2164/11/229
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