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Transplantation of mesenchymal stem cells from young donors delays aging in mice

Increasing evidence suggests that the loss of functional stem cells may be important in the aging process. Our experiments were originally aimed at testing the idea that, in the specific case of age-related osteoporosis, declining function of osteogenic precursor cells might be at least partially re...

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Autores principales: Shen, Jinhui, Tsai, Yi-Ting, DiMarco, Nancy M., Long, Michael A., Sun, Xiankai, Tang, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216554/
https://www.ncbi.nlm.nih.gov/pubmed/22355586
http://dx.doi.org/10.1038/srep00067
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author Shen, Jinhui
Tsai, Yi-Ting
DiMarco, Nancy M.
Long, Michael A.
Sun, Xiankai
Tang, Liping
author_facet Shen, Jinhui
Tsai, Yi-Ting
DiMarco, Nancy M.
Long, Michael A.
Sun, Xiankai
Tang, Liping
author_sort Shen, Jinhui
collection PubMed
description Increasing evidence suggests that the loss of functional stem cells may be important in the aging process. Our experiments were originally aimed at testing the idea that, in the specific case of age-related osteoporosis, declining function of osteogenic precursor cells might be at least partially responsible. To test this, aging female mice were transplanted with mesenchymal stem cells from aged or young male donors. We find that transplantation of young mesenchymal stem cells significantly slows the loss of bone density and, surprisingly, prolongs the life span of old mice. These observations lend further support to the idea that age-related diminution of stem cell number or function may play a critical role in age-related loss of bone density in aging animals and may be one determinant of overall longevity.
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spelling pubmed-32165542011-12-22 Transplantation of mesenchymal stem cells from young donors delays aging in mice Shen, Jinhui Tsai, Yi-Ting DiMarco, Nancy M. Long, Michael A. Sun, Xiankai Tang, Liping Sci Rep Article Increasing evidence suggests that the loss of functional stem cells may be important in the aging process. Our experiments were originally aimed at testing the idea that, in the specific case of age-related osteoporosis, declining function of osteogenic precursor cells might be at least partially responsible. To test this, aging female mice were transplanted with mesenchymal stem cells from aged or young male donors. We find that transplantation of young mesenchymal stem cells significantly slows the loss of bone density and, surprisingly, prolongs the life span of old mice. These observations lend further support to the idea that age-related diminution of stem cell number or function may play a critical role in age-related loss of bone density in aging animals and may be one determinant of overall longevity. Nature Publishing Group 2011-08-18 /pmc/articles/PMC3216554/ /pubmed/22355586 http://dx.doi.org/10.1038/srep00067 Text en Copyright © 2011, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Shen, Jinhui
Tsai, Yi-Ting
DiMarco, Nancy M.
Long, Michael A.
Sun, Xiankai
Tang, Liping
Transplantation of mesenchymal stem cells from young donors delays aging in mice
title Transplantation of mesenchymal stem cells from young donors delays aging in mice
title_full Transplantation of mesenchymal stem cells from young donors delays aging in mice
title_fullStr Transplantation of mesenchymal stem cells from young donors delays aging in mice
title_full_unstemmed Transplantation of mesenchymal stem cells from young donors delays aging in mice
title_short Transplantation of mesenchymal stem cells from young donors delays aging in mice
title_sort transplantation of mesenchymal stem cells from young donors delays aging in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216554/
https://www.ncbi.nlm.nih.gov/pubmed/22355586
http://dx.doi.org/10.1038/srep00067
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