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Inflammation and mesenchymal stem cell aging

In adults, mesenchymal stromal cells contain tissue-specific multipotent stem cells, MSC, which can be found throughout the body. With advancing age, tight controls of regulatory networks, which guide MSC biology, gradually deteriorate. Aberrations within the MSC microenvironment such as chronic inf...

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Detalles Bibliográficos
Autor principal: Lepperdinger, Günter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167021/
https://www.ncbi.nlm.nih.gov/pubmed/21703839
http://dx.doi.org/10.1016/j.coi.2011.05.007
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author Lepperdinger, Günter
author_facet Lepperdinger, Günter
author_sort Lepperdinger, Günter
collection PubMed
description In adults, mesenchymal stromal cells contain tissue-specific multipotent stem cells, MSC, which can be found throughout the body. With advancing age, tight controls of regulatory networks, which guide MSC biology, gradually deteriorate. Aberrations within the MSC microenvironment such as chronic inflammation eventually lead to adverse manifestations, such as the accumulation of fat deposits in bone and muscles, impaired healing and fibrosis after severe injury, or altered hematopoiesis and autoimmunity. MSC can also specifically interact with a large variety of immune cells, and in doing so, they secrete cytoprotective and immunoregulatory molecules, which together with intercellular contacts mediate immune modulatory processes. This review comprehends the current knowledge regarding molecular mechanisms and cellular interactions that occur in stem cell niches, which are jointly shared between MSC and hematopoietic stem and progenitor cells, as well as those intracellular interdependences taking place between mesenchymal and a wide variety of hematopoietic progeny in particular T lymphocytes, which eventually perturb tissue homeostasis and immunology at advanced age.
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spelling pubmed-31670212011-10-11 Inflammation and mesenchymal stem cell aging Lepperdinger, Günter Curr Opin Immunol Article In adults, mesenchymal stromal cells contain tissue-specific multipotent stem cells, MSC, which can be found throughout the body. With advancing age, tight controls of regulatory networks, which guide MSC biology, gradually deteriorate. Aberrations within the MSC microenvironment such as chronic inflammation eventually lead to adverse manifestations, such as the accumulation of fat deposits in bone and muscles, impaired healing and fibrosis after severe injury, or altered hematopoiesis and autoimmunity. MSC can also specifically interact with a large variety of immune cells, and in doing so, they secrete cytoprotective and immunoregulatory molecules, which together with intercellular contacts mediate immune modulatory processes. This review comprehends the current knowledge regarding molecular mechanisms and cellular interactions that occur in stem cell niches, which are jointly shared between MSC and hematopoietic stem and progenitor cells, as well as those intracellular interdependences taking place between mesenchymal and a wide variety of hematopoietic progeny in particular T lymphocytes, which eventually perturb tissue homeostasis and immunology at advanced age. Elsevier 2011-08 /pmc/articles/PMC3167021/ /pubmed/21703839 http://dx.doi.org/10.1016/j.coi.2011.05.007 Text en © 2011 Elsevier Ltd. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Article
Lepperdinger, Günter
Inflammation and mesenchymal stem cell aging
title Inflammation and mesenchymal stem cell aging
title_full Inflammation and mesenchymal stem cell aging
title_fullStr Inflammation and mesenchymal stem cell aging
title_full_unstemmed Inflammation and mesenchymal stem cell aging
title_short Inflammation and mesenchymal stem cell aging
title_sort inflammation and mesenchymal stem cell aging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167021/
https://www.ncbi.nlm.nih.gov/pubmed/21703839
http://dx.doi.org/10.1016/j.coi.2011.05.007
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