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Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging
Mesenchymal stem/stromal cells (MSCs) are a reservoir for tissue homeostasis and repair that age during organismal aging. Beside the fundamental in vivo role of MSCs, they have also emerged in the last years as extremely promising therapeutic agents for a wide variety of clinical conditions. MSC use...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072652/ https://www.ncbi.nlm.nih.gov/pubmed/32098040 http://dx.doi.org/10.3390/biom10020340 |
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author | Neri, Simona Borzì, Rosa Maria |
author_facet | Neri, Simona Borzì, Rosa Maria |
author_sort | Neri, Simona |
collection | PubMed |
description | Mesenchymal stem/stromal cells (MSCs) are a reservoir for tissue homeostasis and repair that age during organismal aging. Beside the fundamental in vivo role of MSCs, they have also emerged in the last years as extremely promising therapeutic agents for a wide variety of clinical conditions. MSC use frequently requires in vitro expansion, thus exposing cells to replicative senescence. Aging of MSCs (both in vivo and in vitro) can affect not only their replicative potential, but also their properties, like immunomodulation and secretory profile, thus possibly compromising their therapeutic effect. It is therefore of critical importance to unveil the underlying mechanisms of MSC senescence and to define shared methods to assess MSC aging status. The present review will focus on current scientific knowledge about MSC aging mechanisms, control and effects, including possible anti-aging treatments. |
format | Online Article Text |
id | pubmed-7072652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70726522020-03-19 Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging Neri, Simona Borzì, Rosa Maria Biomolecules Review Mesenchymal stem/stromal cells (MSCs) are a reservoir for tissue homeostasis and repair that age during organismal aging. Beside the fundamental in vivo role of MSCs, they have also emerged in the last years as extremely promising therapeutic agents for a wide variety of clinical conditions. MSC use frequently requires in vitro expansion, thus exposing cells to replicative senescence. Aging of MSCs (both in vivo and in vitro) can affect not only their replicative potential, but also their properties, like immunomodulation and secretory profile, thus possibly compromising their therapeutic effect. It is therefore of critical importance to unveil the underlying mechanisms of MSC senescence and to define shared methods to assess MSC aging status. The present review will focus on current scientific knowledge about MSC aging mechanisms, control and effects, including possible anti-aging treatments. MDPI 2020-02-21 /pmc/articles/PMC7072652/ /pubmed/32098040 http://dx.doi.org/10.3390/biom10020340 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Neri, Simona Borzì, Rosa Maria Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title | Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title_full | Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title_fullStr | Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title_full_unstemmed | Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title_short | Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging |
title_sort | molecular mechanisms contributing to mesenchymal stromal cell aging |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072652/ https://www.ncbi.nlm.nih.gov/pubmed/32098040 http://dx.doi.org/10.3390/biom10020340 |
work_keys_str_mv | AT nerisimona molecularmechanismscontributingtomesenchymalstromalcellaging AT borzirosamaria molecularmechanismscontributingtomesenchymalstromalcellaging |