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Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice

White adipose tissue (WAT) is distributed in several depots with distinct metabolic and inflammatory functions. In our body there are subcutaneous (sWAT), visceral (vWAT) and bone marrow (bWAT) fat depots. Obesity affects the size, function and inflammatory state of WATs. In particular, obesity may...

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Autores principales: Alessio, Nicola, Acar, Mustafa B., Demirsoy, Ibrahim H., Squillaro, Tiziana, Siniscalco, Dario, Bernardo, Giovanni Di, Peluso, Gianfranco, Özcan, Servet, Galderisi, Umberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377882/
https://www.ncbi.nlm.nih.gov/pubmed/32634118
http://dx.doi.org/10.18632/aging.103606
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author Alessio, Nicola
Acar, Mustafa B.
Demirsoy, Ibrahim H.
Squillaro, Tiziana
Siniscalco, Dario
Bernardo, Giovanni Di
Peluso, Gianfranco
Özcan, Servet
Galderisi, Umberto
author_facet Alessio, Nicola
Acar, Mustafa B.
Demirsoy, Ibrahim H.
Squillaro, Tiziana
Siniscalco, Dario
Bernardo, Giovanni Di
Peluso, Gianfranco
Özcan, Servet
Galderisi, Umberto
author_sort Alessio, Nicola
collection PubMed
description White adipose tissue (WAT) is distributed in several depots with distinct metabolic and inflammatory functions. In our body there are subcutaneous (sWAT), visceral (vWAT) and bone marrow (bWAT) fat depots. Obesity affects the size, function and inflammatory state of WATs. In particular, obesity may affect the activity of mesenchymal stromal cells (MSCs) present in WAT. MSCs are a heterogeneous population containing stromal cells, progenitor cells, fibroblasts and stem cells that are able to differentiate among adipocytes, chondrocytes, osteocytes and other mesodermal derivatives. In the first study of this kind, we performed a comparison of the effects of obesity on MSCs obtained from sWAT, vWAT and bWAT. Our study showed that obesity affects mainly the biological functions of MSCs obtained from bone marrow and vWAT by decreasing the proliferation rate, reducing the percentage of cells in S phase and triggering senescence. The onset of senescence was confirmed by expression of genes belonging to RB and P53 pathways. Our study revealed that the negative consequences of obesity on body physiology may also be related to impairment in the functions of the stromal compartment present in the several adipose tissues. This finding provides new insights as to the targets that should be considered for an effective treatment of obesity-related diseases.
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spelling pubmed-73778822020-07-31 Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice Alessio, Nicola Acar, Mustafa B. Demirsoy, Ibrahim H. Squillaro, Tiziana Siniscalco, Dario Bernardo, Giovanni Di Peluso, Gianfranco Özcan, Servet Galderisi, Umberto Aging (Albany NY) Research Paper White adipose tissue (WAT) is distributed in several depots with distinct metabolic and inflammatory functions. In our body there are subcutaneous (sWAT), visceral (vWAT) and bone marrow (bWAT) fat depots. Obesity affects the size, function and inflammatory state of WATs. In particular, obesity may affect the activity of mesenchymal stromal cells (MSCs) present in WAT. MSCs are a heterogeneous population containing stromal cells, progenitor cells, fibroblasts and stem cells that are able to differentiate among adipocytes, chondrocytes, osteocytes and other mesodermal derivatives. In the first study of this kind, we performed a comparison of the effects of obesity on MSCs obtained from sWAT, vWAT and bWAT. Our study showed that obesity affects mainly the biological functions of MSCs obtained from bone marrow and vWAT by decreasing the proliferation rate, reducing the percentage of cells in S phase and triggering senescence. The onset of senescence was confirmed by expression of genes belonging to RB and P53 pathways. Our study revealed that the negative consequences of obesity on body physiology may also be related to impairment in the functions of the stromal compartment present in the several adipose tissues. This finding provides new insights as to the targets that should be considered for an effective treatment of obesity-related diseases. Impact Journals 2020-07-07 /pmc/articles/PMC7377882/ /pubmed/32634118 http://dx.doi.org/10.18632/aging.103606 Text en Copyright © 2020 Alessio et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Alessio, Nicola
Acar, Mustafa B.
Demirsoy, Ibrahim H.
Squillaro, Tiziana
Siniscalco, Dario
Bernardo, Giovanni Di
Peluso, Gianfranco
Özcan, Servet
Galderisi, Umberto
Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title_full Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title_fullStr Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title_full_unstemmed Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title_short Obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
title_sort obesity is associated with senescence of mesenchymal stromal cells derived from bone marrow, subcutaneous and visceral fat of young mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377882/
https://www.ncbi.nlm.nih.gov/pubmed/32634118
http://dx.doi.org/10.18632/aging.103606
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