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Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5

Adipose tissue is a significant source of mesenchymal stem cells for regenerative therapies; however, caution should be taken as their environmental niche can affect their functional properties. We have previously demonstrated the negative impact of obesity on the function of adipose-derived stem ce...

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Detalles Bibliográficos
Autores principales: Pérez, Laura M., de Lucas, Beatriz, Lunyak, Victoria V., Gálvez, Beatriz G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447652/
https://www.ncbi.nlm.nih.gov/pubmed/28580301
http://dx.doi.org/10.1016/j.ymgmr.2017.05.008
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author Pérez, Laura M.
de Lucas, Beatriz
Lunyak, Victoria V.
Gálvez, Beatriz G.
author_facet Pérez, Laura M.
de Lucas, Beatriz
Lunyak, Victoria V.
Gálvez, Beatriz G.
author_sort Pérez, Laura M.
collection PubMed
description Adipose tissue is a significant source of mesenchymal stem cells for regenerative therapies; however, caution should be taken as their environmental niche can affect their functional properties. We have previously demonstrated the negative impact of obesity on the function of adipose-derived stem cells (ASCs). Here we have evaluated other possible properties and targets that are altered by obesity such as the recently described long non-coding molecule Gas5, which is involved in glucocorticoid resistance. Using ASCs isolated from obese (oASCs) and control subjects (cASCs), we have analyzed additional metabolic and inflammatory conditions that could be related with their impaired therapeutic potential and consequently their possible usefulness in the clinic.
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spelling pubmed-54476522017-06-02 Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5 Pérez, Laura M. de Lucas, Beatriz Lunyak, Victoria V. Gálvez, Beatriz G. Mol Genet Metab Rep Short Communication Adipose tissue is a significant source of mesenchymal stem cells for regenerative therapies; however, caution should be taken as their environmental niche can affect their functional properties. We have previously demonstrated the negative impact of obesity on the function of adipose-derived stem cells (ASCs). Here we have evaluated other possible properties and targets that are altered by obesity such as the recently described long non-coding molecule Gas5, which is involved in glucocorticoid resistance. Using ASCs isolated from obese (oASCs) and control subjects (cASCs), we have analyzed additional metabolic and inflammatory conditions that could be related with their impaired therapeutic potential and consequently their possible usefulness in the clinic. Elsevier 2017-05-27 /pmc/articles/PMC5447652/ /pubmed/28580301 http://dx.doi.org/10.1016/j.ymgmr.2017.05.008 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Pérez, Laura M.
de Lucas, Beatriz
Lunyak, Victoria V.
Gálvez, Beatriz G.
Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title_full Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title_fullStr Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title_full_unstemmed Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title_short Adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin D and Gas5
title_sort adipose stem cells from obese patients show specific differences in the metabolic regulators vitamin d and gas5
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447652/
https://www.ncbi.nlm.nih.gov/pubmed/28580301
http://dx.doi.org/10.1016/j.ymgmr.2017.05.008
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