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MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects

We investigated miR21 expression in omental (OAT) and subcutaneous adipose tissue (SAT) from 16 obese subjects undergoing bariatric surgery. Patients were divided into two age- and BMI-matched groups according to the presence of type 2 diabetes (T2D). miR21 was not differently expressed in OAT and S...

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Autores principales: Guglielmi, Valeria, D’Adamo, Monica, Menghini, Rossella, Cardellini, Marina, Gentileschi, Paolo, Federici, Massimo, Sbraccia, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389040/
https://www.ncbi.nlm.nih.gov/pubmed/28447068
http://dx.doi.org/10.3233/NHA-160020
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author Guglielmi, Valeria
D’Adamo, Monica
Menghini, Rossella
Cardellini, Marina
Gentileschi, Paolo
Federici, Massimo
Sbraccia, Paolo
author_facet Guglielmi, Valeria
D’Adamo, Monica
Menghini, Rossella
Cardellini, Marina
Gentileschi, Paolo
Federici, Massimo
Sbraccia, Paolo
author_sort Guglielmi, Valeria
collection PubMed
description We investigated miR21 expression in omental (OAT) and subcutaneous adipose tissue (SAT) from 16 obese subjects undergoing bariatric surgery. Patients were divided into two age- and BMI-matched groups according to the presence of type 2 diabetes (T2D). miR21 was not differently expressed in OAT and SAT. However, miR21 expression was two folds greater in adipose tissue in patients with T2D. Accordingly, in primary cultures of adipocytes from non diabetic overweight subjects, miR21 expression increased after 24-h exposure to high glucose and insulin. In conclusion, miR21 appears linked to insulin-resistance deterioration within its pathophysiologic progression from obesity to T2D.
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spelling pubmed-53890402017-04-24 MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects Guglielmi, Valeria D’Adamo, Monica Menghini, Rossella Cardellini, Marina Gentileschi, Paolo Federici, Massimo Sbraccia, Paolo Nutr Healthy Aging Brief Communication We investigated miR21 expression in omental (OAT) and subcutaneous adipose tissue (SAT) from 16 obese subjects undergoing bariatric surgery. Patients were divided into two age- and BMI-matched groups according to the presence of type 2 diabetes (T2D). miR21 was not differently expressed in OAT and SAT. However, miR21 expression was two folds greater in adipose tissue in patients with T2D. Accordingly, in primary cultures of adipocytes from non diabetic overweight subjects, miR21 expression increased after 24-h exposure to high glucose and insulin. In conclusion, miR21 appears linked to insulin-resistance deterioration within its pathophysiologic progression from obesity to T2D. IOS Press 2017-03-31 /pmc/articles/PMC5389040/ /pubmed/28447068 http://dx.doi.org/10.3233/NHA-160020 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Guglielmi, Valeria
D’Adamo, Monica
Menghini, Rossella
Cardellini, Marina
Gentileschi, Paolo
Federici, Massimo
Sbraccia, Paolo
MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title_full MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title_fullStr MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title_full_unstemmed MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title_short MicroRNA 21 is up-regulated in adipose tissue of obese diabetic subjects
title_sort microrna 21 is up-regulated in adipose tissue of obese diabetic subjects
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389040/
https://www.ncbi.nlm.nih.gov/pubmed/28447068
http://dx.doi.org/10.3233/NHA-160020
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