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Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling
Presence of thermogenically active adipose tissue in adult humans has been inversely associated with obesity and type 2 diabetes. While it had been shown that insulin is crucial for the development of classical brown fat, its role in development and function of inducible brown-in-white (brite) adipo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197027/ https://www.ncbi.nlm.nih.gov/pubmed/25313899 http://dx.doi.org/10.1371/journal.pone.0110428 |
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author | Mössenböck, Karin Vegiopoulos, Alexandros Rose, Adam J. Sijmonsma, Tjeerd P. Herzig, Stephan Schafmeier, Tobias |
author_facet | Mössenböck, Karin Vegiopoulos, Alexandros Rose, Adam J. Sijmonsma, Tjeerd P. Herzig, Stephan Schafmeier, Tobias |
author_sort | Mössenböck, Karin |
collection | PubMed |
description | Presence of thermogenically active adipose tissue in adult humans has been inversely associated with obesity and type 2 diabetes. While it had been shown that insulin is crucial for the development of classical brown fat, its role in development and function of inducible brown-in-white (brite) adipose tissue is less clear. Here we show that insulin deficiency impaired differentiation of brite adipocytes. However, adrenergic stimulation almost fully induced the thermogenic program under these settings. Although brite differentiation of adipocytes as well as browning of white adipose tissue entailed substantially elevated glucose uptake by adipose tissue, the capacity of insulin to stimulate glucose uptake surprisingly was not higher in the brite state. Notably, in line with the insulin-independent stimulation of glucose uptake, our data revealed that brite recruitment results in induction of solute carrier family 2 (GLUT-1) expression in adipocytes and inguinal WAT. These results for the first time demonstrate that insulin signaling is neither essential for brite recruitment, nor is it improved in cells or tissues upon browning. |
format | Online Article Text |
id | pubmed-4197027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41970272014-10-16 Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling Mössenböck, Karin Vegiopoulos, Alexandros Rose, Adam J. Sijmonsma, Tjeerd P. Herzig, Stephan Schafmeier, Tobias PLoS One Research Article Presence of thermogenically active adipose tissue in adult humans has been inversely associated with obesity and type 2 diabetes. While it had been shown that insulin is crucial for the development of classical brown fat, its role in development and function of inducible brown-in-white (brite) adipose tissue is less clear. Here we show that insulin deficiency impaired differentiation of brite adipocytes. However, adrenergic stimulation almost fully induced the thermogenic program under these settings. Although brite differentiation of adipocytes as well as browning of white adipose tissue entailed substantially elevated glucose uptake by adipose tissue, the capacity of insulin to stimulate glucose uptake surprisingly was not higher in the brite state. Notably, in line with the insulin-independent stimulation of glucose uptake, our data revealed that brite recruitment results in induction of solute carrier family 2 (GLUT-1) expression in adipocytes and inguinal WAT. These results for the first time demonstrate that insulin signaling is neither essential for brite recruitment, nor is it improved in cells or tissues upon browning. Public Library of Science 2014-10-14 /pmc/articles/PMC4197027/ /pubmed/25313899 http://dx.doi.org/10.1371/journal.pone.0110428 Text en © 2014 Mössenböck et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mössenböck, Karin Vegiopoulos, Alexandros Rose, Adam J. Sijmonsma, Tjeerd P. Herzig, Stephan Schafmeier, Tobias Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title | Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title_full | Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title_fullStr | Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title_full_unstemmed | Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title_short | Browning of White Adipose Tissue Uncouples Glucose Uptake from Insulin Signaling |
title_sort | browning of white adipose tissue uncouples glucose uptake from insulin signaling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197027/ https://www.ncbi.nlm.nih.gov/pubmed/25313899 http://dx.doi.org/10.1371/journal.pone.0110428 |
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