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Glucocorticoid receptor action in metabolic and neuronal function

Glucocorticoids via the glucocorticoid receptor (GR) have effects on a variety of cell types, eliciting important physiological responses via changes in gene expression and signaling. Although decades of research have illuminated the mechanism of how this important steroid receptor controls gene exp...

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Autores principales: Garabedian, Michael J., Harris, Charles A., Jeanneteau, Freddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531160/
https://www.ncbi.nlm.nih.gov/pubmed/28781762
http://dx.doi.org/10.12688/f1000research.11375.1
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author Garabedian, Michael J.
Harris, Charles A.
Jeanneteau, Freddy
author_facet Garabedian, Michael J.
Harris, Charles A.
Jeanneteau, Freddy
author_sort Garabedian, Michael J.
collection PubMed
description Glucocorticoids via the glucocorticoid receptor (GR) have effects on a variety of cell types, eliciting important physiological responses via changes in gene expression and signaling. Although decades of research have illuminated the mechanism of how this important steroid receptor controls gene expression using in vitro and cell culture–based approaches, how GR responds to changes in external signals in vivo under normal and pathological conditions remains elusive. The goal of this review is to highlight recent work on GR action in fat cells and liver to affect metabolism in vivo and the role GR ligands and receptor phosphorylation play in calibrating signaling outputs by GR in the brain in health and disease. We also suggest that both the brain and fat tissue communicate to affect physiology and behavior and that understanding this “brain-fat axis” will enable a more complete understanding of metabolic diseases and inform new ways to target them.
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spelling pubmed-55311602017-08-04 Glucocorticoid receptor action in metabolic and neuronal function Garabedian, Michael J. Harris, Charles A. Jeanneteau, Freddy F1000Res Review Glucocorticoids via the glucocorticoid receptor (GR) have effects on a variety of cell types, eliciting important physiological responses via changes in gene expression and signaling. Although decades of research have illuminated the mechanism of how this important steroid receptor controls gene expression using in vitro and cell culture–based approaches, how GR responds to changes in external signals in vivo under normal and pathological conditions remains elusive. The goal of this review is to highlight recent work on GR action in fat cells and liver to affect metabolism in vivo and the role GR ligands and receptor phosphorylation play in calibrating signaling outputs by GR in the brain in health and disease. We also suggest that both the brain and fat tissue communicate to affect physiology and behavior and that understanding this “brain-fat axis” will enable a more complete understanding of metabolic diseases and inform new ways to target them. F1000Research 2017-07-24 /pmc/articles/PMC5531160/ /pubmed/28781762 http://dx.doi.org/10.12688/f1000research.11375.1 Text en Copyright: © 2017 Garabedian MJ et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Garabedian, Michael J.
Harris, Charles A.
Jeanneteau, Freddy
Glucocorticoid receptor action in metabolic and neuronal function
title Glucocorticoid receptor action in metabolic and neuronal function
title_full Glucocorticoid receptor action in metabolic and neuronal function
title_fullStr Glucocorticoid receptor action in metabolic and neuronal function
title_full_unstemmed Glucocorticoid receptor action in metabolic and neuronal function
title_short Glucocorticoid receptor action in metabolic and neuronal function
title_sort glucocorticoid receptor action in metabolic and neuronal function
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531160/
https://www.ncbi.nlm.nih.gov/pubmed/28781762
http://dx.doi.org/10.12688/f1000research.11375.1
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