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GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation

Glucagon-like peptide-1 (GLP-1) promotes insulin secretion from pancreatic β-cells in a glucose dependent manner. Several pathways mediate this action by rapid, kinase phosphorylation-dependent, but gene expression-independent mechanisms. Since GLP-1-induced insulin secretion requires glucose metabo...

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Autores principales: Carlessi, Rodrigo, Chen, Younan, Rowlands, Jordan, Cruzat, Vinicius F., Keane, Kevin N., Egan, Lauren, Mamotte, Cyril, Stokes, Rebecca, Gunton, Jenny E., Bittencourt, Paulo Ivo Homem de, Newsholme, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454020/
https://www.ncbi.nlm.nih.gov/pubmed/28572610
http://dx.doi.org/10.1038/s41598-017-02838-2
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author Carlessi, Rodrigo
Chen, Younan
Rowlands, Jordan
Cruzat, Vinicius F.
Keane, Kevin N.
Egan, Lauren
Mamotte, Cyril
Stokes, Rebecca
Gunton, Jenny E.
Bittencourt, Paulo Ivo Homem de
Newsholme, Philip
author_facet Carlessi, Rodrigo
Chen, Younan
Rowlands, Jordan
Cruzat, Vinicius F.
Keane, Kevin N.
Egan, Lauren
Mamotte, Cyril
Stokes, Rebecca
Gunton, Jenny E.
Bittencourt, Paulo Ivo Homem de
Newsholme, Philip
author_sort Carlessi, Rodrigo
collection PubMed
description Glucagon-like peptide-1 (GLP-1) promotes insulin secretion from pancreatic β-cells in a glucose dependent manner. Several pathways mediate this action by rapid, kinase phosphorylation-dependent, but gene expression-independent mechanisms. Since GLP-1-induced insulin secretion requires glucose metabolism, we aimed to address the hypothesis that GLP-1 receptor (GLP-1R) signalling can modulate glucose uptake and utilization in β-cells. We have assessed various metabolic parameters after short and long exposure of clonal BRIN-BD11 β-cells and rodent islets to the GLP-1R agonist Exendin-4 (50 nM). Here we report for the first time that prolonged stimulation of the GLP-1R for 18 hours promotes metabolic reprogramming of β-cells. This is evidenced by up-regulation of glycolytic enzyme expression, increased rates of glucose uptake and consumption, as well as augmented ATP content, insulin secretion and glycolytic flux after removal of Exendin-4. In our model, depletion of Hypoxia-Inducible Factor 1 alpha (HIF-1α) impaired the effects of Exendin-4 on glucose metabolism, while pharmacological inhibition of Phosphoinositide 3-kinase (PI3K) or mTOR completely abolished such effects. Considering the central role of glucose catabolism for stimulus-secretion coupling in β-cells, our findings suggest that chronic GLP-1 actions on insulin secretion include elevated β-cell glucose metabolism. Moreover, our data reveal novel aspects of GLP-1 stimulated insulin secretion involving de novo gene expression.
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spelling pubmed-54540202017-06-06 GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation Carlessi, Rodrigo Chen, Younan Rowlands, Jordan Cruzat, Vinicius F. Keane, Kevin N. Egan, Lauren Mamotte, Cyril Stokes, Rebecca Gunton, Jenny E. Bittencourt, Paulo Ivo Homem de Newsholme, Philip Sci Rep Article Glucagon-like peptide-1 (GLP-1) promotes insulin secretion from pancreatic β-cells in a glucose dependent manner. Several pathways mediate this action by rapid, kinase phosphorylation-dependent, but gene expression-independent mechanisms. Since GLP-1-induced insulin secretion requires glucose metabolism, we aimed to address the hypothesis that GLP-1 receptor (GLP-1R) signalling can modulate glucose uptake and utilization in β-cells. We have assessed various metabolic parameters after short and long exposure of clonal BRIN-BD11 β-cells and rodent islets to the GLP-1R agonist Exendin-4 (50 nM). Here we report for the first time that prolonged stimulation of the GLP-1R for 18 hours promotes metabolic reprogramming of β-cells. This is evidenced by up-regulation of glycolytic enzyme expression, increased rates of glucose uptake and consumption, as well as augmented ATP content, insulin secretion and glycolytic flux after removal of Exendin-4. In our model, depletion of Hypoxia-Inducible Factor 1 alpha (HIF-1α) impaired the effects of Exendin-4 on glucose metabolism, while pharmacological inhibition of Phosphoinositide 3-kinase (PI3K) or mTOR completely abolished such effects. Considering the central role of glucose catabolism for stimulus-secretion coupling in β-cells, our findings suggest that chronic GLP-1 actions on insulin secretion include elevated β-cell glucose metabolism. Moreover, our data reveal novel aspects of GLP-1 stimulated insulin secretion involving de novo gene expression. Nature Publishing Group UK 2017-06-01 /pmc/articles/PMC5454020/ /pubmed/28572610 http://dx.doi.org/10.1038/s41598-017-02838-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Carlessi, Rodrigo
Chen, Younan
Rowlands, Jordan
Cruzat, Vinicius F.
Keane, Kevin N.
Egan, Lauren
Mamotte, Cyril
Stokes, Rebecca
Gunton, Jenny E.
Bittencourt, Paulo Ivo Homem de
Newsholme, Philip
GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title_full GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title_fullStr GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title_full_unstemmed GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title_short GLP-1 receptor signalling promotes β-cell glucose metabolism via mTOR-dependent HIF-1α activation
title_sort glp-1 receptor signalling promotes β-cell glucose metabolism via mtor-dependent hif-1α activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454020/
https://www.ncbi.nlm.nih.gov/pubmed/28572610
http://dx.doi.org/10.1038/s41598-017-02838-2
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