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Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells

Objective: Investigate the involvement of the fatty acids receptor GPR40 in the assembly and activation of NADPH oxidase and the implications on pancreatic β-cell function. Methods: BRIN-BD11 β-cells were exposed to GPR40 agonist (GW9508) or linoleic acid in different glucose concentrations. Superox...

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Autores principales: Nunes Marsiglio-Librais, Gabriela, Aparecida Vilas-Boas, Eloisa, Carlein, Christopher, Hoffmann, Markus Daniel Alexander, Roma, Leticia Prates, Carpinelli, Angelo Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241480/
https://www.ncbi.nlm.nih.gov/pubmed/32354273
http://dx.doi.org/10.1080/13510002.2020.1757877
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author Nunes Marsiglio-Librais, Gabriela
Aparecida Vilas-Boas, Eloisa
Carlein, Christopher
Hoffmann, Markus Daniel Alexander
Roma, Leticia Prates
Carpinelli, Angelo Rafael
author_facet Nunes Marsiglio-Librais, Gabriela
Aparecida Vilas-Boas, Eloisa
Carlein, Christopher
Hoffmann, Markus Daniel Alexander
Roma, Leticia Prates
Carpinelli, Angelo Rafael
author_sort Nunes Marsiglio-Librais, Gabriela
collection PubMed
description Objective: Investigate the involvement of the fatty acids receptor GPR40 in the assembly and activation of NADPH oxidase and the implications on pancreatic β-cell function. Methods: BRIN-BD11 β-cells were exposed to GPR40 agonist (GW9508) or linoleic acid in different glucose concentrations. Superoxide and H(2)O(2) were analyzed, respectively, by DHE fluorescence and by fluorescence of the H(2)O(2) sensor, roGFP2-Orp1. Protein contents of p47(phox) in plasma membrane and cytosol were analyzed by western blot. NADPH oxidase role was evaluated by p22(phox) siRNA or by pharmacological inhibition with VAS2870. NOX2 KO islets were used to measure total cytosolic calcium and insulin secretion. Results: GW9508 and linoleic acid increased superoxide and H(2)O(2) contents at 5.6 and 8.3 mM of glucose. In addition, in 5.6 mM, but not at 16.7 mM of glucose, activation of GPR40 led to the translocation of p47(phox) to the plasma membrane. Knockdown of p22(phox) abolished the increase in superoxide after GW9508 and linoleic acid. No differences in insulin secretion were found between wild type and NOX2 KO islets treated with GW9508 or linoleic acid. Discussion: We report for the first time that acute activation of GPR40 leads to NADPH oxidase activation in pancreatic β-cells, without impact on insulin secretion.
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spelling pubmed-72414802020-06-01 Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells Nunes Marsiglio-Librais, Gabriela Aparecida Vilas-Boas, Eloisa Carlein, Christopher Hoffmann, Markus Daniel Alexander Roma, Leticia Prates Carpinelli, Angelo Rafael Redox Rep Research Articles Objective: Investigate the involvement of the fatty acids receptor GPR40 in the assembly and activation of NADPH oxidase and the implications on pancreatic β-cell function. Methods: BRIN-BD11 β-cells were exposed to GPR40 agonist (GW9508) or linoleic acid in different glucose concentrations. Superoxide and H(2)O(2) were analyzed, respectively, by DHE fluorescence and by fluorescence of the H(2)O(2) sensor, roGFP2-Orp1. Protein contents of p47(phox) in plasma membrane and cytosol were analyzed by western blot. NADPH oxidase role was evaluated by p22(phox) siRNA or by pharmacological inhibition with VAS2870. NOX2 KO islets were used to measure total cytosolic calcium and insulin secretion. Results: GW9508 and linoleic acid increased superoxide and H(2)O(2) contents at 5.6 and 8.3 mM of glucose. In addition, in 5.6 mM, but not at 16.7 mM of glucose, activation of GPR40 led to the translocation of p47(phox) to the plasma membrane. Knockdown of p22(phox) abolished the increase in superoxide after GW9508 and linoleic acid. No differences in insulin secretion were found between wild type and NOX2 KO islets treated with GW9508 or linoleic acid. Discussion: We report for the first time that acute activation of GPR40 leads to NADPH oxidase activation in pancreatic β-cells, without impact on insulin secretion. Taylor & Francis 2020-05-01 /pmc/articles/PMC7241480/ /pubmed/32354273 http://dx.doi.org/10.1080/13510002.2020.1757877 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Nunes Marsiglio-Librais, Gabriela
Aparecida Vilas-Boas, Eloisa
Carlein, Christopher
Hoffmann, Markus Daniel Alexander
Roma, Leticia Prates
Carpinelli, Angelo Rafael
Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title_full Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title_fullStr Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title_full_unstemmed Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title_short Evidence for NADPH oxidase activation by GPR40 in pancreatic β-cells
title_sort evidence for nadph oxidase activation by gpr40 in pancreatic β-cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241480/
https://www.ncbi.nlm.nih.gov/pubmed/32354273
http://dx.doi.org/10.1080/13510002.2020.1757877
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