20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1

FFAR1 receptor is highly expressed in beta cells and its activation has been suggested as therapy against type-2 diabetes. Here, Tunaru et al. show that 20-hydroxyeicosatetraenoic acid, produced within the islets upon glucose stimulation, acts in an autocrine manner to stimulate insulin secretion vi...

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Autores principales: Sorin Tunaru, Remy Bonnavion, Isabell Brandenburger, Jens Preussner, Dominique Thomas, Klaus Scholich, Stefan Offermanns
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/9a7ee26cbe794bc5b4667eb9d97b5e93
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spelling oai:doaj.org-article:9a7ee26cbe794bc5b4667eb9d97b5e932021-12-02T17:32:02Z20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR110.1038/s41467-017-02539-42041-1723https://doaj.org/article/9a7ee26cbe794bc5b4667eb9d97b5e932018-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-02539-4https://doaj.org/toc/2041-1723FFAR1 receptor is highly expressed in beta cells and its activation has been suggested as therapy against type-2 diabetes. Here, Tunaru et al. show that 20-hydroxyeicosatetraenoic acid, produced within the islets upon glucose stimulation, acts in an autocrine manner to stimulate insulin secretion via FFAR1 activation.Sorin TunaruRemy BonnavionIsabell BrandenburgerJens PreussnerDominique ThomasKlaus ScholichStefan OffermannsNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Sorin Tunaru
Remy Bonnavion
Isabell Brandenburger
Jens Preussner
Dominique Thomas
Klaus Scholich
Stefan Offermanns
20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
description FFAR1 receptor is highly expressed in beta cells and its activation has been suggested as therapy against type-2 diabetes. Here, Tunaru et al. show that 20-hydroxyeicosatetraenoic acid, produced within the islets upon glucose stimulation, acts in an autocrine manner to stimulate insulin secretion via FFAR1 activation.
format article
author Sorin Tunaru
Remy Bonnavion
Isabell Brandenburger
Jens Preussner
Dominique Thomas
Klaus Scholich
Stefan Offermanns
author_facet Sorin Tunaru
Remy Bonnavion
Isabell Brandenburger
Jens Preussner
Dominique Thomas
Klaus Scholich
Stefan Offermanns
author_sort Sorin Tunaru
title 20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
title_short 20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
title_full 20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
title_fullStr 20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
title_full_unstemmed 20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
title_sort 20-hete promotes glucose-stimulated insulin secretion in an autocrine manner through ffar1
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/9a7ee26cbe794bc5b4667eb9d97b5e93
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AT isabellbrandenburger 20hetepromotesglucosestimulatedinsulinsecretioninanautocrinemannerthroughffar1
AT jenspreussner 20hetepromotesglucosestimulatedinsulinsecretioninanautocrinemannerthroughffar1
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