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Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice

Bariatric surgery improves both insulin sensitivity and secretion and can induce diabetes remission. However, the mechanisms and time courses of these changes, particularly the impact on β cell function, are difficult to monitor directly. In this study, we investigated the effect of Vertical Sleeve...

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Autores principales: Akalestou, Elina, Suba, Kinga, Lopez-Noriega, Livia, Georgiadou, Eleni, Chabosseau, Pauline, Gallie, Alasdair, Wretlind, Asger, Legido-Quigley, Cristina, Leclerc, Isabelle, Salem, Victoria, Rutter, Guy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397709/
https://www.ncbi.nlm.nih.gov/pubmed/34453049
http://dx.doi.org/10.1038/s41467-021-25423-8
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author Akalestou, Elina
Suba, Kinga
Lopez-Noriega, Livia
Georgiadou, Eleni
Chabosseau, Pauline
Gallie, Alasdair
Wretlind, Asger
Legido-Quigley, Cristina
Leclerc, Isabelle
Salem, Victoria
Rutter, Guy A.
author_facet Akalestou, Elina
Suba, Kinga
Lopez-Noriega, Livia
Georgiadou, Eleni
Chabosseau, Pauline
Gallie, Alasdair
Wretlind, Asger
Legido-Quigley, Cristina
Leclerc, Isabelle
Salem, Victoria
Rutter, Guy A.
author_sort Akalestou, Elina
collection PubMed
description Bariatric surgery improves both insulin sensitivity and secretion and can induce diabetes remission. However, the mechanisms and time courses of these changes, particularly the impact on β cell function, are difficult to monitor directly. In this study, we investigated the effect of Vertical Sleeve Gastrectomy (VSG) on β cell function in vivo by imaging Ca(2+) dynamics in islets engrafted into the anterior eye chamber. Mirroring its clinical utility, VSG in mice results in significantly improved glucose tolerance, and enhanced insulin secretion. We reveal that these benefits are underpinned by augmented β cell function and coordinated activity across the islet. These effects involve changes in circulating GLP-1 levels which may act both directly and indirectly on the β cell, in the latter case through changes in body weight. Thus, bariatric surgery leads to time-dependent increases in β cell function and intra-islet connectivity which are likely to contribute to diabetes remission.
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spelling pubmed-83977092021-10-07 Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice Akalestou, Elina Suba, Kinga Lopez-Noriega, Livia Georgiadou, Eleni Chabosseau, Pauline Gallie, Alasdair Wretlind, Asger Legido-Quigley, Cristina Leclerc, Isabelle Salem, Victoria Rutter, Guy A. Nat Commun Article Bariatric surgery improves both insulin sensitivity and secretion and can induce diabetes remission. However, the mechanisms and time courses of these changes, particularly the impact on β cell function, are difficult to monitor directly. In this study, we investigated the effect of Vertical Sleeve Gastrectomy (VSG) on β cell function in vivo by imaging Ca(2+) dynamics in islets engrafted into the anterior eye chamber. Mirroring its clinical utility, VSG in mice results in significantly improved glucose tolerance, and enhanced insulin secretion. We reveal that these benefits are underpinned by augmented β cell function and coordinated activity across the islet. These effects involve changes in circulating GLP-1 levels which may act both directly and indirectly on the β cell, in the latter case through changes in body weight. Thus, bariatric surgery leads to time-dependent increases in β cell function and intra-islet connectivity which are likely to contribute to diabetes remission. Nature Publishing Group UK 2021-08-27 /pmc/articles/PMC8397709/ /pubmed/34453049 http://dx.doi.org/10.1038/s41467-021-25423-8 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Akalestou, Elina
Suba, Kinga
Lopez-Noriega, Livia
Georgiadou, Eleni
Chabosseau, Pauline
Gallie, Alasdair
Wretlind, Asger
Legido-Quigley, Cristina
Leclerc, Isabelle
Salem, Victoria
Rutter, Guy A.
Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title_full Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title_fullStr Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title_full_unstemmed Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title_short Intravital imaging of islet Ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
title_sort intravital imaging of islet ca(2+) dynamics reveals enhanced β cell connectivity after bariatric surgery in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397709/
https://www.ncbi.nlm.nih.gov/pubmed/34453049
http://dx.doi.org/10.1038/s41467-021-25423-8
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