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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8397709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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