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pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice

Extracellular pH has the potential to affect various aspects of the pancreatic beta cell function. To explain this effect, a number of mechanisms was proposed involving both extracellular and intracellular targets and pathways. Here, we focus on reassessing the influence of extracellular pH on gluco...

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Autores principales: Postić, Sandra, Gosak, Marko, Tsai, Wen-Hao, Pfabe, Johannes, Sarikas, Srdjan, Stožer, Andraž, Korošak, Dean, Yang, Shi-Bing, Slak Rupnik, Marjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273738/
https://www.ncbi.nlm.nih.gov/pubmed/35837307
http://dx.doi.org/10.3389/fendo.2022.916688
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author Postić, Sandra
Gosak, Marko
Tsai, Wen-Hao
Pfabe, Johannes
Sarikas, Srdjan
Stožer, Andraž
Korošak, Dean
Yang, Shi-Bing
Slak Rupnik, Marjan
author_facet Postić, Sandra
Gosak, Marko
Tsai, Wen-Hao
Pfabe, Johannes
Sarikas, Srdjan
Stožer, Andraž
Korošak, Dean
Yang, Shi-Bing
Slak Rupnik, Marjan
author_sort Postić, Sandra
collection PubMed
description Extracellular pH has the potential to affect various aspects of the pancreatic beta cell function. To explain this effect, a number of mechanisms was proposed involving both extracellular and intracellular targets and pathways. Here, we focus on reassessing the influence of extracellular pH on glucose-dependent beta cell activation and collective activity in physiological conditions. To this end we employed mouse pancreatic tissue slices to perform high-temporally resolved functional imaging of cytosolic Ca(2+) oscillations. We investigated the effect of either physiological H(+) excess or depletion on the activation properties as well as on the collective activity of beta cell in an islet. Our results indicate that lowered pH invokes activation of a subset of beta cells in substimulatory glucose concentrations, enhances the average activity of beta cells, and alters the beta cell network properties in an islet. The enhanced average activity of beta cells was determined indirectly utilizing cytosolic Ca(2+) imaging, while direct measuring of insulin secretion confirmed that this enhanced activity is accompanied by a higher insulin release. Furthermore, reduced functional connectivity and higher functional segregation at lower pH, both signs of a reduced intercellular communication, do not necessary result in an impaired insulin release.
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spelling pubmed-92737382022-07-13 pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice Postić, Sandra Gosak, Marko Tsai, Wen-Hao Pfabe, Johannes Sarikas, Srdjan Stožer, Andraž Korošak, Dean Yang, Shi-Bing Slak Rupnik, Marjan Front Endocrinol (Lausanne) Endocrinology Extracellular pH has the potential to affect various aspects of the pancreatic beta cell function. To explain this effect, a number of mechanisms was proposed involving both extracellular and intracellular targets and pathways. Here, we focus on reassessing the influence of extracellular pH on glucose-dependent beta cell activation and collective activity in physiological conditions. To this end we employed mouse pancreatic tissue slices to perform high-temporally resolved functional imaging of cytosolic Ca(2+) oscillations. We investigated the effect of either physiological H(+) excess or depletion on the activation properties as well as on the collective activity of beta cell in an islet. Our results indicate that lowered pH invokes activation of a subset of beta cells in substimulatory glucose concentrations, enhances the average activity of beta cells, and alters the beta cell network properties in an islet. The enhanced average activity of beta cells was determined indirectly utilizing cytosolic Ca(2+) imaging, while direct measuring of insulin secretion confirmed that this enhanced activity is accompanied by a higher insulin release. Furthermore, reduced functional connectivity and higher functional segregation at lower pH, both signs of a reduced intercellular communication, do not necessary result in an impaired insulin release. Frontiers Media S.A. 2022-06-28 /pmc/articles/PMC9273738/ /pubmed/35837307 http://dx.doi.org/10.3389/fendo.2022.916688 Text en Copyright © 2022 Postić, Gosak, Tsai, Pfabe, Sarikas, Stožer, Korošak, Yang and Slak Rupnik https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Postić, Sandra
Gosak, Marko
Tsai, Wen-Hao
Pfabe, Johannes
Sarikas, Srdjan
Stožer, Andraž
Korošak, Dean
Yang, Shi-Bing
Slak Rupnik, Marjan
pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title_full pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title_fullStr pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title_full_unstemmed pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title_short pH-Dependence of Glucose-Dependent Activity of Beta Cell Networks in Acute Mouse Pancreatic Tissue Slice
title_sort ph-dependence of glucose-dependent activity of beta cell networks in acute mouse pancreatic tissue slice
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273738/
https://www.ncbi.nlm.nih.gov/pubmed/35837307
http://dx.doi.org/10.3389/fendo.2022.916688
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