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Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ
Cholinergic innervation in the pancreas controls both the release of digestive enzymes to support the intestinal digestion and absorption, as well as insulin release to promote nutrient use in the cells of the body. The effects of muscarinic receptor stimulation are described in detail for endocrine...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305080/ https://www.ncbi.nlm.nih.gov/pubmed/34201461 http://dx.doi.org/10.3390/cells10071580 |
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author | Sluga, Nastja Postić, Sandra Sarikas, Srdjan Huang, Ya-Chi Stožer, Andraž Slak Rupnik, Marjan |
author_facet | Sluga, Nastja Postić, Sandra Sarikas, Srdjan Huang, Ya-Chi Stožer, Andraž Slak Rupnik, Marjan |
author_sort | Sluga, Nastja |
collection | PubMed |
description | Cholinergic innervation in the pancreas controls both the release of digestive enzymes to support the intestinal digestion and absorption, as well as insulin release to promote nutrient use in the cells of the body. The effects of muscarinic receptor stimulation are described in detail for endocrine beta cells and exocrine acinar cells separately. Here we describe morphological and functional criteria to separate these two cell types in situ in tissue slices and simultaneously measure their response to ACh stimulation on cytosolic Ca(2+) oscillations [Ca(2+)](c) in stimulatory glucose conditions. Our results show that both cell types respond to glucose directly in the concentration range compatible with the glucose transporters they express. The physiological ACh concentration increases the frequency of glucose stimulated [Ca(2+)](c) oscillations in both cell types and synchronizes [Ca(2+)](c) oscillations in acinar cells. The supraphysiological ACh concentration further increases the oscillation frequency on the level of individual beta cells, inhibits the synchronization between these cells, and abolishes oscillatory activity in acinar cells. We discuss possible mechanisms leading to the observed phenomena. |
format | Online Article Text |
id | pubmed-8305080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83050802021-07-25 Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ Sluga, Nastja Postić, Sandra Sarikas, Srdjan Huang, Ya-Chi Stožer, Andraž Slak Rupnik, Marjan Cells Article Cholinergic innervation in the pancreas controls both the release of digestive enzymes to support the intestinal digestion and absorption, as well as insulin release to promote nutrient use in the cells of the body. The effects of muscarinic receptor stimulation are described in detail for endocrine beta cells and exocrine acinar cells separately. Here we describe morphological and functional criteria to separate these two cell types in situ in tissue slices and simultaneously measure their response to ACh stimulation on cytosolic Ca(2+) oscillations [Ca(2+)](c) in stimulatory glucose conditions. Our results show that both cell types respond to glucose directly in the concentration range compatible with the glucose transporters they express. The physiological ACh concentration increases the frequency of glucose stimulated [Ca(2+)](c) oscillations in both cell types and synchronizes [Ca(2+)](c) oscillations in acinar cells. The supraphysiological ACh concentration further increases the oscillation frequency on the level of individual beta cells, inhibits the synchronization between these cells, and abolishes oscillatory activity in acinar cells. We discuss possible mechanisms leading to the observed phenomena. MDPI 2021-06-23 /pmc/articles/PMC8305080/ /pubmed/34201461 http://dx.doi.org/10.3390/cells10071580 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sluga, Nastja Postić, Sandra Sarikas, Srdjan Huang, Ya-Chi Stožer, Andraž Slak Rupnik, Marjan Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title | Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title_full | Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title_fullStr | Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title_full_unstemmed | Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title_short | Dual Mode of Action of Acetylcholine on Cytosolic Calcium Oscillations in Pancreatic Beta and Acinar Cells In Situ |
title_sort | dual mode of action of acetylcholine on cytosolic calcium oscillations in pancreatic beta and acinar cells in situ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305080/ https://www.ncbi.nlm.nih.gov/pubmed/34201461 http://dx.doi.org/10.3390/cells10071580 |
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