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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...

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Autores principales: Sluga, Nastja, Postić, Sandra, Sarikas, Srdjan, Huang, Ya-Chi, Stožer, Andraž, Slak Rupnik, Marjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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