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Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release
In the gastrointestinal (GI) epithelium, enterochromaffin (EC) cells are enteroendocrine cells responsible for producing >90% of the body’s serotonin (5-hydroxytryptamine, 5-HT). However, the molecular mechanisms of EC cell function are poorly understood. Here, we found that EC cells in mouse pri...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688111/ https://www.ncbi.nlm.nih.gov/pubmed/29142310 http://dx.doi.org/10.1038/s41598-017-15834-3 |
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author | Strege, Peter R. Knutson, Kaitlyn Eggers, Samuel J. Li, Joyce H. Wang, Fan Linden, David Szurszewski, Joseph H. Milescu, Lorin Leiter, Andrew B. Farrugia, Gianrico Beyder, Arthur |
author_facet | Strege, Peter R. Knutson, Kaitlyn Eggers, Samuel J. Li, Joyce H. Wang, Fan Linden, David Szurszewski, Joseph H. Milescu, Lorin Leiter, Andrew B. Farrugia, Gianrico Beyder, Arthur |
author_sort | Strege, Peter R. |
collection | PubMed |
description | In the gastrointestinal (GI) epithelium, enterochromaffin (EC) cells are enteroendocrine cells responsible for producing >90% of the body’s serotonin (5-hydroxytryptamine, 5-HT). However, the molecular mechanisms of EC cell function are poorly understood. Here, we found that EC cells in mouse primary cultures fired spontaneous bursts of action potentials. We examined the repertoire of voltage-gated sodium channels (Na(V)) in fluorescence-sorted mouse EC cells and found that Scn3a was highly expressed. Scn3a-encoded Na(V)1.3 was specifically and densely expressed at the basal side of both human and mouse EC cells. Using electrophysiology, we found that EC cells expressed robust Na(V)1.3 currents, as determined by their biophysical and pharmacologic properties. Na(V)1.3 was not only critical for generating action potentials in EC cells, but it was also important for regulating 5-HT release by these cells. Therefore, EC cells use Scn3a-encoded voltage-gated sodium channel Na(V)1.3 for electrical excitability and 5-HT release. Na(V)1.3-dependent electrical excitability and its contribution to 5-HT release is a novel mechanism of EC cell function. |
format | Online Article Text |
id | pubmed-5688111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56881112017-11-24 Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release Strege, Peter R. Knutson, Kaitlyn Eggers, Samuel J. Li, Joyce H. Wang, Fan Linden, David Szurszewski, Joseph H. Milescu, Lorin Leiter, Andrew B. Farrugia, Gianrico Beyder, Arthur Sci Rep Article In the gastrointestinal (GI) epithelium, enterochromaffin (EC) cells are enteroendocrine cells responsible for producing >90% of the body’s serotonin (5-hydroxytryptamine, 5-HT). However, the molecular mechanisms of EC cell function are poorly understood. Here, we found that EC cells in mouse primary cultures fired spontaneous bursts of action potentials. We examined the repertoire of voltage-gated sodium channels (Na(V)) in fluorescence-sorted mouse EC cells and found that Scn3a was highly expressed. Scn3a-encoded Na(V)1.3 was specifically and densely expressed at the basal side of both human and mouse EC cells. Using electrophysiology, we found that EC cells expressed robust Na(V)1.3 currents, as determined by their biophysical and pharmacologic properties. Na(V)1.3 was not only critical for generating action potentials in EC cells, but it was also important for regulating 5-HT release by these cells. Therefore, EC cells use Scn3a-encoded voltage-gated sodium channel Na(V)1.3 for electrical excitability and 5-HT release. Na(V)1.3-dependent electrical excitability and its contribution to 5-HT release is a novel mechanism of EC cell function. Nature Publishing Group UK 2017-11-15 /pmc/articles/PMC5688111/ /pubmed/29142310 http://dx.doi.org/10.1038/s41598-017-15834-3 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Strege, Peter R. Knutson, Kaitlyn Eggers, Samuel J. Li, Joyce H. Wang, Fan Linden, David Szurszewski, Joseph H. Milescu, Lorin Leiter, Andrew B. Farrugia, Gianrico Beyder, Arthur Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title | Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title_full | Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title_fullStr | Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title_full_unstemmed | Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title_short | Sodium channel Na(V)1.3 is important for enterochromaffin cell excitability and serotonin release |
title_sort | sodium channel na(v)1.3 is important for enterochromaffin cell excitability and serotonin release |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688111/ https://www.ncbi.nlm.nih.gov/pubmed/29142310 http://dx.doi.org/10.1038/s41598-017-15834-3 |
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