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The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine

The large intestine plays a pivotal role in water and electrolyte balance. Paracellular transport may play a role in ion transport mechanisms in the cecum and large intestine; however, these molecular mechanisms and their physiological roles have not been fully studied. Claudin-15 forms a cation cha...

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Autores principales: Hempstock, Wendy, Nagata, Nozomi, Ishizuka, Noriko, Hayashi, Hisayoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133298/
https://www.ncbi.nlm.nih.gov/pubmed/37100833
http://dx.doi.org/10.1038/s41598-023-33431-5
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author Hempstock, Wendy
Nagata, Nozomi
Ishizuka, Noriko
Hayashi, Hisayoshi
author_facet Hempstock, Wendy
Nagata, Nozomi
Ishizuka, Noriko
Hayashi, Hisayoshi
author_sort Hempstock, Wendy
collection PubMed
description The large intestine plays a pivotal role in water and electrolyte balance. Paracellular transport may play a role in ion transport mechanisms in the cecum and large intestine; however, these molecular mechanisms and their physiological roles have not been fully studied. Claudin-15 forms a cation channel in tight junctions in the small intestine, but its role in the cecum and large intestine has not been investigated. This study aimed to explore the physiological role of claudin-15 in the cecum and large intestine using claudin-15 (Cldn15) KO mice. Electrical conductance, short-circuit current, Na(+) flux, and dilution potential were assessed in isolated tissue preparations mounted in Ussing chambers. The induced short-circuit current of short-chain fatty acids, which are fermentative products in the intestinal tract, was also measured. Compared to wild type mice, the electrical conductance and paracellular Na(+) flux was decreased in the cecum, but not the middle large intestine, while in both the cecum and the middle large intestine, paracellular Na(+) permeability was decreased in Cldn15 KO mice. These results suggest that claudin-15 is responsible for Na(+) permeability in the tight junctions of the cecum and large intestine and decreased Na(+) permeability in the cecum may cause impaired absorption function.
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spelling pubmed-101332982023-04-28 The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine Hempstock, Wendy Nagata, Nozomi Ishizuka, Noriko Hayashi, Hisayoshi Sci Rep Article The large intestine plays a pivotal role in water and electrolyte balance. Paracellular transport may play a role in ion transport mechanisms in the cecum and large intestine; however, these molecular mechanisms and their physiological roles have not been fully studied. Claudin-15 forms a cation channel in tight junctions in the small intestine, but its role in the cecum and large intestine has not been investigated. This study aimed to explore the physiological role of claudin-15 in the cecum and large intestine using claudin-15 (Cldn15) KO mice. Electrical conductance, short-circuit current, Na(+) flux, and dilution potential were assessed in isolated tissue preparations mounted in Ussing chambers. The induced short-circuit current of short-chain fatty acids, which are fermentative products in the intestinal tract, was also measured. Compared to wild type mice, the electrical conductance and paracellular Na(+) flux was decreased in the cecum, but not the middle large intestine, while in both the cecum and the middle large intestine, paracellular Na(+) permeability was decreased in Cldn15 KO mice. These results suggest that claudin-15 is responsible for Na(+) permeability in the tight junctions of the cecum and large intestine and decreased Na(+) permeability in the cecum may cause impaired absorption function. Nature Publishing Group UK 2023-04-26 /pmc/articles/PMC10133298/ /pubmed/37100833 http://dx.doi.org/10.1038/s41598-023-33431-5 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hempstock, Wendy
Nagata, Nozomi
Ishizuka, Noriko
Hayashi, Hisayoshi
The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title_full The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title_fullStr The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title_full_unstemmed The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title_short The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
title_sort effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133298/
https://www.ncbi.nlm.nih.gov/pubmed/37100833
http://dx.doi.org/10.1038/s41598-023-33431-5
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