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Claudin-2-dependent paracellular channels are dynamically gated
Intercellular tight junctions form selectively permeable barriers that seal the paracellular space. Trans-tight junction flux has been measured across large epithelial surfaces, but conductance across individual channels has never been measured. We report a novel trans-tight junction patch clamp tec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755754/ https://www.ncbi.nlm.nih.gov/pubmed/26568313 http://dx.doi.org/10.7554/eLife.09906 |
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author | Weber, Christopher R Liang, Guo Hua Wang, Yitang Das, Sudipto Shen, Le Yu, Alan S L Nelson, Deborah J Turner, Jerrold R |
author_facet | Weber, Christopher R Liang, Guo Hua Wang, Yitang Das, Sudipto Shen, Le Yu, Alan S L Nelson, Deborah J Turner, Jerrold R |
author_sort | Weber, Christopher R |
collection | PubMed |
description | Intercellular tight junctions form selectively permeable barriers that seal the paracellular space. Trans-tight junction flux has been measured across large epithelial surfaces, but conductance across individual channels has never been measured. We report a novel trans-tight junction patch clamp technique that detects flux across individual claudin-2 channels within the tight junction of cultured canine renal tubule or human intestinal epithelial monolayers. In both cells, claudin-2 channels display conductances of ~90 pS. The channels are gated, strictly dependent on claudin-2 expression, and display size- and charge-selectivity typical of claudin-2. Kinetic analyses indicate one open and two distinct closed states. Conductance is symmetrical and reversible, characteristic of a passive, paracellular process, and blocked by reduced temperature or site-directed mutagenesis and chemical derivatization of the claudin-2 pore. We conclude that claudin-2 forms gated paracellular channels and speculate that modulation of tight junction channel gating kinetics may be an unappreciated mechanism of barrier regulation. DOI: http://dx.doi.org/10.7554/eLife.09906.001 |
format | Online Article Text |
id | pubmed-4755754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47557542016-02-18 Claudin-2-dependent paracellular channels are dynamically gated Weber, Christopher R Liang, Guo Hua Wang, Yitang Das, Sudipto Shen, Le Yu, Alan S L Nelson, Deborah J Turner, Jerrold R eLife Biophysics and Structural Biology Intercellular tight junctions form selectively permeable barriers that seal the paracellular space. Trans-tight junction flux has been measured across large epithelial surfaces, but conductance across individual channels has never been measured. We report a novel trans-tight junction patch clamp technique that detects flux across individual claudin-2 channels within the tight junction of cultured canine renal tubule or human intestinal epithelial monolayers. In both cells, claudin-2 channels display conductances of ~90 pS. The channels are gated, strictly dependent on claudin-2 expression, and display size- and charge-selectivity typical of claudin-2. Kinetic analyses indicate one open and two distinct closed states. Conductance is symmetrical and reversible, characteristic of a passive, paracellular process, and blocked by reduced temperature or site-directed mutagenesis and chemical derivatization of the claudin-2 pore. We conclude that claudin-2 forms gated paracellular channels and speculate that modulation of tight junction channel gating kinetics may be an unappreciated mechanism of barrier regulation. DOI: http://dx.doi.org/10.7554/eLife.09906.001 eLife Sciences Publications, Ltd 2015-11-14 /pmc/articles/PMC4755754/ /pubmed/26568313 http://dx.doi.org/10.7554/eLife.09906 Text en © 2015, Weber et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Weber, Christopher R Liang, Guo Hua Wang, Yitang Das, Sudipto Shen, Le Yu, Alan S L Nelson, Deborah J Turner, Jerrold R Claudin-2-dependent paracellular channels are dynamically gated |
title | Claudin-2-dependent paracellular channels are dynamically gated |
title_full | Claudin-2-dependent paracellular channels are dynamically gated |
title_fullStr | Claudin-2-dependent paracellular channels are dynamically gated |
title_full_unstemmed | Claudin-2-dependent paracellular channels are dynamically gated |
title_short | Claudin-2-dependent paracellular channels are dynamically gated |
title_sort | claudin-2-dependent paracellular channels are dynamically gated |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755754/ https://www.ncbi.nlm.nih.gov/pubmed/26568313 http://dx.doi.org/10.7554/eLife.09906 |
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