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Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin
Hearing and balance functions of the inner ear rely on the homeostasis of the endolymphatic fluid. When disturbed, pathologic endolymphatic hydrops evolves as observed in Menière’s disease. The molecular basis of inner ear fluid regulation across the endolymphatic epithelium is largely unknown. In t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379655/ https://www.ncbi.nlm.nih.gov/pubmed/28374851 http://dx.doi.org/10.1038/srep45482 |
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author | Runggaldier, Daniel Pradas, Lidia Garcia Neckel, Peter H. Mack, Andreas F. Hirt, Bernhard Gleiser, Corinna |
author_facet | Runggaldier, Daniel Pradas, Lidia Garcia Neckel, Peter H. Mack, Andreas F. Hirt, Bernhard Gleiser, Corinna |
author_sort | Runggaldier, Daniel |
collection | PubMed |
description | Hearing and balance functions of the inner ear rely on the homeostasis of the endolymphatic fluid. When disturbed, pathologic endolymphatic hydrops evolves as observed in Menière’s disease. The molecular basis of inner ear fluid regulation across the endolymphatic epithelium is largely unknown. In this study we identified the specific expression of the tight junction (TJ) molecules Claudin 3, 4, 6, 7, 8, 10, and 16 in epithelial preparations of the rat inner ear endolymphatic duct (ED) and endolymphatic sac (ES) by high-throughput qPCR and immunofluorescence confocal microscopy. Further we showed that Claudin 4 in the ES is a target of arginine-vasopressin (AVP), a hormone elevated in Menière’s disease. Moreover, our transmission-electron microscopy (TEM) analysis revealed that the TJs of the ED were shallow and shorter compared to the TJ of the ES indicating facilitation of a paracellular fluid transport across the ED epithelium. The significant differences in the subcellular localization of the barrier-forming protein Claudin 3 between the ED and ES epithelium further support the TEM observations. Our results indicate a high relevance of Claudin 3 and Claudin 4 as important paracellular barrier molecules in the ED and ES epithelium with potential involvement in the pathophysiology of Menière’s disease. |
format | Online Article Text |
id | pubmed-5379655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53796552017-04-07 Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin Runggaldier, Daniel Pradas, Lidia Garcia Neckel, Peter H. Mack, Andreas F. Hirt, Bernhard Gleiser, Corinna Sci Rep Article Hearing and balance functions of the inner ear rely on the homeostasis of the endolymphatic fluid. When disturbed, pathologic endolymphatic hydrops evolves as observed in Menière’s disease. The molecular basis of inner ear fluid regulation across the endolymphatic epithelium is largely unknown. In this study we identified the specific expression of the tight junction (TJ) molecules Claudin 3, 4, 6, 7, 8, 10, and 16 in epithelial preparations of the rat inner ear endolymphatic duct (ED) and endolymphatic sac (ES) by high-throughput qPCR and immunofluorescence confocal microscopy. Further we showed that Claudin 4 in the ES is a target of arginine-vasopressin (AVP), a hormone elevated in Menière’s disease. Moreover, our transmission-electron microscopy (TEM) analysis revealed that the TJs of the ED were shallow and shorter compared to the TJ of the ES indicating facilitation of a paracellular fluid transport across the ED epithelium. The significant differences in the subcellular localization of the barrier-forming protein Claudin 3 between the ED and ES epithelium further support the TEM observations. Our results indicate a high relevance of Claudin 3 and Claudin 4 as important paracellular barrier molecules in the ED and ES epithelium with potential involvement in the pathophysiology of Menière’s disease. Nature Publishing Group 2017-04-04 /pmc/articles/PMC5379655/ /pubmed/28374851 http://dx.doi.org/10.1038/srep45482 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Runggaldier, Daniel Pradas, Lidia Garcia Neckel, Peter H. Mack, Andreas F. Hirt, Bernhard Gleiser, Corinna Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title | Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title_full | Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title_fullStr | Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title_full_unstemmed | Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title_short | Claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
title_sort | claudin expression in the rat endolymphatic duct and sac - first insights into regulation of the paracellular barrier by vasopressin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379655/ https://www.ncbi.nlm.nih.gov/pubmed/28374851 http://dx.doi.org/10.1038/srep45482 |
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