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Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium
The mesothelium, the lining of the coelomic cavities, and the urothelium, the inner lining of the urinary drainage system, are highly specialized epithelia that protect the underlying tissues from mechanical stress and seal them from the overlying fluid space. The development of these epithelia from...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229118/ https://www.ncbi.nlm.nih.gov/pubmed/25389758 http://dx.doi.org/10.1371/journal.pone.0112112 |
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author | Rudat, Carsten Grieskamp, Thomas Röhr, Christian Airik, Rannar Wrede, Christoph Hegermann, Jan Herrmann, Bernhard G. Schuster-Gossler, Karin Kispert, Andreas |
author_facet | Rudat, Carsten Grieskamp, Thomas Röhr, Christian Airik, Rannar Wrede, Christoph Hegermann, Jan Herrmann, Bernhard G. Schuster-Gossler, Karin Kispert, Andreas |
author_sort | Rudat, Carsten |
collection | PubMed |
description | The mesothelium, the lining of the coelomic cavities, and the urothelium, the inner lining of the urinary drainage system, are highly specialized epithelia that protect the underlying tissues from mechanical stress and seal them from the overlying fluid space. The development of these epithelia from simple precursors and the molecular characteristics of the mature tissues are poorly analyzed. Here, we show that uroplakin 3B (Upk3b), which encodes an integral membrane protein of the tetraspanin superfamily, is specifically expressed both in development as well as under homeostatic conditions in adult mice in the mesothelia of the body cavities, i.e., the epicardium and pericardium, the pleura and the peritoneum, and in the urothelium of the urinary tract. To analyze Upk3b function, we generated a creERT2 knock-in allele by homologous recombination in embryonic stem cells. We show that Upk3b(creERT2) represents a null allele despite the lack of creERT2 expression from the mutated locus. Morphological, histological and molecular analyses of Upk3b-deficient mice did not detect changes in differentiation or integrity of the urothelium and the mesothelia that cover internal organs. Upk3b is coexpressed with the closely related Upk3a gene in the urothelium but not in the mesothelium, leaving the possibility of a functional redundancy between the two genes in the urothelium only. |
format | Online Article Text |
id | pubmed-4229118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42291182014-11-18 Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium Rudat, Carsten Grieskamp, Thomas Röhr, Christian Airik, Rannar Wrede, Christoph Hegermann, Jan Herrmann, Bernhard G. Schuster-Gossler, Karin Kispert, Andreas PLoS One Research Article The mesothelium, the lining of the coelomic cavities, and the urothelium, the inner lining of the urinary drainage system, are highly specialized epithelia that protect the underlying tissues from mechanical stress and seal them from the overlying fluid space. The development of these epithelia from simple precursors and the molecular characteristics of the mature tissues are poorly analyzed. Here, we show that uroplakin 3B (Upk3b), which encodes an integral membrane protein of the tetraspanin superfamily, is specifically expressed both in development as well as under homeostatic conditions in adult mice in the mesothelia of the body cavities, i.e., the epicardium and pericardium, the pleura and the peritoneum, and in the urothelium of the urinary tract. To analyze Upk3b function, we generated a creERT2 knock-in allele by homologous recombination in embryonic stem cells. We show that Upk3b(creERT2) represents a null allele despite the lack of creERT2 expression from the mutated locus. Morphological, histological and molecular analyses of Upk3b-deficient mice did not detect changes in differentiation or integrity of the urothelium and the mesothelia that cover internal organs. Upk3b is coexpressed with the closely related Upk3a gene in the urothelium but not in the mesothelium, leaving the possibility of a functional redundancy between the two genes in the urothelium only. Public Library of Science 2014-11-12 /pmc/articles/PMC4229118/ /pubmed/25389758 http://dx.doi.org/10.1371/journal.pone.0112112 Text en © 2014 Rudat et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rudat, Carsten Grieskamp, Thomas Röhr, Christian Airik, Rannar Wrede, Christoph Hegermann, Jan Herrmann, Bernhard G. Schuster-Gossler, Karin Kispert, Andreas Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title |
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title_full |
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title_fullStr |
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title_full_unstemmed |
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title_short |
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium |
title_sort | upk3b is dispensable for development and integrity of urothelium and mesothelium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229118/ https://www.ncbi.nlm.nih.gov/pubmed/25389758 http://dx.doi.org/10.1371/journal.pone.0112112 |
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