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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...

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Autores principales: Rudat, Carsten, Grieskamp, Thomas, Röhr, Christian, Airik, Rannar, Wrede, Christoph, Hegermann, Jan, Herrmann, Bernhard G., Schuster-Gossler, Karin, Kispert, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
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.
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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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