Cargando…

A Zebrafish Model for Studies on Esophageal Epithelial Biology

Mammalian esophagus exhibits a remarkable change in epithelial structure during the transition from embryo to adult. However, the molecular mechanisms of esophageal epithelial development are not well understood. Zebrafish (Danio rerio), a common model organism for vertebrate development and gene fu...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Hao, Beasley, Andrea, Hu, Yuhui, Chen, Xiaoxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667901/
https://www.ncbi.nlm.nih.gov/pubmed/26630178
http://dx.doi.org/10.1371/journal.pone.0143878
_version_ 1782403898143670272
author Chen, Hao
Beasley, Andrea
Hu, Yuhui
Chen, Xiaoxin
author_facet Chen, Hao
Beasley, Andrea
Hu, Yuhui
Chen, Xiaoxin
author_sort Chen, Hao
collection PubMed
description Mammalian esophagus exhibits a remarkable change in epithelial structure during the transition from embryo to adult. However, the molecular mechanisms of esophageal epithelial development are not well understood. Zebrafish (Danio rerio), a common model organism for vertebrate development and gene function, has not previously been characterized as a model system for esophageal epithelial development. In this study, we characterized a piece of non-keratinized stratified squamous epithelium similar to human esophageal epithelium in the upper digestive tract of developing zebrafish. Under the microscope, this piece was detectable at 5dpf and became stratified at 7dpf. Expression of esophageal epithelial marker genes (Krt5, P63, Sox2 and Pax9) was detected by immunohistochemistry and in situ hybridization. Knockdown of P63, a gene known to be critical for esophageal epithelium, disrupted the development of this epithelium. With this model system, we found that Pax9 knockdown resulted in loss or disorganization of the squamous epithelium, as well as down-regulation of the differentiation markers Krt4 and Krt5. In summary, we characterized a region of stratified squamous epithelium in the zebrafish upper digestive tract which can be used for functional studies of candidate genes involved in esophageal epithelial biology.
format Online
Article
Text
id pubmed-4667901
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46679012015-12-10 A Zebrafish Model for Studies on Esophageal Epithelial Biology Chen, Hao Beasley, Andrea Hu, Yuhui Chen, Xiaoxin PLoS One Research Article Mammalian esophagus exhibits a remarkable change in epithelial structure during the transition from embryo to adult. However, the molecular mechanisms of esophageal epithelial development are not well understood. Zebrafish (Danio rerio), a common model organism for vertebrate development and gene function, has not previously been characterized as a model system for esophageal epithelial development. In this study, we characterized a piece of non-keratinized stratified squamous epithelium similar to human esophageal epithelium in the upper digestive tract of developing zebrafish. Under the microscope, this piece was detectable at 5dpf and became stratified at 7dpf. Expression of esophageal epithelial marker genes (Krt5, P63, Sox2 and Pax9) was detected by immunohistochemistry and in situ hybridization. Knockdown of P63, a gene known to be critical for esophageal epithelium, disrupted the development of this epithelium. With this model system, we found that Pax9 knockdown resulted in loss or disorganization of the squamous epithelium, as well as down-regulation of the differentiation markers Krt4 and Krt5. In summary, we characterized a region of stratified squamous epithelium in the zebrafish upper digestive tract which can be used for functional studies of candidate genes involved in esophageal epithelial biology. Public Library of Science 2015-12-02 /pmc/articles/PMC4667901/ /pubmed/26630178 http://dx.doi.org/10.1371/journal.pone.0143878 Text en © 2015 Chen 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
Chen, Hao
Beasley, Andrea
Hu, Yuhui
Chen, Xiaoxin
A Zebrafish Model for Studies on Esophageal Epithelial Biology
title A Zebrafish Model for Studies on Esophageal Epithelial Biology
title_full A Zebrafish Model for Studies on Esophageal Epithelial Biology
title_fullStr A Zebrafish Model for Studies on Esophageal Epithelial Biology
title_full_unstemmed A Zebrafish Model for Studies on Esophageal Epithelial Biology
title_short A Zebrafish Model for Studies on Esophageal Epithelial Biology
title_sort zebrafish model for studies on esophageal epithelial biology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667901/
https://www.ncbi.nlm.nih.gov/pubmed/26630178
http://dx.doi.org/10.1371/journal.pone.0143878
work_keys_str_mv AT chenhao azebrafishmodelforstudiesonesophagealepithelialbiology
AT beasleyandrea azebrafishmodelforstudiesonesophagealepithelialbiology
AT huyuhui azebrafishmodelforstudiesonesophagealepithelialbiology
AT chenxiaoxin azebrafishmodelforstudiesonesophagealepithelialbiology
AT chenhao zebrafishmodelforstudiesonesophagealepithelialbiology
AT beasleyandrea zebrafishmodelforstudiesonesophagealepithelialbiology
AT huyuhui zebrafishmodelforstudiesonesophagealepithelialbiology
AT chenxiaoxin zebrafishmodelforstudiesonesophagealepithelialbiology