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...

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Main Authors: Hao Chen, Andrea Beasley, Yuhui Hu, Xiaoxin Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4667901?pdf=render
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spelling doaj-ec4b7800a69545809944bc3f3f8994262020-11-25T01:52:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011012e014387810.1371/journal.pone.0143878A Zebrafish Model for Studies on Esophageal Epithelial Biology.Hao ChenAndrea BeasleyYuhui HuXiaoxin ChenMammalian 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.http://europepmc.org/articles/PMC4667901?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hao Chen
Andrea Beasley
Yuhui Hu
Xiaoxin Chen
spellingShingle Hao Chen
Andrea Beasley
Yuhui Hu
Xiaoxin Chen
A Zebrafish Model for Studies on Esophageal Epithelial Biology.
PLoS ONE
author_facet Hao Chen
Andrea Beasley
Yuhui Hu
Xiaoxin Chen
author_sort Hao Chen
title A Zebrafish Model for Studies on Esophageal Epithelial Biology.
title_short 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_sort zebrafish model for studies on esophageal epithelial biology.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
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.
url http://europepmc.org/articles/PMC4667901?pdf=render
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AT andreabeasley zebrafishmodelforstudiesonesophagealepithelialbiology
AT yuhuihu zebrafishmodelforstudiesonesophagealepithelialbiology
AT xiaoxinchen zebrafishmodelforstudiesonesophagealepithelialbiology
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