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Bile Salts at Low pH Cause Dilation of Intercellular Spaces in In Vitro Stratified Primary Esophageal Cells, Possibly by Modulating Wnt Signaling

Overview of attention for article published in Journal of Gastrointestinal Surgery, December 2015
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Title
Bile Salts at Low pH Cause Dilation of Intercellular Spaces in In Vitro Stratified Primary Esophageal Cells, Possibly by Modulating Wnt Signaling
Published in
Journal of Gastrointestinal Surgery, December 2015
DOI 10.1007/s11605-015-3062-2
Pubmed ID
Authors

Sayak Ghatak, Marie Reveiller, Liana Toia, Andrei I Ivanov, Zhongren Zhou, Eileen M Redmond, Tony E Godfrey, Jeffrey H Peters

Abstract

The presence of dilated intercellular spaces in the stratified squamous lining of the esophagus is the pathognomonic feature of reflux esophagitis secondary to gastroesophageal reflux disease (GERD). In addition to stomach acid, bile salts are major constituents of gastroesophageal refluxate. The aim of our study was to determine the effect of bile salts cocktail at different pHs on epithelial junctions in an in vitro transwell model of stratified esophageal squamous epithelium. Human telomerase reverse transcriptase (hTERT) immortalized primary esophageal EPC1 cells were grown on polyester transwell surfaces in calcium-enriched media. The cells exhibited gradual stratification into an 11-layered squamous epithelium over 7 days, together with epithelial barrier function as indicated by increased transepithelial electrical resistance (TEER). This stratified epithelium demonstrated well-formed tight junctions, adherens junctions, and desmosomes as visualized by immunofluorescence and electron microscopy. When exposed to short pulses of bile salts at pH 5, but not either condition alone, there was loss of stratification and decrease in TEER, concomitant with disruption of adherens junctions, tight junctions, and desmosomes, leading to the appearance of dilated intercellular spaces. At the cellular level, bile salts at pH 5 activated the Wnt pathway (indicated by increased β-catenin Ser552 phosphorylation). In conclusion, in our in vitro transwell model bile salts at pH 5, but not bile salts or media at pH 5 alone, modulate Wnt signaling, disrupt different junctional complexes, and cause increased permeability of stratified squamous esophageal epithelium. These changes approximate the appearance of dilated intercellular space similar to that found in GERD patients.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 6%
Unknown 15 94%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 25%
Student > Doctoral Student 3 19%
Student > Bachelor 2 13%
Student > Postgraduate 2 13%
Professor > Associate Professor 2 13%
Other 1 6%
Unknown 2 13%
Readers by discipline Count As %
Medicine and Dentistry 8 50%
Biochemistry, Genetics and Molecular Biology 4 25%
Chemical Engineering 2 13%
Unknown 2 13%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 December 2015.
All research outputs
#22,758,309
of 25,373,627 outputs
Outputs from Journal of Gastrointestinal Surgery
#2,082
of 2,485 outputs
Outputs of similar age
#341,763
of 399,580 outputs
Outputs of similar age from Journal of Gastrointestinal Surgery
#48
of 70 outputs
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