Relevance of Ultrastructural Alterations of Intercellular Junction Morphology in Inflamed Human Esophagus.
- Author:
Chia Chin LIU
1
;
Jeng Woei LEE
;
Tso Tsai LIU
;
Chih Hsun YI
;
Chien Lin CHEN
Author Information
1. Department of Life Sciences, Tzu Chi University, Hualien, Taiwan.
- Publication Type:Original Article
- Keywords:
Extracellular space;
Gastroesophageal reflux;
Microscopy, Electron, Transmission;
Tight junctions
- MeSH:
Biopsy;
Claudin-2;
Epithelium;
Esophagogastric Junction;
Esophagus;
Extracellular Space;
Gastroesophageal Reflux;
Humans;
Immunohistochemistry;
Intercellular Junctions;
Microscopy, Electron, Transmission;
Mucous Membrane;
Tight Junction Proteins;
Tight Junctions
- From:Journal of Neurogastroenterology and Motility
2013;19(3):324-331
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND/AIMS: Detailed characterization of the ultrastructural morphology of intercellular space in gastroesophageal reflux disease has not been fully studied. We aimed to investigate whether subtle alteration in intercellular space structure and tight junction proteins might differ among patients with gastroesophageal reflux disease. METHODS: Esophageal biopsies at 5 cm above the gastroesophageal junction were obtained from 6 asymptomatic controls, 10 patients with reflux symptoms but without erosions, and 18 patients with erosions. The biopsies were morphologically evaluated by transmission electron microscopy, and by using immunohistochemistry for tight junction proteins (claudin-1 and claudin-2 proteins). RESULTS: The expressions of tight junction proteins did not differ between asymptomatic controls and gastroesophageal reflux disease patients. In patients with gastroesophageal reflux disease, altered desmosomal junction morphology was only found in upper stratified squamous epithelium. Dilated intercellular space occurred only in upper stratified squamous epithelium and in patients with erosive esophagitis. CONCLUSIONS: This study suggests that dilated intercellular space may not be uniformly present inside the esophageal mucosa and predominantly it is located in upper squamous epithelium. Presence of desmosomal junction alterations is associated with increased severity of gastroesophageal reflux disease. Besides dilated intercellular space, subtle changes in ultrastructural morphology of intercellular space allow better identification of inflamed esophageal mucosa relevant to acid reflux.
