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Published on: July 13, 2016
Ultrastructural phenotype of "intestinal-type" cells in columnar-lined esophagus
A Sbarbati1, N Faccioli, F Ricci
1Dipartimento di Scienze Morfologico-Biomediche, Università di Verona, Italy. andrea.sbarbati@univr.it
Insights
Ultrastructural analysis of columnar-lined esophagus in reflux esophagitis patients revealed diverse cell types but no true enterocytes. Findings suggest a "phenotypic shift" rather than intestinal metaplasia in Barrett's esophagus.
Area of Science:
- Gastroenterology
- Cell Biology
- Histopathology
Background:
- Columnar-lined esophagus, often seen in Barrett's esophagus, is typically described as intestinal metaplasia.
- Previous ultrastructural studies have not identified enterocytes in this condition.
Purpose of the Study:
- To investigate the morphology and histogenesis of proliferating cells in columnar-lined esophagus.
- To clarify the nature of intestinal-type epithelium in reflux esophagitis.
Main Methods:
- Ultrastructural analysis of columnar-lined mucosa from 35 patients with reflux esophagitis.
- Detailed examination of cell phenotypes and differentiation.
Main Results:
- A wide spectrum of columnar cell ultrastructural features was observed, including secretory, secretory-absorptive, and atypical cells.
- True enterocytes were not detected; secretory-absorptive cells were the most common phenotype.
- The findings suggest a phenotypic shift of undifferentiated cells, not classical intestinal metaplasia.
Conclusions:
- Ultrastructural data do not support the concept of intestinal metaplasia in columnar-lined esophagus.
- The observed cellular heterogeneity arises from a phenotypic shift, forming novel cell types.
- Barrett's specialized metaplasia may originate from cells with broad differentiation capacity.
Abstract:
An intestinal-type epithelium is often present at columnar-lined esophagus, gastroesophageal junction or within the so-called short segment Barrett's esophagus, but ultrastructural study failed to detect enterocytes in columnar-lined esophagus. The authors have analyzed the intestinal aspects present in areas of columnar-lined esophagus in a population of patients with reflux esophagitis to better understand the morphology and histogenesis of the proliferating elements. Columnar-lined mucosa was studied in 35 patients. Columnarsurface cells displayed a wide spectrum of ultrastructural features. Well-differentiated columnar secretory cells, secretory-absorptive cells, poorly differentiated columnar cells, atypical columnar cells, and goblet cells were detected. Well-differentiated absorptive cells were never found, These results demonstrate that the areas of intestinal metaplasia show a wide spectrum of ultrastructural phenotypes, ranging from poorly to well-differentiated cells. However, true enterocytes were not found and the most represented phenotype is that of secretory-absorptive cells, whose principal characteristic is the presence of secretory and absorptive aspects together. They can be described as secretory enterocytes or cells with double specialization. To the authors' knowledge, similar cells were not previously described in normal intestinal mucosa, and ultrastructural studies are consistent in describing a broad spectrum of ultrastructural features, suggesting that Barrett's specialized metaplasia is derived from cells with the capacity for a wide range of differentiation. Therefore, despite the wide use of term intestinal metaplasia in the medical literature, experimental data clearly failed to detect enterocytes in the columnar-lined esophagus, and ultrastructural data do not support the concept of intestinal metaplasia. The cellular heterogeneity seems to be the result of a "phenotypic shift" of undifferentiated elements, which show a different pattern of evolution. The result of this process is the formation of new cell types dissimilar from those normally present in esophageal, gastric, or duodenal mucosa.
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