Abstract
The intestinal barrier is formed by a monolayer of columnar epithelial cells. This barrier is effectively maintained despite the high turnover of epithelial cells in the gut. Defects in the mechanism by which barrier function is maintained are believed to play a central role in the pathogenesis of inflammatory bowel disease (IBD). Proinflammatory cytokines such as TNF-α and IFN-γ are often elevated in inflamed tissue of patients with IBD. In fact, anti-TNF-α therapy is routinely administered to patients with Crohn’s disease. We have previously demonstrated that intestinal epithelial cells are shed from the intestine leaving a ‘gap’ in the epithelium that is able to maintain barrier function. The rate of cell shedding and barrier permeability is substantially increased by the administration of TNF-α. Loss of barrier function at the site of a gap may provide a site of entry for disease-causing bacteria.
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Acknowledgments
The authors would like to thank Dr Ralph Kiesslich from The University of Mainz, Germany for adapting the confocal endoscopy technique in the human.
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Duckworth, C.A., Watson, A.J. (2011). Analysis of Epithelial Cell Shedding and Gaps in the Intestinal Epithelium. In: Turksen, K. (eds) Permeability Barrier. Methods in Molecular Biology, vol 763. Humana Press. https://doi.org/10.1007/978-1-61779-191-8_7
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DOI: https://doi.org/10.1007/978-1-61779-191-8_7
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