The intestinal epithelial barrier (IEB) is one of the largest interfaces between the environment and the internal milieu of the body. It is essential to limit the passage of harmful antigens and microorganisms and, on the other side, to assure the absorption of nutrients and water. The maintenance of this delicate equilibrium is tightly regulated as it is essential for human homeostasis. Luminal solutes and ions can pass across the IEB via two main routes: the transcellular pathway or the paracellular pathway. Tight junctions (TJs) are a multi-protein complex responsible for the regulation of paracellular permeability. TJs control the passage of antigens through the IEB and have a key role in maintaining barrier integrity. Several factors, including cytokines, gut microbiota, and dietary components are known to regulate intestinal TJs. Gut microbiota participates in several human functions including the modulation of epithelial cells and immune system through the release of several metabolites, such as short-chain fatty acids (SCFAs). Mediators released by immune cells can induce epithelial cell damage and TJs dysfunction. The subsequent disruption of the IEB allows the passage of antigens into the mucosa leading to further inflammation. Growing evidence indicates that dysbiosis, immune activation, and IEB dysfunction have a role in several diseases, including irritable bowel syndrome (IBS), inflammatory bowel disease (IBD), and gluten-related conditions. Here we summarize the interplay between the IEB and gut microbiota and mucosal immune system and their involvement in IBS, IBD, and gluten-related disorders.

Inflammatory and Microbiota-Related Regulation of the Intestinal Epithelial Barrier / Barbara G.; Barbaro M.R.; Fuschi D.; Palombo M.; Falangone F.; Cremon C.; Marasco G.; Stanghellini V.. - In: FRONTIERS IN NUTRITION. - ISSN 2296-861X. - ELETTRONICO. - 8:(2021), pp. 718356.1-718356.24. [10.3389/fnut.2021.718356]

Inflammatory and Microbiota-Related Regulation of the Intestinal Epithelial Barrier

Barbara G.;Barbaro M. R.;Fuschi D.;Palombo M.;Marasco G.;Stanghellini V.
2021

Abstract

The intestinal epithelial barrier (IEB) is one of the largest interfaces between the environment and the internal milieu of the body. It is essential to limit the passage of harmful antigens and microorganisms and, on the other side, to assure the absorption of nutrients and water. The maintenance of this delicate equilibrium is tightly regulated as it is essential for human homeostasis. Luminal solutes and ions can pass across the IEB via two main routes: the transcellular pathway or the paracellular pathway. Tight junctions (TJs) are a multi-protein complex responsible for the regulation of paracellular permeability. TJs control the passage of antigens through the IEB and have a key role in maintaining barrier integrity. Several factors, including cytokines, gut microbiota, and dietary components are known to regulate intestinal TJs. Gut microbiota participates in several human functions including the modulation of epithelial cells and immune system through the release of several metabolites, such as short-chain fatty acids (SCFAs). Mediators released by immune cells can induce epithelial cell damage and TJs dysfunction. The subsequent disruption of the IEB allows the passage of antigens into the mucosa leading to further inflammation. Growing evidence indicates that dysbiosis, immune activation, and IEB dysfunction have a role in several diseases, including irritable bowel syndrome (IBS), inflammatory bowel disease (IBD), and gluten-related conditions. Here we summarize the interplay between the IEB and gut microbiota and mucosal immune system and their involvement in IBS, IBD, and gluten-related disorders.
2021
Inflammatory and Microbiota-Related Regulation of the Intestinal Epithelial Barrier / Barbara G.; Barbaro M.R.; Fuschi D.; Palombo M.; Falangone F.; Cremon C.; Marasco G.; Stanghellini V.. - In: FRONTIERS IN NUTRITION. - ISSN 2296-861X. - ELETTRONICO. - 8:(2021), pp. 718356.1-718356.24. [10.3389/fnut.2021.718356]
Barbara G.; Barbaro M.R.; Fuschi D.; Palombo M.; Falangone F.; Cremon C.; Marasco G.; Stanghellini V.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/838937
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