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Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier

A weakening of the gut mucous barrier permits an increase in the access of intestinal luminal contents to the epithelial cells, which will trigger the inflammatory response. In inflammatory bowel diseases, there is an inappropriate and ongoing activation of the immune system, possibly because the in...

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Autores principales: Gouyer, Valérie, Dubuquoy, Laurent, Robbe-Masselot, Catherine, Neut, Christel, Singer, Elisabeth, Plet, Ségolène, Geboes, Karel, Desreumaux, Pierre, Gottrand, Frédéric, Desseyn, Jean-Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431476/
https://www.ncbi.nlm.nih.gov/pubmed/25974250
http://dx.doi.org/10.1038/srep09577
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author Gouyer, Valérie
Dubuquoy, Laurent
Robbe-Masselot, Catherine
Neut, Christel
Singer, Elisabeth
Plet, Ségolène
Geboes, Karel
Desreumaux, Pierre
Gottrand, Frédéric
Desseyn, Jean-Luc
author_facet Gouyer, Valérie
Dubuquoy, Laurent
Robbe-Masselot, Catherine
Neut, Christel
Singer, Elisabeth
Plet, Ségolène
Geboes, Karel
Desreumaux, Pierre
Gottrand, Frédéric
Desseyn, Jean-Luc
author_sort Gouyer, Valérie
collection PubMed
description A weakening of the gut mucous barrier permits an increase in the access of intestinal luminal contents to the epithelial cells, which will trigger the inflammatory response. In inflammatory bowel diseases, there is an inappropriate and ongoing activation of the immune system, possibly because the intestinal mucus is less protective against the endogenous microflora. General strategies aimed at improving the protection of the intestinal epithelium are still missing. We generated a transgenic mouse that secreted a molecule consisting of 12 consecutive copies of a mucin domain into its intestinal mucus, which is believed to modify the mucus layer by establishing reversible interactions. We showed that the mucus gel was more robust and that mucin O-glycosylation was altered. Notably, the gut epithelium of transgenic mice housed a greater abundance of beneficial Lactobacillus spp. These modifications were associated with a reduced susceptibility of transgenic mice to chemically induced colitis. Furthermore, transgenic mice cleared faster Citrobacter rodentium bacteria which were orally given and mice were more protected against bacterial translocation induced by gavage with adherent–invasive Escherichia coli. Our data show that delivering the mucin CYS domain into the gut lumen strengthens the intestinal mucus blanket which is impaired in inflammatory bowel diseases.
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spelling pubmed-44314762015-05-22 Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier Gouyer, Valérie Dubuquoy, Laurent Robbe-Masselot, Catherine Neut, Christel Singer, Elisabeth Plet, Ségolène Geboes, Karel Desreumaux, Pierre Gottrand, Frédéric Desseyn, Jean-Luc Sci Rep Article A weakening of the gut mucous barrier permits an increase in the access of intestinal luminal contents to the epithelial cells, which will trigger the inflammatory response. In inflammatory bowel diseases, there is an inappropriate and ongoing activation of the immune system, possibly because the intestinal mucus is less protective against the endogenous microflora. General strategies aimed at improving the protection of the intestinal epithelium are still missing. We generated a transgenic mouse that secreted a molecule consisting of 12 consecutive copies of a mucin domain into its intestinal mucus, which is believed to modify the mucus layer by establishing reversible interactions. We showed that the mucus gel was more robust and that mucin O-glycosylation was altered. Notably, the gut epithelium of transgenic mice housed a greater abundance of beneficial Lactobacillus spp. These modifications were associated with a reduced susceptibility of transgenic mice to chemically induced colitis. Furthermore, transgenic mice cleared faster Citrobacter rodentium bacteria which were orally given and mice were more protected against bacterial translocation induced by gavage with adherent–invasive Escherichia coli. Our data show that delivering the mucin CYS domain into the gut lumen strengthens the intestinal mucus blanket which is impaired in inflammatory bowel diseases. Nature Publishing Group 2015-05-14 /pmc/articles/PMC4431476/ /pubmed/25974250 http://dx.doi.org/10.1038/srep09577 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gouyer, Valérie
Dubuquoy, Laurent
Robbe-Masselot, Catherine
Neut, Christel
Singer, Elisabeth
Plet, Ségolène
Geboes, Karel
Desreumaux, Pierre
Gottrand, Frédéric
Desseyn, Jean-Luc
Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title_full Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title_fullStr Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title_full_unstemmed Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title_short Delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
title_sort delivery of a mucin domain enriched in cysteine residues strengthens the intestinal mucous barrier
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431476/
https://www.ncbi.nlm.nih.gov/pubmed/25974250
http://dx.doi.org/10.1038/srep09577
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