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Bacteroidales recruit IL-6 producing intraepithelial lymphocytes in the colon to promote barrier integrity

Interactions between the microbiota and distal gut are important for the maintenance of a healthy intestinal barrier; dysbiosis of intestinal microbial communities has emerged as a likely contributor to diseases that arise at the level of the mucosa. Intraepithelial lymphocytes (IELs) are positioned...

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Detalles Bibliográficos
Autores principales: Kuhn, Kristine A., Schulz, Hanna M., Regner, Emilie H., Severs, Erin L., Hendrickson, Jason D., Mehta, Gaurav, Whitney, Alyssa K., Ir, Diana, Ohri, Neha, Robertson, Charles E., Frank, Daniel N., Campbell, Eric L., Colgan, Sean P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815964/
https://www.ncbi.nlm.nih.gov/pubmed/28812548
http://dx.doi.org/10.1038/mi.2017.55
Descripción
Sumario:Interactions between the microbiota and distal gut are important for the maintenance of a healthy intestinal barrier; dysbiosis of intestinal microbial communities has emerged as a likely contributor to diseases that arise at the level of the mucosa. Intraepithelial lymphocytes (IELs) are positioned within the epithelial barrier, and in the small intestine, function to maintain epithelial homeostasis. We hypothesized that colonic IELs promote epithelial barrier function through the expression of cytokines in response to interactions with commensal bacteria. 16S rRNA profiling revealed that candidate bacteria in the order Bacteroidales are sufficient to promote IEL presence in the colon, which in turn, produce IL-6 in a MyD88-dependent fashion. IEL-derived IL-6 is functionally important in the maintenance of the epithelial barrier as IL-6(−/−) mice were noted to have increased paracellular permeability, decreased claudin-1 expression, and a thinner mucus-gel layer, all of which were reversed by transfer of IL-6(+/+) IELs, leading to protection of mice in response to Citrobacter rodentium infection. Therefore, we conclude that microbiota provide a homeostatic role for epithelial barrier function through regulation of IEL-derived IL-6.