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Publication : Interleukin-23-Independent IL-17 Production Regulates Intestinal Epithelial Permeability.

First Author  Lee JS Year  2015
Journal  Immunity Volume  43
Issue  4 Pages  727-38
PubMed ID  26431948 Mgi Jnum  J:233769
Mgi Id  MGI:5788042 Doi  10.1016/j.immuni.2015.09.003
Citation  Lee JS, et al. (2015) Interleukin-23-Independent IL-17 Production Regulates Intestinal Epithelial Permeability. Immunity 43(4):727-38
abstractText  Whether interleukin-17A (IL-17A) has pathogenic and/or protective roles in the gut mucosa is controversial and few studies have analyzed specific cell populations for protective functions within the inflamed colonic tissue. Here we have provided evidence for IL-17A-dependent regulation of the tight junction protein occludin during epithelial injury that limits excessive permeability and maintains barrier integrity. Analysis of epithelial cells showed that in the absence of signaling via the IL-17 receptor adaptor protein Act-1, the protective effect of IL-17A was abrogated and inflammation was enhanced. We have demonstrated that after acute intestinal injury, IL-23R(+) gammadelta T cells in the colonic lamina propria were the primary producers of early, gut-protective IL-17A, and this production of IL-17A was IL-23 independent, leaving protective IL-17 intact in the absence of IL-23. These results suggest that IL-17-producing gammadelta T cells are important for the maintenance and protection of epithelial barriers in the intestinal mucosa.
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