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Cutting Edge: Regulation of Intestinal Inflammation and Barrier Function by IL-17C
Author(s) -
Joseph M. Reynolds,
Gustavo Martínez,
Kalyan C. Nallaparaju,
Seon Hee Chang,
Yi-Hong Wang,
Chen Dong
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1103014
Subject(s) - occludin , barrier function , inflammation , microbiology and biotechnology , colitis , cytokine , tight junction , immunology , biology , function (biology) , chemistry
In the IL-17 family of cytokines, much is known about the sources and functions of IL-17, IL-17F, and IL-25 in the host defense against infection and in inflammatory diseases; however, the physiological function of IL-17C remains poorly understood. Using mice deficient in IL-17C, we demonstrate that this cytokine is crucial for the regulation of an acute experimental colitis elicited by dextran sulfate sodium. In this model, mice lacking IL-17C exhibited exacerbated disease that was associated with increased IL-17 expression by γδ T cells and Th17 cells. Moreover, IL-17C directly regulated the expression of the tight junction molecule occludin by colonic epithelial cells. Thus, our data suggest that IL-17C plays a critical role in maintaining mucosal barrier integrity.

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