[PDF][PDF] Epithelial IL-18 equilibrium controls barrier function in colitis

R Nowarski, R Jackson, N Gagliani, MR de Zoete… - Cell, 2015 - cell.com
R Nowarski, R Jackson, N Gagliani, MR de Zoete, NW Palm, W Bailis, JS Low, CCD Harman…
Cell, 2015cell.com
The intestinal mucosal barrier controlling the resident microbiome is dependent on a
protective mucus layer generated by goblet cells, impairment of which is a hallmark of the
inflammatory bowel disease, ulcerative colitis. Here, we show that IL-18 is critical in driving
the pathologic breakdown of barrier integrity in a model of colitis. Deletion of Il18 or its
receptor Il18r1 in intestinal epithelial cells (Δ/EC) conferred protection from colitis and
mucosal damage in mice. In contrast, deletion of the IL-18 negative regulator Il18bp resulted …
Summary
The intestinal mucosal barrier controlling the resident microbiome is dependent on a protective mucus layer generated by goblet cells, impairment of which is a hallmark of the inflammatory bowel disease, ulcerative colitis. Here, we show that IL-18 is critical in driving the pathologic breakdown of barrier integrity in a model of colitis. Deletion of Il18 or its receptor Il18r1 in intestinal epithelial cells (Δ/EC) conferred protection from colitis and mucosal damage in mice. In contrast, deletion of the IL-18 negative regulator Il18bp resulted in severe colitis associated with loss of mature goblet cells. Colitis and goblet cell loss were rescued in Il18bp−/−;Il18rΔ/EC mice, demonstrating that colitis severity is controlled at the level of IL-18 signaling in intestinal epithelial cells. IL-18 inhibited goblet cell maturation by regulating the transcriptional program instructing goblet cell development. These results inform on the mechanism of goblet cell dysfunction that underlies the pathology of ulcerative colitis.
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