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Publication : The severity of imiquimod-induced mouse skin inflammation is independent of endogenous IL-38 expression.

First Author  Palomo J Year  2018
Journal  PLoS One Volume  13
Issue  3 Pages  e0194667
PubMed ID  29554104 Mgi Jnum  J:260118
Mgi Id  MGI:6148505 Doi  10.1371/journal.pone.0194667
Citation  Palomo J, et al. (2018) The severity of imiquimod-induced mouse skin inflammation is independent of endogenous IL-38 expression. PLoS One 13(3):e0194667
abstractText  The IL-1 cytokine family includes eleven members, among which Il-36alpha, beta and gamma, IL-36Ra and IL-38. The IL-36 cytokines are involved in the pathogenesis of psoriasis. IL-38 is also expressed in the skin and was previously proposed to act as an IL-36 antagonist. In this study, we thus examined expression and function of Il-38 in a mouse model of imiquimod (IMQ)-induced skin inflammation. Il-38 mRNA was detected in the epidermis and in primary mouse keratinocytes, but not in dermal fibroblasts. At the peak of IMQ-induced inflammation, skin Il-38 mRNA levels were reduced, whereas Il-36ra mRNA expression increased. The severity of IMQ-induced skin inflammation, as assessed by recording ear thickness and histological changes, was similar in Il-38 KO and WT littermate control mice, while, in contrast, Il-36ra-deficient mice displayed more severe skin pathology than their WT littermates. Il-38-deficiency had no impact on IMQ-induced expression of proinflammatory mediators in the skin in vivo, on the basal expression of various cytokines or chemokines by cultured primary keratinocytes and dermal fibroblasts in vitro, or on the response of these cells to Il-36beta. Finally, after cessation of topical IMQ application, the resolution of skin inflammation was also not altered in Il-38 KO mice. In conclusion, Il-38-deficiency did not impact the development or resolution of IMQ-induced skin inflammation. Our observations further suggest that endogenous Il-38 does not exert Il-36 inhibitory activity in this model, or in cultured skin cells. A potential anti-inflammatory function of Il-38 in mouse skin thus still remains to be demonstrated.
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