IL-4 Regulates Skin Homeostasis and the Predisposition toward Allergic Skin Inflammation

被引:148
作者
Sehra, Sarita
Yao, Yongxue [2 ]
Howell, Michael D. [4 ]
Nguyen, Evelyn T.
Kansas, Geoffrey S. [5 ]
Leung, Donald Y. M. [4 ]
Travers, Jeffrey B. [2 ,3 ]
Kaplan, Mark H. [1 ]
机构
[1] Indiana Univ Sch Med, HB Wells Ctr Pediat Res, Dept Pediat, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Dermatol, Indianapolis, IN 46202 USA
[3] Richard L Roudebush VA Med Ctr, Indianapolis, IN 46202 USA
[4] Natl Jewish Hlth, Dept Pediat, Denver, CO 80206 USA
[5] Northwestern Univ, Sch Med, Dept Microbiol Immunol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
CONSTITUTIVELY ACTIVE STAT6; ATOPIC-DERMATITIS; TRANSGENIC MICE; TH2; CYTOKINES; IN-VIVO; EXPRESSION; FILAGGRIN; DISEASE; CELLS; BARRIER;
D O I
10.4049/jimmunol.0901860
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-4 promotes the development of Th2 cells and allergic inflammation. In atopic dermatitis lesions, IL-4 decreases the expression of multiple genes associated with innate defense, including genes in the epidermal differentiation complex (EDC) that regulate epidermal barrier function. However, it is not clear whether IL-4 also contributes to homeostatic control of EDC genes. In this report, we demonstrate that expression of EDC genes and barrier function is increased in the absence of endogenous IL-4. Mice that express a constitutively active Stat6 (Stat6VT) are prone to the development of allergic skin inflammation and have decreased expression of EDC genes. IL-4 deficiency protects Stat6VT transgenic mice from the development of allergic skin inflammation and decreased recovery time in barrier function following skin irritation, with a concomitant increase in EDC gene expression. These data suggest that IL-4 plays an important role in regulating epidermal homeostasis and innate barrier function. The Journal of Immunology, 2010, 184: 3186-3190.
引用
收藏
页码:3186 / 3190
页数:5
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