IL-4 dysregulates microRNAs involved in inflammation, angiogenesis and apoptosis in epidermal keratinocytes

被引:12
作者
Bao, Lei [1 ]
Chau, Cecilia [2 ]
Bao, Jeremy [1 ]
Tsoukas, Maria M. [1 ]
Chan, Lawrence S. [1 ,3 ,4 ]
机构
[1] Univ Illinois, Dept Dermatol, RM 338,MC624,808 S Wood St, Chicago, IL 60612 USA
[2] Univ Illinois, Res Resources Ctr, 832 South Wolcott Ave, Chicago, IL USA
[3] Jesse Brown Vet Affairs Hosp, Med Serv, 820 S Damen Ave, Chicago, IL 60612 USA
[4] Captain James A Lovell Fed Hlth Care Ctr, Med Serv, 3001 Green Bay Rd, N Chicago, IL 60064 USA
关键词
atopic dermatitis; IL-4; keratinocytes; microRNA; REGULATES CELL-PROLIFERATION; ATOPIC-DERMATITIS; TRANSGENIC MICE; PATHOGENESIS; EXPRESSION; DISEASE; GROWTH; CANCER; GENES;
D O I
10.1111/1348-0421.12650
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 plays an important role in the pathogenesis of atopic dermatitis (AD) by dysregulating many key factors at the transcriptional level. In this study, a microRNA array technique and IL-4 transgenic mice were used to demonstrate that IL-4 dysregulates microRNAs involved in inflammation, angiogenesis, lymphangiogenesis and apoptosis. Of the 372 common microRNAs examined, 26 and one microRNAs were found to be up- and down-regulated, respectively. MicroRNA-101-5p, -122-5p, -142-3p, -204-5p, -335-3p, -376a-3p, -378a-5p, -639 and -9-5p are among the most significantly up-regulated microRNAs. MicroRNA-147a, the only one that was down- regulated in the present study, attenuates TLR-induced inflammatory responses. These dysregulated microRNAs may provide post-transcriptional regulation of key genes in AD.
引用
收藏
页码:732 / 736
页数:5
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