| Literature DB >> 26914146 |
Mirim Jang1, Hyemin Kim1,2, Yejin Kim1, Jiyea Choi1, Jane Jeon1, Youngil Hwang1, Jae Seung Kang1,2, Wang Jae Lee1.
Abstract
House dust mite (HDM) is known as one of the factors that causes atopic dermatitis (AD). Interleukin (IL)-22 and thymus and activation regulated chemokine (TARC) are related to skin inflammatory disease and highly expressed in AD lesions. However, the effects of HDM on IL-22 production in T cells and on TARC production and IL-22Rα receptor expression in keratinocytes are unknown. To identify the role of HDM in keratinocytes and T cells, we investigated IL-22Rα expression and TARC production in the human keratinocyte cell line HaCaT and IL-22 production in T cells treated with HDM extract as well as their roles in HDM-induced skin inflammation. HDM extract not only increased IL-22Rα expression and TARC production in HaCaT but also enhanced IL-22, tumor necrosis factor (TNF)-α and interferon (IFN)-γ production in T cells. The HDM extract-induced IL-22 from T cells significantly increased the production of IL-1α, IL-6 and TARC in HaCaT cells. In addition, we found that TARC produced in HDM extract-treated HaCaT induced T-cell recruitment. These results suggest that there is a direct involvement of HDM extract-induced IL-22 in TARC production and T-cell migration. Taken together, TARC production in HaCaT through the interaction between IL-22 and IL-22Rα facilitates T-cell migration. These data show one of the reasons for inflammation in the skin lesions of AD patients.Entities:
Keywords: atopic dermatitis; house dust mite; interleukin-22; interleukin-22 receptor; thymus and activation regulated chemokine
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Year: 2016 PMID: 26914146 DOI: 10.1111/exd.12988
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960