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Title 

Corticotropin-releasing hormone (CRH) downregulates interleukin-18 expression in human HaCaT keratinocytes by activation of p38 mitogen-activated protein kinase (MAPK) pathway

Authors 

H J ParkH J KimJ H LeeJ Y LeeB K ChoJ S KangH KangYoung YangD H Cho

Publisher 

Nature Publishing Group

Issue Date 

2005

Citation 

Journal of Investigative Dermatology, vol. 124, no. 4, pp. 751-755

Keywords 

corticotropin-releasing hormone (CRH)interleukin 18 (IL-18)p38 mitogen-activated protein kinase (p38 MARK)corticotropin releasing factorinterleukin 1interleukin 10interleukin 12interleukin 18interleukin 2interleukin 4

Abstract 

It is generally accepted that corticotropin-releasing hormone (CRH) acts as the main coordinator of the central response to stress. Stress or an abnormal response to stressors has been found to modify the evolution of skin disorders, including psoriasis and atopic dermatitis. Nevertheless, the specific pathogenic role of stress remains unknown in skin diseases. Interleukin (IL)-18, a member of the IL-1 family, is a key mediator of peripheral inflammation and host defense responses, and is secreted by human keratinocytes. Here, we investigated the regulatory effect of CRH on expression of IL-18 in skin keratinocytes. Exposure of HaCaT cells to CRH resulted in a reduction of IL-18 mRNA transcripts and its production was in a concentration-dependent manner. In order to investigate whether the mitogen-activated protein kinase (MAPK) signaling pathway is involved in the downregulation of IL-18 production, cells were pre-treated with SB203580, an inhibitor of p38 MAPK, prior to the addition of CRH. This pretreatment blocked the decrease in IL-18 production. In addition, CRH treatment induced rapid phosphorylation of p38 MAPK. SB203580 were able to inhibit CRH-induced p38 MAPK phosphorylation. CRH also inhibited production of IL-18 in human primary keratinocytes. These results suggest that CRH regulates IL-18 production through the MAPK signaling pathway in human keratinocytes.

ISSN 

0022-202X

Link 

http://dx.doi.org/10.1111/j.0022-202X.2005.23656.x

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2017-04-19


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