Regulation of caspase 14 expression in keratinocytes by inflammatory cytokines - a possible link between reduced skin barrier function and inflammation?

被引:68
|
作者
Hvid, Malene [1 ,2 ]
Johansen, Claus [1 ]
Deleuran, Bent [2 ,3 ]
Kemp, Kaare [4 ]
Deleuran, Mette [1 ]
Vestergaard, Christian [1 ]
机构
[1] Aarhus Univ Hosp, Dept Dermatovenereol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Inst Med Microbiol & Immunol, Aarhus C, Denmark
[3] Aarhus Univ Hosp, Dept Rheumatol, DK-8000 Aarhus C, Denmark
[4] Leo Pharma, Ballerup, Denmark
关键词
caspase; 14; filaggrin; keratinocytes; skin barrier function; skin inflammation; ATOPIC-DERMATITIS; PSORIATIC EPIDERMIS; FILAGGRIN; DIFFERENTIATION;
D O I
10.1111/j.1600-0625.2011.01280.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Caspase 14 is a unique member of the cysteinyl aspartate-specific proteinase family. Its expression is confined primarily to cornified epithelium such as the skin. Caspase 14 has been associated with the processing of filaggrin monomers and the development of natural moisturising factors of the skin, and thus, it could be speculated that caspase 14 dysregulation is implicated in the development of an impaired skin barrier function. We have investigated the regulation of caspase 14 transcription in cultured primary keratinocytes following stimulation with a number of factors present in inflamed skin, including T(H)1- and T(H)2-Associated cytokines in addition to LPS and peptidoglycan. In particular, we found that T(H)2-associated cytokines reduced the caspase 14 mRNA level significantly. Furthermore, we found that the expression of caspase 14 was reduced in skin biopsies from patients with atopic dermatitis (AD), psoriasis and contact dermatitis, further supporting a role for this kinase in inflammatory skin conditions. Hence, the regulation of caspase 14 levels provides a possible link between impaired skin barrier function and inflammatory reactions in skin diseases such as AD and may offer an explanation to the skin barrier dysfunction in inflamed skin lesions.
引用
收藏
页码:633 / 636
页数:4
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