Interleukin-1: A key inflammatory mediator in psoriasis?

被引:64
作者
Mee, JB
Cork, MJ
di Giovine, FS
Duff, GW
Groves, RW
机构
[1] Univ London Kings Coll, St Thomas Hosp, St Johns Inst Dermatol, London SE1 7EH, England
[2] Univ Sheffield, Div Genom, Sheffield S10 2TN, S Yorkshire, England
关键词
IL-1; keratinocyte; psoriasis;
D O I
10.1016/j.cyto.2005.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pro-inflammatory cytokine interleukin-1 (IL-1) is constitutively expressed by keratinocytes in vivo and has been shown to be expressed in psoriatic lesional skin. To determine what role the IL-1 system might contribute to the inflammatory process in psoriasis, semi-quantitative RT-PCR and cRNA microarray studies were performed on biopsies excised from lesional and non-lesional skin. Whilst IL-1 alpha mRNA levels showed a reduction in lesional skin in a subset of patients, steady state IL-1 beta mRNA was increased markedly. Neither of the two IL-1 receptor transcripts nor total IL-1 receptor antagonist exhibited major changes within the lesion. Expression of the IL-1-induced chemokine IL-8 was only observed in lesional epidermis. Functional genomic experiments comparing transcriptome profiles derived from psoriatic lesional skin and IL-1 stimulated keratinocytes demonstrated a striking level of overlap. Taken together, these data suggest that IL-1 is likely to be an important mediator in the initiation and maintenance of psoriatic plaques and may represent an attractive therapeutic target. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:72 / 78
页数:7
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