Increased nuclear β-catenin in suprabasal involved psoriatic epidermis

被引:35
作者
Hampton, P. J. [1 ]
Ross, O. K. [1 ]
Reynolds, N. J. [1 ]
机构
[1] Med Sch Newcastle Upon Tyne, Inst Cellular Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
adherens junctions; glycogen synthase kinase 3 beta; glycogen synthase kinase binding protein; keratinocyte; transglutaminase; 1;
D O I
10.1111/j.1365-2133.2007.08195.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Psoriasis is a common inflammatory skin disease characterized by abnormal keratinocyte proliferation and differentiation, increased angiogenesis and inflammation. There is evidence that some keratinocyte differentiation events are controlled by changes in cell-cell adhesion. beta-catenin is a 94-kDa protein which has a dual function as a component of intercellular adherens junctions and also as a transcription factor as part of the Wnt signalling pathway. beta-catenin is not required for keratinocyte proliferation but has been shown to regulate keratinocyte stem cells and hair follicle morphogenesis. To investigate the distribution and function of beta-catenin in involved psoriatic epidermis and in epidermal keratinocytes. Biopsies were obtained from patients with psoriasis and from normal controls. The distribution of beta-catenin was investigated using antibodies to both total and unphosphorylated active beta-catenin. Luciferase assays were used to measure transcriptional activation of transglutaminase 1 (TGase 1) and involucrin and to investigate the functional role of beta-catenin in interfollicular keratinocytes. Increased nuclear beta-catenin was seen in lesional suprabasal psoriatic epidermis compared with uninvolved or normal skin. Increased active unphosphorylated beta-catenin was also detected within the differentiating compartment of involved psoriatic epidermis. Expression of TGase 1 overlapped with beta-catenin in suprabasal lesional psoriasis. The TGase 1 promoter was positively regulated by activated beta-catenin and by the glycogen synthase kinase binding protein, suggesting that beta-catenin and glycogen synthase kinase 3 beta may regulate TGase 1 expression. This is the first report to convincingly demonstrate increased beta-catenin in involved psoriasis and to implicate beta-catenin in the regulation of TGase 1. This evidence suggests a role for beta-catenin signalling in regulating keratinocyte differentiation in interfollicular skin in addition to previously reported functions in stem cell fate determination, hair follicle regulation and skin tumorigenesis.
引用
收藏
页码:1168 / 1177
页数:10
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