Takahashi H, Oyama N, Itoh Y, Ishida-Yamamoto A, Kaneko F, Iizuka H
Department of Dermatology, Asahikawa Medical College, Asahikawa, 078-8510, Japan.
Biochem Biophys Res Commun. 2000 Nov 30;278(3):719-23. doi: 10.1006/bbrc.2000.3850.
The transcriptional activator protein-2 (AP-2) has been suggested to participate in keratinocyte gene regulation. Cystatin A, a cysteine proteinase inhibitor, is one of the cornified cell envelope constituents and is expressed in the upper epidermis. We report AP-2-dependent transcriptional regulation of cystatin A gene expression of keratinocytes. At least three isoforms of AP-2 (AP-2 alpha, beta, gamma) have been described. Transfection of AP-2alpha, beta and gamma expression vectors into cultured normal human keratinocytes (NHK) resulted in increased cystatin A expression in both mRNA and protein levels. Among the three isoforms AP-2gamma was most potent in inducing cystatin A expression. In contrast, transfection of antisense oriented AP-2gamma expression vector decreased basal AP-2 expression, accompanied by decreased cystatin A mRNA. The fragment, +77 to -478 of 5'-flanking region of human cystatin A gene, was subcloned into chloramphenicol acetyltransferase (CAT) reporter vector (p478CAT). Cotransfection of p478CAT vector with AP-2alpha, beta, and gamma expression vectors resulted in three-, three-, and sixfold increase in the CAT activity, respectively. Transfection of the deleted construct (p478DeltaAP-2CAT, devoid of AP-2-like binding site (-75 to -84)) decreased CAT activity by one-third compared to p478CAT promoter activity. Cotransfection of p478DeltaAP-2CAT with AP-2alpha, beta, and gamma expression vectors had no effect on the decreased promoter activity. Immunohistochemical analysis of human skin showed that AP-2alpha is exclusively expressed in the nuclei of basal cell layer. AP-2gamma is expressed in the nuclei of basal, spinous, and granular cell layers. AP-2beta expression was not observed in the epidermis. Gel mobility shift assay revealed that the AP-2gamma protein specifically binds to oligonucleotides containing AP-2-like binding site of cystatin A gene. These results indicate that AP-2gamma regulates the cystatin A gene expression of epidermal keratinocytes at the transcriptional level.
转录激活蛋白 -2(AP -2)已被认为参与角质形成细胞的基因调控。胱抑素A是一种半胱氨酸蛋白酶抑制剂,是角质化细胞包膜成分之一,在上层表皮中表达。我们报告了角质形成细胞中胱抑素A基因表达的AP -2依赖性转录调控。已描述了至少三种AP -2同工型(AP -2α、β、γ)。将AP -2α、β和γ表达载体转染到培养的正常人角质形成细胞(NHK)中,导致胱抑素A在mRNA和蛋白质水平上的表达增加。在这三种同工型中,AP -2γ在诱导胱抑素A表达方面最有效。相反,转染反义方向的AP -2γ表达载体降低了基础AP -2的表达,同时胱抑素A mRNA也减少。将人胱抑素A基因5'侧翼区的 +77至 -478片段亚克隆到氯霉素乙酰转移酶(CAT)报告载体(p478CAT)中。将p478CAT载体与AP -2α、β和γ表达载体共转染,分别导致CAT活性增加了三倍、三倍和六倍。与p478CAT启动子活性相比,转染缺失构建体(p478DeltaAP -2CAT,缺乏AP -2样结合位点(-75至 -84))使CAT活性降低了三分之一。将p478DeltaAP -2CAT与AP -2α、β和γ表达载体共转染对降低的启动子活性没有影响。对人皮肤的免疫组织化学分析表明,AP -2α仅在基底细胞层的细胞核中表达。AP -2γ在基底、棘状和颗粒细胞层的细胞核中表达。在表皮中未观察到AP -2β的表达。凝胶迁移率变动分析表明,AP -2γ蛋白特异性结合含有胱抑素A基因AP -2样结合位点的寡核苷酸。这些结果表明,AP -