Kristl Jernej, Slanc Petra, Krasna Metka, Berlec Ales, Jeras Matjaz, Strukelj Borut
Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Askerceva 7, 1000, Ljubljana, Slovenia.
Pharm Res. 2008 Mar;25(3):521-9. doi: 10.1007/s11095-007-9388-z. Epub 2007 Aug 2.
Calcipotriol is a potent drug for topical treatment of psoriasis because it manages to inhibit keratinocyte proliferation. In the present study we investigated the effects of calcipotriol on gene expression in human keratinocytes in terms of mechanism of how calcipotriol decreases proliferation.
Cell proliferation was analyzed by MTT assay. The differential display approach together with qPCR was used to assess the gene expression after treatment. In addition, Western immunoblotting revealed differences on the protein level. Finally, transfection of the KCs with specific small interfering RNA determined the genes necessary to inhibit proliferation.
KCs proliferation was decreased in a concentration-dependent manner. Moreover, calcipotriol dowregulated the expression of two proliferation factors: early growth response-1 (EGR1) and polo-like kinase-2 (PLK2). The protein levels of EGR1 and PLK2 were also decreased. Specific siRNA against EGR1 and PLK2 in KCs resulted in marked reduction of EGR1 and PLK2 expression. In both cases, the reduction resolved in the decreased proliferation of KCs.
This study provides a new insight into how calcipotriol affects proliferation of keratinocytes by decreasing the expression of EGR1 and PLK2. Furthermore, the results offer groundwork for developing novel compounds for the treatment of hyperproliferative skin disorders like psoriasis.
卡泊三醇是一种用于银屑病局部治疗的强效药物,因为它能够抑制角质形成细胞增殖。在本研究中,我们从卡泊三醇降低增殖的机制方面研究了卡泊三醇对人角质形成细胞基因表达的影响。
通过MTT法分析细胞增殖。采用差异显示法结合qPCR评估处理后的基因表达。此外,蛋白质免疫印迹法揭示了蛋白质水平的差异。最后,用特异性小干扰RNA转染角质形成细胞,确定抑制增殖所需的基因。
角质形成细胞的增殖呈浓度依赖性降低。此外,卡泊三醇下调了两种增殖因子的表达:早期生长反应因子-1(EGR1)和波罗样激酶-2(PLK2)。EGR1和PLK2的蛋白质水平也降低。角质形成细胞中针对EGR1和PLK2的特异性siRNA导致EGR1和PLK2表达明显降低。在这两种情况下,这种降低都导致角质形成细胞增殖减少。
本研究为卡泊三醇如何通过降低EGR1和PLK2的表达影响角质形成细胞增殖提供了新的见解。此外,这些结果为开发用于治疗银屑病等过度增殖性皮肤病的新型化合物奠定了基础。