Süle Norbert, Tészás Alexandra, Kálmán Endre, Szigeti Réka, Miseta Attila, Kellermayer Richard
Department of Pathology, University of Pécs, Pécs, Hungary.
Pathol Oncol Res. 2006;12(4):234-6. doi: 10.1007/BF02893419. Epub 2006 Dec 25.
Autosomal dominant mutations in the genes encoding the calcium ATPases SERCA2 and PMRI/SPCA1 cause the genodermatoses Darier disease (DD) and Hailey-Hailey disease (HHD), respectively. Recent observations indicated that the level of the pathogenic proteins greatly decreases in the affected areas of the epidermis in these disorders. Here we addressed how lithium, a recognized exacerbating factor in Darier disease, affects the epidermal expression of SERCA2 and PMR1/SPCA1 in the rat as a model. Standard histologic and immunohistochemical methods were utilized in 3 lithium-treated and 3 control animals. A significant suppression of epidermal SERCA2 and PMR1 levels were observed as a result of lithium therapy in addition to marked qualitative and quantitative changes in the stratum corneum and the granular layer of the epidermis in the treated animals. Our findings suggest that exacerbating factors in calcium ATPase disorders of the skin suppress epidermal SERCA2 and PMR1 levels, further decreasing the already haploinsufficient protein expression to a potentially critical level in Darier disease and Hailey-Hailey disease, respectively. Lithium therapy should specifically be avoided not only in Darier disease, but Hailey-Hailey disease as well.
编码钙ATP酶SERCA2和PMR1/SPCA1的基因发生常染色体显性突变,分别导致遗传性皮肤病达里埃病(DD)和黑利-黑利病(HHD)。最近的观察表明,在这些疾病中,致病蛋白的水平在表皮的受影响区域大幅下降。在此,我们以大鼠为模型,研究了达里埃病中一种公认的加重因素锂如何影响SERCA2和PMR1/SPCA1在表皮中的表达。对3只锂处理大鼠和3只对照大鼠采用标准组织学和免疫组织化学方法。锂治疗导致表皮SERCA2和PMR1水平显著降低,同时处理组大鼠的角质层和表皮颗粒层出现明显的质和量的变化。我们的研究结果表明,皮肤钙ATP酶疾病中的加重因素会抑制表皮SERCA2和PMR1水平,进而分别将达里埃病和黑利-黑利病中本已单倍体不足的蛋白表达进一步降低到潜在的临界水平。不仅在达里埃病中,而且在黑利-黑利病中,都应特别避免使用锂治疗。