Institute for Clinical Chemistry and Laboratory Medicine, University of Regensburg, Germany.
J Photochem Photobiol B. 2012 Nov 5;116:79-88. doi: 10.1016/j.jphotobiol.2012.06.007. Epub 2012 Jun 25.
Many ATP binding cassette (ABC) transporters are important regulators of lipid homeostasis and have been implicated in keratinocyte lipid transport. Ultraviolet (UV) light exposure is a known epidermal stressor, which amongst other effects causes lipid alterations and defective lamellar body biogenesis. To elucidate the background of these lipid changes we studied the effect of UVB light on ABC transporter expression. The effect of UVB treatment on the levels of 47 known human ABC transporter mRNAs was analyzed in normal human epidermal keratinocytes. Immunoblots and promoter assays were carried out for ABCA1 and ABCG1. The mRNA levels of cholesterol transport regulators ABCA1 and ABCG1 were markedly downregulated by UVB, parallel to the lamellar ichthyosis related glucosylceramide transporter ABCA12 and the suspected sphingosine-1-phosphate and cholesterol sulfate transporter ABCC1. The long but not the short alternative splice variant of the ABCF2 was found to be markedly upregulated rapidly after UVB irradiation. Immunoblot confirmed ABCA1 and ABCG1 protein downregulation, and luciferase assays showed suppression of their promoters by UVB. These proteins mostly transport lipids, which account for the integrity of the epidermal barrier; therefore our findings on the UVB regulation of ABC transporters may explain the appearance of barrier dysfunction after UVB exposure.
许多 ATP 结合盒(ABC)转运蛋白是脂质动态平衡的重要调节剂,并且与角质形成细胞脂质转运有关。紫外线(UV)照射是一种已知的表皮应激源,除其他作用外,还会引起脂质改变和板层小体生物发生缺陷。为了阐明这些脂质变化的背景,我们研究了 UVB 光对 ABC 转运蛋白表达的影响。在正常的人表皮角质形成细胞中分析了 UVB 处理对 47 种已知人类 ABC 转运蛋白 mRNA 水平的影响。进行了 ABCA1 和 ABCG1 的免疫印迹和启动子测定。胆固醇转运调节剂 ABCA1 和 ABCG1 的 mRNA 水平明显下调,与板层状鱼鳞病相关的葡萄糖神经酰胺转运体 ABCA12 和疑似鞘氨醇-1-磷酸和胆固醇硫酸盐转运体 ABCC1 平行。发现 ABCF2 的长而非短的选择性剪接变体在 UVB 照射后迅速显著上调。免疫印迹证实 ABCA1 和 ABCG1 蛋白下调,并通过 UVB 显示其启动子受到抑制。这些蛋白主要运输脂质,脂质是表皮屏障完整性的基础;因此,我们关于 ABC 转运蛋白的 UVB 调节的发现可能解释了 UVB 暴露后屏障功能障碍的出现。