School of Clinical Dentistry, University of Sheffield, Sheffield, UK.
MRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
Exp Dermatol. 2018 May;27(5):473-475. doi: 10.1111/exd.13483. Epub 2018 Jan 5.
CYP3A4 and CYP4A5 share specificity for a wide range of xenobiotics with the CYP3 subfamily collectively involved in the biotransformation of approximately 30% of all drugs. CYP3A4/5 mRNA transcripts have been reported in the skin, yet knowledge of their protein expression and function is lacking. In this study, we observed gene and protein expression of CYP3A4/5 in both human skin and tissue-engineered skin equivalents (TESEs), and enzyme activity was detected using the model substrate benzyl-O-methyl-cyanocoumarin. Mass spectrometric analysis of TESE lysates following testosterone application revealed a time-dependent increase in metabolite production, confirming the functional expression of these enzymes in skin.
CYP3A4 和 CYP4A5 与 CYP3 亚家族一起对广泛的外源物质具有特异性,共同参与约 30%的所有药物的生物转化。CYP3A4/5 mRNA 转录物已在皮肤中报道,但对其蛋白表达和功能知之甚少。在这项研究中,我们观察到 CYP3A4/5 在人皮肤和组织工程皮肤等效物 (TESE) 中的基因和蛋白表达,并使用模型底物苯甲氧基甲基-氰基香豆素检测酶活性。应用睾酮后对 TESE 裂解物进行质谱分析显示代谢产物产生呈时间依赖性增加,证实这些酶在皮肤中的功能表达。