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Cholesterol biosynthesis from lanosterol: development of a novel assay method and characterization of rat liver microsomal lanosterol delta 24-reductase.

机译:羊毛甾醇的胆固醇生物合成:一种新型测定方法的开发和大鼠肝脏微粒体羊毛甾醇δ24-还原酶的表征。

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摘要

The membrane-bound sterol delta 24-reductase (24-reductase) catalyses anaerobic reduction of the 24(25)-enes of lanosterol and other obligatory intermediates of cholesterol biosynthesis from lanosterol. A novel assay method and properties of the 24-reductase are described. More than a 120-fold induction of the 24-reductase activity was achieved by feeding rats a diet containing 5% cholestyramine plus 0.1% lovastatin in chow and by modulating diurnal variation. With this enzyme induction condition, lanosterol was converted efficiently into dihydrolanosterol in both intact hepatic microsomes and freshly isolated hepatocytes only when either miconazole or CO was added to inhibit 14 alpha-demethylation of lanosterol. AR45 cells, which are deficient in 14 alpha-methyl demethylase (14 alpha-DM), exhibit lanosterol 24-reductase activity without addition of either CO or miconazole. Conversely, inhibition of the 24-reductase was not required for the expression of 14 alpha-DM activity. Studies on the substrate specificities for the 24-reductase using different 24(25)-enes showed that the most reactive substrate was 5 alpha-cholesta-7,24-dien-3 beta-ol, which exhibited a maximal 18-fold higher kcat than that of lanosterol without the aid of the 14 alpha-DM inhibitor. In addition, both the kinetic behaviour of lanosterol substrate in relation to the 24-reductase and a non-competitive inhibition mode of U18666A (Ki 0. 157 microM) as well as Triparanol (Ki 0.523 microM), two well-known 24-reductase inhibitors, were determined. On the basis of our new findings on the preferred substrate and on the negative effect of 14 alpha-DM on the 24-reductase, we suggest that C-24 reduction of sterols takes place straight after sterol delta 8-->7 isomerization of zymosterol, which occurs several steps after C-32 demethylation of lanosterol in the 19-step pathway of cholesterol biosynthesis from lanosterol.
机译:膜结合固醇三角洲24还原酶(24-还原酶)催化厌氧还原羊毛甾醇的24(25)-烯和从羊毛甾醇合成胆固醇的其他强制性中间体。描述了一种新颖的测定方法和24-还原酶的性质。通过给大鼠喂食含5%胆甾醇胺加0.1%洛伐他汀的饮食并调节昼夜变化,可实现24-还原酶活性的120倍以上诱导。在这种酶诱导条件下,仅当添加咪康唑或CO抑制羊毛脂的14α-脱甲基化时,羊毛脂才能在完整的肝微粒体和新鲜分离的肝细胞中有效地转化为二氢羊毛甾醇。缺乏14α-甲基脱甲基酶(14 alpha-DM)的AR45细胞在不添加CO或咪康唑的情况下表现出羊毛甾醇24-还原酶活性。相反,表达14α-DM活性不需要抑制24-还原酶。使用不同的24(25)-烯对24-还原酶的底物特异性的研究表明,反应性最强的底物是5 alpha-cholesta-7,24-dien-3 beta-ol,其最大kcat高18倍。不含14α-DM抑制剂的羊毛脂。此外,羊毛甾醇底物相对于24-还原酶的动力学行为和U18666A(Ki 0. 157 microM)的非竞争性抑制模式以及Triparanol(Ki 0.523 microM)是两种众所周知的24-还原酶确定了抑制剂。根据我们在优选底物上的新发现以及14 alpha-DM对24-还原酶的负面影响,我们建议在甾醇δ8- 7莫甾醇的异构化之后,立即发生C-24固醇的还原,这发生在羊毛脂的C-32脱甲基之后的19步中,是从羊毛甾醇进行胆固醇生物合成的几个步骤。

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