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25-羟维生素 D-24-羟化酶(CYP24A1):其在维生素 D 降解中的重要作用。

25-Hydroxyvitamin D-24-hydroxylase (CYP24A1): its important role in the degradation of vitamin D.

机构信息

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON, Canada K7L 3N6.

出版信息

Arch Biochem Biophys. 2012 Jul 1;523(1):9-18. doi: 10.1016/j.abb.2011.11.003. Epub 2011 Nov 12.

Abstract

CYP24A1 is the cytochrome P450 component of the 25-hydroxyvitamin D(3)-24-hydroxylase enzyme that catalyzes the conversion of 25-hydroxyvitamin D(3) (25-OH-D(3)) and 1,25-dihydroxyvitamin D(3) (1,25-(OH)(2)D(3)) into 24-hydroxylated products, which constitute the degradation of the vitamin D molecule. This review focuses on recent data in the CYP24A1 field, including biochemical, physiological and clinical developments. Notable among these are: the first crystal structure for rat CYP24A1; mutagenesis studies which change the regioselectivity of the enzyme; and the finding that natural inactivating mutations of CYP24A1 cause the genetic disease idiopathic infantile hypercalcemia (IIH). The review also discusses the emerging correlation between rising serum phosphate/FGF-23 levels and increased CYP24A1 expression in chronic kidney disease, which in turn underlies accelerated degradation of both serum 25-OH-D(3) and 1,25-(OH)(2)D(3) in this condition. This review concludes by evaluating the potential clinical utility of blocking this enzyme with CYP24A1 inhibitors in various disease states.

摘要

CYP24A1 是细胞色素 P450 家族的一员,也是 25-羟维生素 D(3)-24-羟化酶的组成部分,能够催化 25-羟维生素 D(3)(25-OH-D(3))和 1,25-二羟维生素 D(3)(1,25-(OH)(2)D(3))向 24-羟化产物的转化,这一过程构成了维生素 D 分子的降解。本综述重点介绍 CYP24A1 领域的最新数据,包括生化、生理和临床方面的进展。其中值得注意的是:首次获得了大鼠 CYP24A1 的晶体结构;酶的突变研究改变了酶的区域选择性;以及发现 CYP24A1 的天然失活突变会导致特发性婴儿高钙血症(IIH)这一遗传性疾病。本综述还讨论了在慢性肾脏病中,血清磷酸盐/FGF-23 水平升高与 CYP24A1 表达增加之间的新关联,这反过来又导致了该疾病状态下血清 25-OH-D(3)和 1,25-(OH)(2)D(3)的降解加速。最后,本综述通过评估在各种疾病状态下使用 CYP24A1 抑制剂来抑制这种酶的潜在临床应用价值。

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