Pikuleva Irina A
Department of Pharmacology and Toxicology, University of Texas, Medical Branch, 301 University Blvd., Galveston, TX 77555-1031, USA.
Drug Metab Dispos. 2006 Apr;34(4):513-20. doi: 10.1124/dmd.105.008789. Epub 2006 Jan 24.
By catalyzing the first steps in different pathways of cholesterol degradation, cytochromes P450 (P450s) 7A1, 27A1, 11A1, and 46A1 play key roles in cholesterol homeostasis. CYP7A1 is a microsomal liver-specific enzyme that converts cholesterol to 7alpha-hydroxycholesterol. CYP27A1 is a ubiquitously expressed mitochondrial P450 that metabolizes cholesterol to 27-hydroxycholesterol. CYP11A1 also resides in mitochondria but is expressed mainly in steroidogenic tissues, where it catalyzes the conversion of cholesterol to pregnenolone. Finally, CYP46A1 is a brain-selective microsomal monooxygenase producing 24S-hydroxycholesterol from cholesterol. Catalytic efficiencies of cholesterol-metabolizing P450s vary significantly and probably reflect physiological requirements of different organs for the rate of cholesterol turnover. P450s 7A1, 27A1, 11A1, and 46A1 represent a unique system for elucidation of how different enzymes have adapted to fit their specific roles in cholesterol elimination. Studies of cholesterol-metabolizing P450s suggest that their activities could be modulated post-translationally and that they should also be considered as targets for regulation of cholesterol homeostasis.
细胞色素P450(P450s)7A1、27A1、11A1和46A1通过催化胆固醇降解不同途径中的起始步骤,在胆固醇稳态中发挥关键作用。CYP7A1是一种微粒体肝脏特异性酶,可将胆固醇转化为7α-羟基胆固醇。CYP27A1是一种广泛表达的线粒体P450,可将胆固醇代谢为27-羟基胆固醇。CYP11A1也存在于线粒体中,但主要在类固醇生成组织中表达,在那里它催化胆固醇转化为孕烯醇酮。最后,CYP46A1是一种脑选择性微粒体单加氧酶,可将胆固醇转化为24S-羟基胆固醇。胆固醇代谢P450s的催化效率差异很大,可能反映了不同器官对胆固醇周转速率的生理需求。P450s 7A1、27A1、11A1和46A1代表了一个独特的系统,用于阐明不同的酶如何适应其在胆固醇消除中的特定作用。对胆固醇代谢P450s的研究表明,它们的活性可以在翻译后进行调节,并且它们也应被视为调节胆固醇稳态的靶点。