Department of Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, University of Tübingen, Wilhelmstr. 56, D-72074 Tübingen, Germany.
Biol Chem. 2010 Feb-Mar;391(2-3):139-148. doi: 10.1515/bc.2010.012.
The liver is the major organ for metabolism of drugs and other xenobiotics. Expression of many drug-metabolizing enzymes is not equally distributed throughout the liver: under normal conditions, many of them, including the most relevant members of the cytochrome P450 superfamily, are exclusively expressed in a hepatocyte subpopulation located near branches of the efferent central vein. Activation of different ligand-dependent transcription factors by exogenous compounds stimulates high expression of certain cytochrome P450 isoforms. This process also occurs preferentially in perivenous hepatocytes. The mechanisms, however, which determine the zone-specificity of basal and xenobiotic-induced expression of cytochrome P450 enzymes, have remained largely unknown for decades. Very recently, signaling through the Wnt/beta-catenin pathway has been implicated in the regulation of zonal gene expression in mouse liver. In this review, current knowledge of cytochrome P450 regulation by beta-catenin-dependent transcription is summarized and underlying molecular mechanisms are discussed.
肝脏是药物和其他外源物质代谢的主要器官。许多药物代谢酶的表达在肝脏中不是均匀分布的:在正常情况下,它们中的许多酶,包括细胞色素 P450 超家族中最重要的成员,仅在靠近流出中央静脉分支的肝实质细胞亚群中表达。外源性化合物通过激活不同的配体依赖性转录因子,刺激某些细胞色素 P450 同工酶的高表达。这个过程也优先发生在近中静脉的肝实质细胞中。然而,几十年来,决定细胞色素 P450 酶基础表达和外源诱导表达的区域特异性的机制在很大程度上仍然未知。最近,Wnt/β-连环蛋白信号通路在调节小鼠肝脏的区域基因表达方面的作用已被涉及。在这篇综述中,总结了β-连环蛋白依赖性转录对细胞色素 P450 调节的最新知识,并讨论了潜在的分子机制。