Center for Matrix Biology and Medicine, Graduate School of Medicine, Tokai University, Isehara, Japan; Department of Innovative Medical Science, Tokai University School of Medicine, Isehara, Japan.
Department of Preventive Medicine, Tokai University School of Medicine, Isehara, Japan.
Biochem Biophys Res Commun. 2020 Jul 30;528(3):420-425. doi: 10.1016/j.bbrc.2020.05.202. Epub 2020 Jun 3.
Parenchymal hepatocytes are responsible for most of the metabolic functions of the liver, but exhibit distinct functional properties depending on their localization within the hepatic lobule. Cytochrome P450 oxidases represent a family of drug-metabolizing enzymes, which are expressed predominantly in hepatocytes localized in the centrilobular area (zone 3). The present study describes a unique transgenic mouse strain that distinguishes zone 3 hepatocytes from periportal zone 1 hepatocytes by the intensity of EGFP fluorescence. Both zone 1 and zone 3 hepatocytes isolated from these mice showed the same zone-specific gene expression patterns as in liver tissue in vivo. Experiments using primary cultures of hepatocytes indicated that a combination of low oxygen concentration and activation of Wnt/β-catenin signaling maintained the expression of zone 3-specific P450 drug-metabolizing enzymes, which was characterized by their susceptibility to acetaminophen-induced mitochondrial dysfunction. These zone-specific hepatocytes provide a useful system in the research area of liver pathophysiology and drug development.
实质肝细胞负责肝脏的大部分代谢功能,但根据其在肝小叶内的定位表现出明显的功能特性。细胞色素 P450 氧化酶代表一组药物代谢酶,主要表达在位于中央小叶区(区 3)的肝细胞中。本研究描述了一种独特的转基因小鼠品系,通过 EGFP 荧光强度将区 3 肝细胞与门周区 1 肝细胞区分开来。从这些小鼠中分离的区 1 和区 3 肝细胞均表现出与体内肝组织相同的区特异性基因表达模式。使用原代肝细胞培养物进行的实验表明,低氧浓度和 Wnt/β-连环蛋白信号激活的组合维持了区 3 特异性 P450 药物代谢酶的表达,其特征是对乙酰氨基酚诱导的线粒体功能障碍敏感。这些区特异性肝细胞为肝脏病理生理学和药物开发的研究领域提供了一个有用的系统。