Visualization and isolation of zone-specific murine hepatocytes that maintain distinct cytochrome P450 oxidase expression in primary culture

Biochem Biophys Res Commun. 2020 Jul 30;528(3):420-425. doi: 10.1016/j.bbrc.2020.05.202. Epub 2020 Jun 3.

Abstract

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.

Keywords: Cytochrome P450 oxidase; Drug metabolism; Metabolic zonation; Oxygen concentration; Primary hepatocytes; Wnt/β-catenin signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / toxicity
  • Animals
  • Cell Separation
  • Cells, Cultured
  • Flow Cytometry
  • Gene Expression
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hepatocytes / cytology
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Liver / anatomy & histology
  • Liver / cytology
  • Liver / metabolism
  • Mice
  • Mice, Transgenic
  • Mitochondria, Liver / metabolism
  • NADPH-Ferrihemoprotein Reductase / genetics
  • NADPH-Ferrihemoprotein Reductase / metabolism*
  • Oxygen / metabolism
  • Wnt Signaling Pathway / drug effects

Substances

  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Acetaminophen
  • NADPH-Ferrihemoprotein Reductase
  • Oxygen