Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver

Cell Mol Gastroenterol Hepatol. 2021;12(2):745-767. doi: 10.1016/j.jcmgh.2021.04.003. Epub 2021 Apr 15.

Abstract

Background & aims: Tight junctions in the liver are essential to maintain the blood-biliary barrier, however, the functional contribution of individual tight junction proteins to barrier and metabolic homeostasis remains largely unexplored. Here, we describe the cell type-specific expression of tight junction genes in the murine liver, and explore the regulation and functional importance of the transmembrane protein claudin-3 in liver metabolism, barrier function, and cell proliferation.

Methods: The cell type-specific expression of hepatic tight junction genes is described using our mouse liver single-cell sequencing data set. Differential gene expression in Cldn3-/- and Cldn3+/+ livers was assessed in young and aged mice by RNA sequencing (RNA-seq), and hepatic tissue was analyzed for lipid content and bile acid composition. A surgical model of partial hepatectomy was used to induce liver cell proliferation.

Results: Claudin-3 is a highly expressed tight junction protein found in the liver and is expressed predominantly in hepatocytes and cholangiocytes. The histology of Cldn3-/- livers showed no overt phenotype, and the canalicular tight junctions appeared intact. Nevertheless, by RNA-seq we detected a down-regulation of metabolic pathways in the livers of Cldn3-/- young and aged mice, as well as a decrease in lipid content and a weakened biliary barrier for primary bile acids, such as taurocholic acid, taurochenodeoxycholic acid, and taurine-conjugated muricholic acid. Coinciding with defects in the biliary barrier and lower lipid metabolism, there was a diminished hepatocyte proliferative response in Cldn3-/- mice after partial hepatectomy.

Conclusions: Our data show that, in the liver, claudin-3 is necessary to maintain metabolic homeostasis, retention of bile acids, and optimal hepatocyte proliferation during liver regeneration. The RNA-seq data set can be accessed at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE159914.

Keywords: Bile Acid; Claudin; Liver Regeneration; Single-Cell RNA Sequencing; Tight Junction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Animals
  • Bile Ducts / metabolism*
  • Cell Proliferation / genetics
  • Claudin-3 / deficiency*
  • Claudin-3 / metabolism
  • Gene Deletion
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Hepatectomy
  • Hepatocytes / metabolism
  • Lipid Metabolism / genetics
  • Liver / metabolism*
  • Liver / pathology*
  • Liver / ultrastructure
  • Liver Regeneration
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Tight Junctions / genetics
  • Tight Junctions / metabolism

Substances

  • Claudin-3