Aberrant expression of claudin-4 and -7 in hepatocytes in the cirrhotic human liver

Med Mol Morphol. 2015 Mar;48(1):33-43. doi: 10.1007/s00795-014-0074-z. Epub 2014 Apr 16.

Abstract

The liver comprises hepatocytes and non-parenchymal cells such as bile duct epithelial cells. Claudin-4 and -7 are not expressed in hepatocytes under physiological conditions. It was reported that claudin-7 increased in human pulmonary fibroses. We therefore investigated claudin-4 and -7 expressions in human cirrhotic livers, in which hepatocyte proliferation is severely delayed. We examined liver tissues from 50 patients with liver tumors. The expression of claudin-4 and -7 in hepatocytes significantly increased with the grade of fibrosis, not with inflammatory activity, in the liver tissues of chronic hepatitis. The number of claudin-4- and -7-positive cells observed was greater than that of alpha-fetoprotein-positive hepatic progenitor cells. In primary cultures of mouse hepatocytes, the expression of claudin-4 and -7 was not induced by treatment with proinflammatory cytokines. In immunohistochemical analysis of liver tissues of 3,5-diethoxycarbonyl-1,4-dihydrocollidine-treated mice and primary cultures of mouse hepatocytes, the expression of claudin-4 and -7 increased with proliferation of progenitor cells. However, the claudin-4- and -7-positive cells were not always progenitor cells. Thus, claudin-4 and -7 were observed in hepatocytes of severely damaged mouse and human livers. These findings suggest that claudin-4- and -7-positive hepatocytes may exist during the process of differentiation from progenitor cells into mature hepatocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Claudin-4 / biosynthesis*
  • Claudins / biosynthesis*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Humans
  • Immunohistochemistry
  • Interleukin-1beta / pharmacology
  • Interleukin-6 / pharmacology
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Microscopy, Fluorescence
  • Oncostatin M / pharmacology
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • CLDN7 protein, human
  • Claudin-4
  • Claudins
  • Interleukin-1beta
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Oncostatin M