Epithelial-mesenchymal transitions of bile duct epithelial cells in primary hepatolithiasis

J Korean Med Sci. 2010 Jul;25(7):1066-70. doi: 10.3346/jkms.2010.25.7.1066. Epub 2010 Jun 17.

Abstract

The purpose of this study was to explore the role of epithelial-mesenchymal transition in the pathogenesis of hepatolithiasis. Thirty-one patients with primary hepatolithiasis were enrolled in this study. Expressions of E-cadherin, alpha-catenin, alpha-SMA, vimentin, S100A4, TGF-beta1 and P-smad2/3 in hepatolithiasis bile duct epithelial cells were examined by immunohistochemistry staining. The results showed that the expressions of the epithelial markers E-cadherin and alpha-catenin were frequently lost in hepatolithiasis (32.3% and 25.9% of cases, respectively), while the mesenchymal markers vimentin, alpha-SMA and S100A4 were found to be present in hepatolithiasis (35.5%, 29.0%, and 32.3% of cases, respectively). The increased mesenchymal marker expression was correlated with decreased epithelial marker expression. The expressions of TGF-beta1 and P-smad2/3 in hepatolithiasis were correlated with the expression of S100A4. These data indicate that TGF-beta1-mediated epithelial-mesenchymal transition might be involved in the formation of hepatolithiasis.

Keywords: Bile Duct Epithelial Cell; Epithelial-mesenchymal Transition; Immunohistochemistry; Primary Hepatolithiasis; Transforming Growth Factor beta1.

MeSH terms

  • Adult
  • Bile Ducts* / cytology
  • Bile Ducts* / metabolism
  • Bile Ducts* / pathology
  • Biomarkers / metabolism*
  • Cell Differentiation / physiology*
  • Epithelial Cells / cytology
  • Epithelial Cells / physiology*
  • Epithelium / physiology
  • Female
  • Gallstones* / metabolism
  • Gallstones* / pathology
  • Humans
  • Liver Diseases / metabolism
  • Liver Diseases / pathology*
  • Male
  • Mesoderm / cytology
  • Mesoderm / physiology*
  • Middle Aged

Substances

  • Biomarkers