Ductular morphogenesis and functional polarization of normal human biliary epithelial cells in three-dimensional culture

J Hepatol. 2001 Jul;35(1):2-9. doi: 10.1016/s0168-8278(01)00078-2.

Abstract

Background/aims: The understanding of the physiology and function of human biliary epithelial cells (hBEC) has been improved by studies in monolayer culture systems. The aim was to develop a polarized model to elucidate the mechanisms of ductular morphogenesis and functional differentiation of hBEC.

Methods: The morphological, phenotypic and functional properties of hBEC cultured as three-dimensional aggregates in collagen gel were assessed in medium supplemented with (or without) human hepatocyte growth factor (hHGF) and foetal bovine serum.

Results: In the absence of added mitogens and serum, cells maintained as morphologically polarized aggregates, organized around a central lumen, were positive for phenotypic markers of biliary epithelium and negative for markers of other cell types. Functional markers, gamma-glutamyl-transferase, anion exchanger-2, responses to gamma interferon and forskolin induced secretion, were preserved. hHGF increased both the size and number of aggregates and induced hBEC to invade the gel and lumena forming anastomosing networks of cells.

Conclusions: Collagen gel culture in the absence of added growth factors and serum provides a model for analysis of the polarized functions of hBEC. The formation of poorly organized cords of cells in response to hHGF suggests that collagen gel culture may provide a model for the investigation of atypical ductular morphogenesis of the human biliary tract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Bile Ducts / cytology
  • Bile Ducts / drug effects
  • Bile Ducts / growth & development*
  • Bile Ducts / physiology*
  • Cattle / blood
  • Cell Division / physiology
  • Cell Polarity / physiology*
  • Cells, Cultured
  • Coculture Techniques
  • Collagen
  • Cytological Techniques
  • Epithelial Cells / drug effects
  • Epithelial Cells / physiology
  • Fetal Blood
  • Gels
  • Hepatocyte Growth Factor / pharmacology
  • Hepatocytes / physiology
  • Humans
  • Phenotype
  • Reference Values

Substances

  • Gels
  • Hepatocyte Growth Factor
  • Collagen

Grants and funding