A review of the physiological and immunological functions of biliary epithelial cells: targets for primary biliary cirrhosis, primary sclerosing cholangitis and drug-induced ductopenias

Clin Dev Immunol. 2004 Sep-Dec;11(3-4):205-13. doi: 10.1080/17402520400004177.

Abstract

Our understanding of biliary epithelial cells (BEC) in physiobiology and immunology has steadily expanded. BEC transports IgA as well as IgM into bile, synthesizes and secretes various chemokines, cytokines, and expresses adhesion molecules involved in cell interaction and signal transduction. These then suggest a myriad of potential roles for BEC in defense from invading microorganisms as well as the pathogenesis of diverse immunologically driven diseases such as primary biliary cirrhosis (PBC), graft-versus-host disease, and primary sclerosing cholangitis (PSC). Despite the progress, there still remain many areas of BEC biology that require further investigation. Most importantly, it remains to be clarified that the extent to which the immunologic activities observed in BEC represent a BEC response to tissue injury or whether BEC themselves are the active participants in the pathogenesis of various cholestatic immunological diseases, including PBC and PSC.

Publication types

  • Review

MeSH terms

  • Bile / physiology
  • Bile Ducts / drug effects
  • Bile Ducts / pathology
  • Biliary Tract / cytology
  • Biliary Tract / immunology*
  • Biliary Tract / physiology*
  • Cell Adhesion Molecules / metabolism
  • Chemokines / biosynthesis
  • Cholangitis, Sclerosing / etiology*
  • Cholangitis, Sclerosing / immunology
  • Cholangitis, Sclerosing / physiopathology
  • Cytokines / biosynthesis
  • Electrolytes / metabolism
  • Epithelial Cells / immunology
  • Epithelial Cells / physiology
  • Humans
  • Immunoglobulin A, Secretory / physiology
  • Ion Transport
  • Liver Cirrhosis, Biliary / etiology*
  • Liver Cirrhosis, Biliary / immunology
  • Liver Cirrhosis, Biliary / physiopathology
  • Models, Biological

Substances

  • Cell Adhesion Molecules
  • Chemokines
  • Cytokines
  • Electrolytes
  • Immunoglobulin A, Secretory