Biliary wound healing, ductular reactions, and IL-6/gp130 signaling in the development of liver disease

World J Gastroenterol. 2006 Jun 14;12(22):3512-22. doi: 10.3748/wjg.v12.i22.3512.

Abstract

Basic and translational wound healing research in the biliary tree lag significantly behind similar studies on the skin and gastrointestinal tract. This is at least partly attributable to lack of easy access to the biliary tract for study. But clinical relevance, more interest in biliary epithelial cell (BEC) pathophysiology, and widespread availability of BEC cultures are factors reversing this trend. In the extra-hepatic biliary tree, ineffectual wound healing, scarring and stricture development are pressing issues. In the smallest intra-hepatic bile ducts either impaired BEC proliferation or an exuberant response can contribute to liver disease. Chronic inflammation and persistent wound healing reactions in large and small bile ducts often lead to liver cancer. General concepts of wound healing as they apply to the biliary tract, importance of cellular processes dependent on IL-6/gp130/STAT3 signaling pathways, unanswered questions, and future directions are discussed.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Bile Ducts / pathology
  • Bile Ducts / physiopathology*
  • Bile Ducts, Extrahepatic / pathology
  • Bile Ducts, Extrahepatic / physiopathology
  • Bile Ducts, Intrahepatic / pathology
  • Bile Ducts, Intrahepatic / physiopathology
  • Biliary Tract / pathology
  • Biliary Tract / physiopathology
  • Biliary Tract Diseases / pathology
  • Biliary Tract Diseases / physiopathology*
  • Cell Proliferation
  • Cytokine Receptor gp130 / physiology*
  • Epithelium / pathology
  • Epithelium / physiopathology
  • Humans
  • Inflammation
  • Interleukin-6 / physiology*
  • Liver Diseases / physiopathology*
  • STAT3 Transcription Factor / physiology
  • Signal Transduction / physiology*
  • Wound Healing / physiology*

Substances

  • Interleukin-6
  • STAT3 Transcription Factor
  • Cytokine Receptor gp130