Bile salts regulate proliferation and apoptosis of liver cells by modulating the IGF1 system

Dig Liver Dis. 2007 Jul;39(7):654-62. doi: 10.1016/j.dld.2007.03.008. Epub 2007 May 24.

Abstract

Background: In different cell types, the insulin-like growth factor 1 and its receptor modulate growth, apoptosis and damage repair in cooperation with estrogen receptors.

Aim: To evaluate the involvement of the insulin-like growth factor 1 system and estrogen receptors in bile salts modulation of apoptosis/proliferation of hepatocytes and cholangiocytes. Primary cultures of rat hepatocytes and cholangiocytes were exposed to glycochenodeoxycholate or tauro-CDC in the presence or absence of insulin-like growth factor 1 receptor blocking antibody (alphaIR3), small interfering RNA for insulin-like growth factor 1, 17beta-estradiol or estrogen receptor antagonist (ICI 182,780). Proliferation was evaluated by proliferating cell nuclear antigen Western blot and apoptosis by measuring caspase-3 activity or annexin-V.

Results: In hepatocytes, the insulin-like growth factor 1 receptor blocker enhanced glycochenodeoxycholate-induced apoptosis and caused tauro-CDC to promote apoptosis. 17Beta-estradiol or the estrogen receptor antagonist (ICI 182,780) did not influence the apoptotic effect of glycochenodeoxycholate. In cholangiocytes, both glycochenodeoxycholate and tauro-CDC induced proliferation at 100microM, while they induced apoptosis at 1mM with a more pronounced effect of glycochenodeoxycholate. Apoptosis induced by 1mM glycochenodeoxycholate or tauro-CDC in cholangiocytes was enhanced by blocking insulin-like growth factor 1 receptor or by silencing insulin-like growth factor 1. 17Beta-estradiol counteracts glycochenodeoxycholate-induced cholangiocyte apoptosis by enhancing insulin-like growth factor 1 secretion and activating the insulin-like growth factor 1 system.

Conclusions: Modulation of the IGF1 system could represent a potential strategy for the management of bile salts-induced liver injury.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Bile Acids and Salts / metabolism*
  • Bile Ducts / cytology
  • Bile Ducts / metabolism
  • Cell Proliferation*
  • Hepatocytes / metabolism
  • Hepatocytes / physiology*
  • Insulin-Like Growth Factor I / metabolism*
  • Male
  • Rats
  • Rats, Wistar
  • Receptor, IGF Type 1 / metabolism
  • Receptors, Estrogen / metabolism

Substances

  • Bile Acids and Salts
  • Receptors, Estrogen
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1