Increased type II transforming growth factor-beta receptor expression in liver cells during cholesterol challenge

Atherosclerosis. 2000 Sep;152(1):51-7. doi: 10.1016/s0021-9150(99)00449-9.

Abstract

A large body of evidences implicates transforming growth factor-beta (TGF-beta) in the pathogenesis of atherosclerosis. In this context, TGF-beta receptor dysfunction has been suggested to be relevant. We tested the effect of hypercholesterolemia, a well-known risk factor for atherosclerosis, on liver type II TGF-beta receptor (TbetaR-II) expression in atherosclerosis-susceptible C57BL/6 mouse strain fed atherogenic diet. In addition, the relationship between cholesterol and TbetaR-II expression was verified by cholesterol challenge on human hepatoma cell (HepG2) cultures. The susceptible C57BL/6 mice fed atherogenic diet exhibited significant mRNA and immunohistochemical TbetaR-II liver expression at 2, 5, 9 and 15 weeks as compared to animals fed a regular diet. The TbetaR-II profile on HepG2 resulted in a time-dependent increased expression when the cells were incubated with soluble free cholesterol, associated with an increased TGF-beta-dependent biological activity as detected by luciferase assay of reporter gene. These data provide evidence for a cholesterol-dependent TbetaR-II induction that may play a potentially relevant role in the development of hypercholesterolemia and atherogenesis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Arteriosclerosis / metabolism
  • Arteriosclerosis / pathology
  • Blotting, Northern
  • Blotting, Western
  • Cells, Cultured
  • Cholesterol / metabolism*
  • Diet, Atherogenic*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Immunohistochemistry
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • Probability
  • Receptors, Transforming Growth Factor beta / analysis*
  • Reference Values
  • Sensitivity and Specificity
  • Statistics, Nonparametric
  • Up-Regulation / physiology*

Substances

  • Receptors, Transforming Growth Factor beta
  • Cholesterol