Resveratrol increases the expression and activity of the low density lipoprotein receptor in hepatocytes by the proteolytic activation of the sterol regulatory element-binding proteins

Atherosclerosis. 2012 Feb;220(2):369-74. doi: 10.1016/j.atherosclerosis.2011.11.006. Epub 2011 Nov 16.

Abstract

Objective: The hepatocyte low density lipoprotein receptor (LDLR) plays a pivotal role in lipoprotein metabolism by lowering plasma LDL-cholesterol, a risk factor for atherosclerosis. The present study was conducted to investigate the effects of grape polyphenols on LDLR gene expression in human hepatocyte models.

Methods and results: Among the 14 phenolic compounds in red wine, we found that a stilbene trans-resveratrol most strongly up-regulated LDLR gene expression in HepG2 cells. Trans-resveratrol increased the LDLR protein and uptake of fluorescent-labeled LDL. Moreover, it enhanced LDLR gene promoter activity through the proteolytic activation of the sterol regulatory element-binding protein-2 (SREBP-2) as well as SREBP-1. However, sterols completely abolished trans-resveratrol-induced SREBP activation and LDLR gene expression. Finally, AMP-activated protein kinase (AMPK) knockdown analyses by siRNA revealed that AMPK activation was unnecessary for the effects of trans-resveratrol.

Conclusions: Trans-resveratrol up-regulated hepatic LDLR expression via proteolytic activation of SREBPs. We concluded that trans-resveratrol exhibits the anti-atherogenic effect, at least in part, by increased hepatic LDLR expression and subsequent LDL uptake.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Biological Transport
  • Dose-Response Relationship, Drug
  • Hep G2 Cells
  • Hepatocytes / drug effects*
  • Hepatocytes / enzymology
  • Humans
  • Lipoproteins, LDL / metabolism
  • Peptide Hydrolases / metabolism*
  • Promoter Regions, Genetic / drug effects
  • RNA Interference
  • RNA, Messenger / metabolism
  • Receptors, LDL / drug effects*
  • Receptors, LDL / genetics
  • Receptors, LDL / metabolism
  • Resveratrol
  • Sterol Regulatory Element Binding Protein 1 / metabolism*
  • Sterol Regulatory Element Binding Protein 2 / metabolism*
  • Stilbenes / pharmacology*
  • Time Factors
  • Transcriptional Activation / drug effects
  • Transfection
  • Up-Regulation

Substances

  • Lipoproteins, LDL
  • RNA, Messenger
  • Receptors, LDL
  • SREBF1 protein, human
  • SREBF2 protein, human
  • Sterol Regulatory Element Binding Protein 1
  • Sterol Regulatory Element Binding Protein 2
  • Stilbenes
  • AMP-Activated Protein Kinases
  • Peptide Hydrolases
  • Resveratrol