Oxysterol-induced up-regulation of MCP-1 expression and synthesis in macrophage cells

Free Radic Biol Med. 2005 Nov 1;39(9):1152-61. doi: 10.1016/j.freeradbiomed.2005.06.024. Epub 2005 Aug 11.


To investigate the proinflammatory potential of cholesterol and cholesterol oxidation products (oxysterols), which are present in oxidized low-density lipoproteins, foam cells, and fibrotic plaque, we used an in vitro model mimicking the challenge of macrophage cells by the cholesterol accumulating within the central core of atheroma. A biologically representative oxysterol mixture was shown to be potentially able to sustain a chronic inflammatory process within the vascular wall by up-regulating the expression of defined proinflammatory genes. In particular, expression and synthesis of the major chemokine for monocytes/macrophages, namely monocyte chemotactic protein-1 (MCP-1), were consistently increased when cells of the macrophage lineage (U937 cell line) were incubated with this mixture. On the contrary, an identical concentration of unoxidized cholesterol in no case modified expression or synthesis of the chemokine. Up-regulated expression and synthesis of MCP-1 by the oxysterol mixture was clearly dependent on a net increment of phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) and nuclear factor kappaB (NF-kappaB) nuclear binding. The results indicate that cholesterol may contribute to the progression of atherosclerotic lesions by strongly up-regulating crucial proinflammatory factors like MCP-1, but only after having been oxidized to oxysterols.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Cell Line
  • Chemokine CCL2 / biosynthesis*
  • Chemokine CCL2 / genetics
  • Cholesterol / metabolism*
  • Cholesterol / pharmacology
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Gene Expression
  • Humans
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • NF-kappa B / metabolism
  • Oxidation-Reduction
  • Phosphorylation
  • Up-Regulation


  • CCL2 protein, human
  • Chemokine CCL2
  • NF-kappa B
  • Cholesterol
  • Extracellular Signal-Regulated MAP Kinases