27-hydroxycholesterol induces production of tumor necrosis factor-alpha from macrophages

Biochem Biophys Res Commun. 2013 Jan 11;430(2):454-9. doi: 10.1016/j.bbrc.2012.12.021. Epub 2012 Dec 13.

Abstract

Enhanced production of TNF-α from macrophages promotes development and instability of atherosclerotic plaques, but involvement of lipid component in TNF-α production has not been clarified in atherosclerosis. We attempted to determine whether cholesterol oxidation products (oxysterols) could modify TNF-α production. Treatment of THP-1 cells with 27-hydroxycholesterol (27OHChol) or 7α-hydroxycholesterol (7αOHChol) resulted in a profound increase in TNF-α transcription, while treatment with an identical concentration of cholesterol and 7-ketochoelsterol did not lead to any change in TNF-α expression. Treatment with 27OHChol resulted in increased synthesis, as well as secretion, of TNF-α, while 7αOHChol led to increased synthesis of TNF-α without affecting secretion of the cytokine. Co-treatment with 7αOHChol or 27OHChol and LPS resulted in synergistically enhanced or augmented secretion of TNF-α. Treatment with TO-901317, pertussis toxin, PP2, and LY294002 resulted not only in attenuated transcription of TNF-α induced by 27OHChol and 7αOHChol, but also secretion of TNF-α enhanced by 27OHChol. This is the first report demonstrating enhanced production of TNF-α in macrophages by treatment with oxysterols which are detected in abundance in atheromatous lesions; in addition, results of the current study provide evidence indicating that certain types of oxysterols contribute to development of atherosclerosis by promoting production of proinflammatory cytokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chromones / pharmacology
  • Hydrocarbons, Fluorinated / pharmacology
  • Hydroxycholesterols / metabolism*
  • Hydroxycholesterols / pharmacology
  • Liver X Receptors
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Morpholines / pharmacology
  • Orphan Nuclear Receptors / agonists
  • Pertussis Toxin / pharmacology
  • Plaque, Atherosclerotic / metabolism*
  • Pyrimidines / pharmacology
  • Sulfonamides / pharmacology
  • Transcription, Genetic / drug effects
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / biosynthesis*
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • AG 1879
  • Chromones
  • Hydrocarbons, Fluorinated
  • Hydroxycholesterols
  • Liver X Receptors
  • Morpholines
  • Orphan Nuclear Receptors
  • Pyrimidines
  • Sulfonamides
  • T0901317
  • Tumor Necrosis Factor-alpha
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • 27-hydroxycholesterol
  • Pertussis Toxin