Crosstalk between LXR and toll-like receptor signaling mediates bacterial and viral antagonism of cholesterol metabolism

Mol Cell. 2003 Oct;12(4):805-16. doi: 10.1016/s1097-2765(03)00384-8.

Abstract

The liver X receptors (LXR) alpha and beta are regulators of cholesterol metabolism and determinants of atherosclerosis susceptibility. Viral and bacterial pathogens have long been suspected to be modulators of atherogenesis; however, mechanisms linking innate immunity to cholesterol metabolism are poorly defined. We demonstrate here that pathogens interfere with macrophage cholesterol metabolism through inhibition of the LXR signaling pathway. Activation of Toll-like receptors (TLR) 3 and 4 by microbial ligands blocks the induction of LXR target genes including ABCA1 in cultured macrophages as well as in aortic tissue in vivo. As a consequence of these transcriptional effects, TLR3/4 ligands strongly inhibit cholesterol efflux from macrophages. Crosstalk between LXR and TLR signaling is mediated by IRF3, a specific effector of TLR3/4 that inhibits the transcriptional activity of LXR on its target promoters. These findings highlight a common mechanism whereby bacterial and viral pathogens may modulate macrophage cholesterol metabolism and cardiovascular disease.

Publication types

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

MeSH terms

  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters / biosynthesis
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, Differentiation / genetics
  • Arteriosclerosis / metabolism
  • Arteriosclerosis / virology
  • Bacterial Infections / metabolism*
  • Cell Line
  • Cholesterol / metabolism*
  • DNA-Binding Proteins / genetics
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / genetics
  • Genes, Regulator / genetics
  • Interferon Regulatory Factor-3
  • Ligands
  • Liver X Receptors
  • Macrophages / metabolism
  • Macrophages / virology
  • Membrane Glycoproteins / drug effects
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88
  • NF-kappa B / genetics
  • Orphan Nuclear Receptors
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / genetics
  • Receptors, Cell Surface / drug effects
  • Receptors, Cell Surface / metabolism*
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Receptors, Immunologic / genetics
  • Signal Transduction / physiology
  • Toll-Like Receptor 3
  • Toll-Like Receptors
  • Transcription Factors / genetics
  • Virus Diseases / metabolism*

Substances

  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters
  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • DNA-Binding Proteins
  • Interferon Regulatory Factor-3
  • Irf3 protein, mouse
  • Ligands
  • Liver X Receptors
  • Membrane Glycoproteins
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Nr1h3 protein, mouse
  • Orphan Nuclear Receptors
  • Receptors, Cell Surface
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Immunologic
  • Toll-Like Receptor 3
  • Toll-Like Receptors
  • Transcription Factors
  • Cholesterol