The LPS2 mutation in TRIF is atheroprotective in hyperlipidemic low density lipoprotein receptor knockout mice

Innate Immun. 2013 Feb;19(1):20-9. doi: 10.1177/1753425912447130. Epub 2012 May 25.

Abstract

Signaling through MyD88, an adaptor utilized by all TLRs except TLR3, is pro-atherogenic; however, it is unknown whether signaling through TIR-domain-containing adaptor-inducing interferon-β (TRIF), an adaptor used only by TLRs 3 and 4, is relevant to atherosclerosis. We determined that the TRIF(Lps2) lack-of-function mutation was atheroprotective in hyperlipidemic low density lipoprotein (LDL) receptor knockout (LDLr(-/-)) mice. LDLr(-/-) mice were crossed with either TRIF(Lps2) or TLR3 knockout mice. After feeding an atherogenic diet for 10-15 wks, atherosclerotic lesions in the heart sinus and aorta were quantitated. LDLr(-/-) mice with TRIF(Lps2) were significantly protected from atherosclerosis. TRIF(Lps2) led to a reduction in cytokines secreted from peritoneal macrophages (M) in response to hyperlipidemia. Moreover, heart sinus valves from hyperlipidemic LDLr(-/-) TRIF(Lps2) mice had significantly fewer lesional M. However, LDLr(-/-) mice deficient in TLR3 showed some enhancement of disease. Collectively, these data suggest that hyperlipidemia resulting in endogenous activation of the TRIF signaling pathway from TLR4 leads to pro-atherogenic events.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Adaptor Proteins, Vesicular Transport / metabolism*
  • Animals
  • Aorta / pathology
  • Atherosclerosis / etiology
  • Atherosclerosis / genetics*
  • Atherosclerosis / pathology
  • Atherosclerosis / prevention & control
  • Coronary Vessels / pathology
  • Cytokines / immunology
  • Diet, Atherogenic
  • Hyperlipidemias / complications
  • Hyperlipidemias / genetics*
  • Hyperlipidemias / pathology
  • Lipoproteins, LDL / genetics
  • Lipoproteins, LDL / metabolism*
  • Macrophages, Peritoneal / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Mutant Strains
  • Mutation / genetics
  • Myeloid Differentiation Factor 88 / metabolism
  • Signal Transduction / genetics
  • Toll-Like Receptor 3 / genetics
  • Toll-Like Receptor 3 / metabolism*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Cytokines
  • Lipoproteins, LDL
  • Myeloid Differentiation Factor 88
  • TICAM-1 protein, mouse
  • TLR3 protein, human
  • Toll-Like Receptor 3