Influence of interferon-gamma on the extent and phenotype of diet-induced atherosclerosis in the LDLR-deficient mouse

Arterioscler Thromb Vasc Biol. 2003 Mar 1;23(3):454-60. doi: 10.1161/01.ATV.0000059419.11002.6E. Epub 2003 Jan 30.

Abstract

Objective: The aim of this study was to investigate the influence of interferon-gamma (IFN-gamma) on atherosclerosis in low density lipoprotein receptor (LDLR)-null mice.

Methods and results: We cross-bred IFN-gamma-deficient mice with LDLR-null mice and analyzed lipoprotein profiles and atherosclerosis in the compound mutant progeny after 8 and 20 weeks on a cholesterol-enriched diet. IFN-gamma deficiency did not affect serum cholesterol levels or lipoprotein profiles, but it did affect the extent and phenotype of atherosclerosis. Atherosclerotic lesions in IFN-gamma-deficient mice were reduced by 75% in the aortic arch and by 46% in the descending aorta compared with control mice after 8 weeks on the diet. After 20 weeks, arch lesions were reduced by 43%, and descending aorta lesions were reduced by 65% in IFN-gamma-deficient mice compared with controls. At 8 weeks, percent lesional macrophage and smooth muscle content was significantly less in the IFN-gamma-deficient mice, but not at 20 weeks. Although there were fewer class II major histocompatibility complex-positive cells in the lesions of IFN-gamma-deficient animals compared with controls, class II major histocompatibility complex expression on endothelial cells overlying lesions persisted in the absence of IFN-gamma.

Conclusions: These data provide direct evidence that IFN-gamma influences atherosclerosis development and phenotype in the LDLR-deficient mouse, independent of changes in blood lipoprotein profiles.

Publication types

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

MeSH terms

  • Animals
  • Arteriosclerosis / metabolism*
  • Arteriosclerosis / pathology
  • CD4 Lymphocyte Count
  • Cytokines / metabolism
  • Female
  • Interferon-gamma / metabolism*
  • Leukocyte Count
  • Lipoproteins / blood
  • Male
  • Mice
  • Mice, Mutant Strains
  • Phenotype
  • Receptors, LDL / deficiency*
  • T-Lymphocytes / metabolism

Substances

  • Cytokines
  • Lipoproteins
  • Receptors, LDL
  • Interferon-gamma