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Diet-induced hypercholesterolemia and atherosclerosis in heterozygous apolipoprotein E-deficient mice.

Apolipoprotein (apo) E is a ligand for the receptor-mediated uptake of lipoprotein remnant particles. Complete absence of apo E in humans leads to a severe form of type III hyperlipoproteinemia. We have used targeted inactivation in murine embryonic stem cells, as also described by others, to specifically study the effects of heterozygous Apoe gene loss on the development of hyperlipidemia. After 6 weeks on a severe semi-synthetic atherogenic diet, heterozygous null mutants, with only one functional Apoe alle, developed hypercholesterolemia as compared with controls (10.1 mM vs. 4.7 mM serum cholesterol). Interestingly, serum cholesterol levels in female heterozygotes were doubled as compared with male heterozygotes (15.0 mM vs. 7.5 mM). On this diet, heterozygous apo E deficient mice also showed an increased susceptibility to atherosclerosis, depending on gender (mean lesion area per section of 9524 microns 2 vs. 61,388 microns 2 for males and females, respectively), whereas wild-type mice displayed far fewer lesions (354 microns 2 and 9196 microns 2 for males and females, respectively). This study indicates that a subnormal expression-level of the Apoe gene leads to hypercholesterolemia and, consequently, to an increased susceptibility to the development of atherosclerosis.

Pubmed ID: 7840811


  • van Ree JH
  • van den Broek WJ
  • Dahlmans VE
  • Groot PH
  • Vidgeon-Hart M
  • Frants RR
  • Wieringa B
  • Havekes LM
  • Hofker MH



Publication Data

November 2, 1994

Associated Grants


Mesh Terms

  • Aging
  • Animals
  • Apolipoproteins E
  • Arteriosclerosis
  • Blotting, Northern
  • Blotting, Western
  • Cholesterol
  • Cholesterol, Dietary
  • Diet, Atherogenic
  • Disease Susceptibility
  • Female
  • Gene Targeting
  • Heterozygote
  • Hypercholesterolemia
  • Lipids
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains