Decreased susceptibility to diet-induced atherosclerosis in human apolipoprotein A-II transgenic mice

Arterioscler Thromb Vasc Biol. 2000 Nov;20(11):2453-8. doi: 10.1161/01.atv.20.11.2453.

Abstract

Studies performed in vivo have been controversial regarding the implication of human apolipoprotein (apo)A-II in the atherogenic process. Expression of human apoA-II in transgenic mice fed a chow diet leads to (1) a bimodal distribution of high density lipoprotein (HDL) size as in humans, (2) a reduction in total cholesterol concentration that is mainly due to a reduction in non-HDL cholesterol level, and (3) a dramatic reduction in mouse endogenous apoA-I and apoA-II. After 20 weeks on an atherogenic diet, transgenic mice had reduced total cholesterol concentrations because of a reduction in cholesterol associated with all lipoprotein classes. Endogenous apoA-I and apoA-II were also dramatically decreased in transgenic mice. The mean area of atherosclerotic lesions was drastically decreased in transgenic mice (-44%, P=0.0027) compared with control mice. The amount of aortic surface covered by lesions was positively correlated with very low density lipoprotein cholesterol (P<0.01) and intermediate density lipoprotein cholesterol levels (P<0.05). Transgenic mice were protected against the development of atherosclerosis despite a marked decrease in HDL cholesterol and apoA-I concentrations. This protection may be related to the marked reduction in circulating low density lipoprotein (very low density and intermediate density lipoprotein) levels in transgenic mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Nutritional Physiological Phenomena
  • Animals
  • Apolipoprotein A-II / blood
  • Apolipoprotein A-II / genetics*
  • Apolipoproteins / blood
  • Arteriosclerosis / enzymology
  • Arteriosclerosis / genetics*
  • Arteriosclerosis / pathology
  • Arteriosclerosis / prevention & control*
  • Biological Transport / genetics
  • Cholesterol / metabolism
  • Cholesterol, HDL / blood
  • Cholesterol, HDL / chemistry
  • Diet, Atherogenic*
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Lipids / blood
  • Lipoprotein Lipase / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Phosphatidylcholine-Sterol O-Acyltransferase / metabolism
  • Serum Albumin

Substances

  • Apolipoprotein A-II
  • Apolipoproteins
  • Cholesterol, HDL
  • Lipids
  • Serum Albumin
  • Cholesterol
  • Phosphatidylcholine-Sterol O-Acyltransferase
  • Lipoprotein Lipase