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Atherosclerosis in Transgenic Mice Overexpressing Apolipoprotein A-II

Authors: C H, Warden; C C, Hedrick; J H, Qiao; L W, Castellani; A J, Lusis;

Atherosclerosis in Transgenic Mice Overexpressing Apolipoprotein A-II

Abstract

Concentrations of plasma high density lipoprotein (HDL) are inversely correlated with atherosclerotic coronary artery disease. The two most abundant protein constituents of HDL are apolipoproteins A-I and A-II (apoA-I and apoA-II). ApoA-I is required for assembly of HDL and, when overexpressed in transgenic mice, confers resistance to early atherosclerosis. The present studies reveal that transgenic mice that overexpress mouse apoA-II had elevated HDL-cholesterol concentrations but, nevertheless, exhibited increased atherosclerotic lesion development as compared to normal mice. The HDL in the transgenic mice was larger and had an increased ratio of apoA-II to apoA-I. Thus, both the composition and amount of HDL appear to be important determinants of atherosclerosis.

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Keywords

Male, Apolipoprotein A-I, Arteriosclerosis, Mice, Transgenic, Mice, Inbred C57BL, Mice, Cholesterol, Mice, Inbred DBA, Animals, Female, Lipoproteins, HDL, Apolipoprotein A-II, Crosses, Genetic

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
354
Top 10%
Top 1%
Top 1%
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