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Updated: May 30, 2026

Quantification of Atherosclerosis in Mice
Published on: June 12, 2019
Global functional knockdown of ATP binding cassette transporter A1 stimulates development of atherosclerosis in apoE
Nigora Mukhamedova1, Wilissa D'Souza, Hann Low
1Baker Heart and Diabetes Institute, Melbourne, Australia.
Abstract:
ABCA1 is a key element of cellular cholesterol homeostasis. ApoE K/O mice fed with high-fat diet were infused with anti-ABCA1 antibody or control IgM. Infusion of anti-ABCA1 antibody led to 72% increase in the area of atherosclerotic plaque in aorta. After 16 weeks on high-fat diet plasma level of high density lipoprotein cholesterol (HDL-C) was reduced in control group, but was unchanged in mice infused with anti-ABCA1 antibody. Total plasma cholesterol level was elevated while the capacity of plasma to support cholesterol efflux ex vivo was reduced after 16 weeks on high-fat diet; the effects were similar in the two groups. We conclude that functional blocking of ABCA1-dependent cholesterol efflux stimulates development of atherosclerosis in apoE K/O mice independently from HDL-C levels.
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