ABCA12 regulates ABCA1-dependent cholesterol efflux from macrophages and the development of atherosclerosis
Details
Publication Year 2013-08-06,Volume 18,Issue #2,Page 225-38
Journal Title
Cell metabolism
Publication Type
Journal Article
Abstract
ABCA12 is involved in the transport of ceramides in skin, but it may play a wider role in lipid metabolism. We show that, in Abca12-deficient macrophages, cholesterol efflux failed to respond to activation with LXR agonists. Abca12 deficiency caused a reduction in the abundance of Abca1, Abcg1, and Lxrbeta. Overexpression of Lxrbeta reversed the effects. Mechanistically, Abca12 deficiency did not affect expression of genes involved in cholesterol metabolism. Instead, a physical association between Abca1, Abca12, and Lxrbeta proteins was established. Abca12 deficiency enhanced interaction between Abca1 and Lxrbeta and the degradation of Abca1. Overexpression of ABCA12 in HeLa-ABCA1 cells increased the abundance and stability of ABCA1. Abca12 deficiency caused an accumulation of cholesterol in macrophages and the formation of foam cells, impaired reverse cholesterol transport in vivo, and increased the development of atherosclerosis in irradiated Apoe(-/-) mice reconstituted with Apoe(-/-)Abca12(-/-) bone marrow. Thus, ABCA12 regulates the cellular cholesterol metabolism via an LXRbeta-dependent posttranscriptional mechanism.
Publisher
Elsevier
Keywords
ABCA12
Research Division(s)
Cancer And Haematology
NHMRC Grants
NHMRC/1016647
Terms of Use/Rights Notice
Copyright © 2013 Elsevier Inc. All rights reserved.


Creation Date: 2014-01-24 12:02:22
An error has occurred. This application may no longer respond until reloaded. Reload 🗙