Deficiency of Adipose Differentiation-Related Protein Impairs Foam Cell Formation and Protects Against Atherosclerosis
- 20 June 2008
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 102 (12) , 1492-1501
- https://doi.org/10.1161/circresaha.107.168070
Abstract
Foam cells are a hallmark of atherosclerosis. However, it is unclear whether foam cell formation per se protects against atherosclerosis or fuels it. In this study, we investigated the role of adipose differentiation-related protein (ADFP), a major lipid droplet protein (LDP), in the regulation of foam cell formation and atherosclerosis. We show that ADFP expression facilitates foam cell formation induced by modified lipoproteins in mouse macrophages in vitro. We show further that Adfp gene inactivation in apolipoprotein E–deficient (ApoE−/−) mice reduces the number of lipid droplets in foam cells in atherosclerotic lesions and protects the mice against atherosclerosis. Moreover, transplantation of ADFP-null bone marrow-derived cells effectively attenuated atherosclerosis in ApoE−/− mice. Deficiency of ADFP did not cause a detectable compensatory increase in the other PAT domain proteins in macrophages in vitro or in vivo. Mechanistically, ADFP enables the macrophage to maintain its lipid content by hindering lipid efflux. We detected no significant difference in lesion composition or in multiple parameters of inflammation in macrophages or in their phagocytic activity between mice with and without ADFP. In conclusion, Adfp inactivation in ApoE−/− background protects against atherosclerosis and appears to be a relatively pure model of impaired foam cell formation.Keywords
This publication has 42 references indexed in Scilit:
- Macrophage-specific transgenic expression of cholesteryl ester hydrolase significantly reduces atherosclerosis and lesion necrosis in Ldlr–/– miceJournal of Clinical Investigation, 2007
- Phagocytosis in atherosclerosis: Molecular mechanisms and implications for plaque progression and stabilityCardiovascular Research, 2007
- Nosology of primary vasculitisCurrent Opinion in Rheumatology, 2007
- The inflammatory cytokine response of cholesterol-enriched macrophages is dampened by stimulated pinocytosisJournal of Leukocyte Biology, 2006
- Endothelial lipase modulates HDL but has no effect on atherosclerosis development in apoE−/− and LDLR−/− miceJournal of Lipid Research, 2005
- Genes of Cholesterol Metabolism in Human AtheromaArteriosclerosis, Thrombosis, and Vascular Biology, 2005
- Proteomic Analysis of Proteins Associated with Lipid Droplets of Basal and Lipolytically Stimulated 3T3-L1 AdipocytesJournal of Biological Chemistry, 2004
- The endoplasmic reticulum is the site of cholesterol-induced cytotoxicity in macrophagesNature Cell Biology, 2003
- Inflammation in atherosclerosisNature, 2002
- Purification, cloning, and expression of a human enzyme with acyl coenzyme A: cholesterol acyltransferase activity, which is identical to liver carboxylesterase.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1994