Increased Cholesterol Efflux in Apolipoprotein AI (ApoAI)–Producing Macrophages as a Mechanism for Reduced Atherosclerosis in ApoAI (−/−) Mice

• DOI: 10.1161/hq1101.097798
• Publication Date: 2007-09-28T18:27:24Z
• Authors: Amy S. Major; Dwayne E. Dove; Hiroyuki Ishiguro; Yan Ru Su; Abigail M. Brown; Lily Liu; Kathy J. Carter; MacRae F. Linton; Sergio Fazio
• Keywords: Mice, Knockout; 0301 basic medicine; Apolipoprotein A-I; Arteriosclerosis; Macrophages; Biological Transport; Mice, Transgenic; Mice, Inbred C57BL; Mice; 03 medical and health sciences; Cholesterol; Macrophages, Peritoneal; Animals; Diet, Atherogenic; Humans; Lipoproteins, HDL; Cells, Cultured; Foam Cells

The concentration of apolipoprotein (apo) AI in the artery wall is thought to enhance cellular cholesterol efflux and protect against atherosclerosis. It has been shown that although macrophages do not make apoAI, they respond to it by increased cholesterol efflux. We hypothesized that macrophage production of apoAI would increase cholesterol efflux and reduce atherogenesis. In this study, we produced mice expressing human apoAI under the control of the macrophage-specific scavenger receptor-A promoter (mφ-AI). Human apoAI was detectable in the serum HDL fraction of mφ-AI transgenic mice at concentrations too low to affect serum cholesterol or HDL levels. Immunoblotting showed the presence of human apoAI in transgenic macrophage culture supernatants, mostly as lipoprotein-free protein, with a small component associated with HDL-like particles. Atherosclerosis studies using apoAI (−/−) mice transplanted with mφ-AI bone marrow showed that in the absence of macrophage-derived apoE, local expression of apoAI reduced diet-induced lesions in the proximal aorta. Additionally, mφ-AI macrophages showed a 40% increase in cholesterol efflux compared with control macrophages. These data support the hypothesis that apoAI production by macrophages in the artery wall is protective against atherosclerosis. This protection is likely mediated by increased cholesterol efflux and decreased foam cell formation in vivo.