Eliminating atherogenesis in mice by switching off hepatic lipoprotein secretion

Article

关键词: E-DEFICIENT MOUSE;    EXCLUSIVELY APOLIPOPROTEIN B48;    TRIGLYCERIDE TRANSFER PROTEIN;    DENSITY-LIPOPROTEIN;    KNOCKOUT MICE;    GENE-EXPRESSION;    ATHEROSCLEROSIS;    RECEPTOR;    MODEL;    B100;   

DOI  :  10.1161/01.CIR.0000054781.50889.0C

来源: SCIE

【 摘 要 】

Background-LDL receptor-deficient apolipoprotein (apo)-B100-only mice (Ldlr(-/-)Apob(100/100) have elevated LDL cholesterol levels on a chow diet and develop severe aortic atherosclerosis. We hypothesized that both the hypercholesterolemia and the susceptibility to atherosclerosis could be eliminated by switching off hepatic lipoprotein production. Methods and Results-We bred Ldlr(-/-)Apob(100/100) mice that were homozygous for a conditional allele for Mttp (the gene for microsomal triglyceride transfer protein) and the inducible Mx1-Cre transgene. In these animals, which we called Reversa mice, the hypercholesterolemia could be reversed, without modifying the diet or initiating a hypolipidemic drug, by the transient induction of Cre expression in the liver. After Cre induction, hepatic Mttp expression was virtually eliminated (as judged by quantitative real-time PCR), hepatic lipoprotein secretion was abolished (as judged by electron microscopy), and LDLs were virtually eliminated from the plasma. Intestinal lipoprotein production was unaffected. In mice fed a chow diet, Cre induction reduced plasma cholesterol levels from 233.9+/-46.0 to 37.2+/-6.5 mg/dL. In mice fed a high-fat diet, cholesterol levels fell from 525.7+/-32.2 to 100.6+/-14.3 mg/dL. The elimination of hepatic lipoprotein production completely prevented both the development of atherosclerosis and the changes in gene expression that accompany atherogenesis. Conclusions-We developed mice in which hypercholesterolemia can be reversed with a genetic switch. These mice will be useful for understanding gene-expression changes that accompany the reversal of hypercholesterolemia and atherosclerosis.

【 授权许可】

Free