Kennedy Matthew A, Barrera Gabriel C, Nakamura Kotoka, Baldán Angel, Tarr Paul, Fishbein Michael C, Frank Joy, Francone Omar L, Edwards Peter A
Department of Biological Chemistry, CHS 33-257, David Geffen School of Medicine, University of California Los Angeles, 10833 Le Conte Avenue, Los Angeles, California 90095, USA.
Cell Metab. 2005 Feb;1(2):121-31. doi: 10.1016/j.cmet.2005.01.002.
Here we demonstrate that the ABC transporter ABCG1 plays a critical role in lipid homeostasis by controlling both tissue lipid levels and the efflux of cellular cholesterol to HDL. Targeted disruption of Abcg1 in mice has no effect on plasma lipids but results in massive accumulation of both neutral lipids and phospholipids in hepatocytes and in macrophages within multiple tissues following administration of a high-fat and -cholesterol diet. In contrast, overexpression of human ABCG1 protects murine tissues from dietary fat-induced lipid accumulation. Finally, we show that cholesterol efflux to HDL specifically requires ABCG1, whereas efflux to apoA1 requires ABCA1. These studies identify Abcg1 as a key gene involved in both cholesterol efflux to HDL and in tissue lipid homeostasis.
在此我们证明,ABC转运蛋白ABCG1通过控制组织脂质水平以及细胞胆固醇向高密度脂蛋白(HDL)的流出,在脂质稳态中发挥关键作用。在小鼠中靶向破坏Abcg1对血浆脂质没有影响,但在给予高脂高胆固醇饮食后,会导致多个组织中的肝细胞和巨噬细胞内中性脂质和磷脂大量积累。相比之下,人ABCG1的过表达可保护小鼠组织免受饮食脂肪诱导的脂质积累。最后,我们表明胆固醇向HDL的流出特别需要ABCG1,而向载脂蛋白A1(apoA1)的流出需要ABCA1。这些研究确定Abcg1是参与胆固醇向HDL流出以及组织脂质稳态的关键基因。