Tachibana Shizuko, Hirano Maki, Hirata Takashi, Matsuo Michinori, Ikeda Ikuo, Ueda Kazumitsu, Sato Ryuichiro
Department of Applied Biological Chemistry, Graduate School of Agriculture and Life Sciences, University of Tokyo, Tokyo, Japan.
Biosci Biotechnol Biochem. 2007 Aug;71(8):1886-95. doi: 10.1271/bbb.70109. Epub 2007 Aug 7.
In this study we analyzed functions of ATP-binding cassette (ABC) transporters involved in sterol transport from Caco-2 cells. Treatment with a synthetic liver x receptor ligand elevated both mRNA and protein levels of ABCG5, G8, and ABCA1. The ligand stimulated cholesterol efflux, suggesting that ABC transporters are involved in it. To identify the acceptors of cholesterol, potential molecules such as apolipoprotein A-I, glycocholic acid, phosphatidylcholine, and bile acid micelles were added to the medium. Apo A-I, a known acceptor of cholesterol transported by ABCA1, elevated cholesterol efflux on the basal side, whereas the others raised cholesterol efflux on the apical side. Moreover, bile acid micelles preferentially augmented plant sterol efflux rather than cholesterol. Finally, in HEK293 cells stably expressing ABCG5/G8, bile acid micelle-mediated sterol efflux was significantly accelerated. These results indicate that ABCG5/G8, unlike ABCA1, together with bile acids should participate in sterol efflux on the apical surface of Caco-2 cells.
在本研究中,我们分析了参与从Caco-2细胞转运固醇的ATP结合盒(ABC)转运蛋白的功能。用合成肝X受体配体处理可提高ABCG5、G8和ABCA1的mRNA和蛋白质水平。该配体刺激胆固醇流出,表明ABC转运蛋白参与其中。为了鉴定胆固醇的受体,向培养基中添加了诸如载脂蛋白A-I、甘氨胆酸、磷脂酰胆碱和胆汁酸微团等潜在分子。载脂蛋白A-I是ABCA1转运的已知胆固醇受体,可提高基底侧的胆固醇流出,而其他分子则提高顶端侧的胆固醇流出。此外,胆汁酸微团优先增加植物固醇流出而非胆固醇流出。最后,在稳定表达ABCG5/G8的HEK293细胞中,胆汁酸微团介导的固醇流出显著加速。这些结果表明,与ABCA1不同,ABCG5/G8应与胆汁酸一起参与Caco-2细胞顶端表面的固醇流出。