Bile salt-stimulated phospholipid efflux mediated by ABCB4 localized in nonraft membranes

Abstract

ABCB4 is necessary for the secretion of phospholipids from hepatocytes into bile and for the protection of cell membranes against bile salts. Lipid rafts are plasma membrane microdomains containing high contents of cholesterol and sphingolipids, which are separated by Triton X-100 extraction or OptiPrep gradient centrifugation. In this study, we investigated the relationship between the function of ABCB4 and lipid rafts using mouse canalicular membranes and HEK293 cells stably expressing ABCB4. ABCB4 and ABCB1 were mainly distributed in nonraft membranes. The expression of ABCB4, but not ABCB1, led to significant increases in the phosphatidylcholine (PC), phosphatidylethanolamine (PE), and sphingomyelin (SM) contents in nonraft membranes and further enrichment of SM and cholesterol in raft membranes. The ABCB4-mediated effl ux of PC, PE, and SM was significantly stimulated by taurocholate, while the effl ux of PE and SM was much less than that of PC. This ABCB4-mediated effl ux was completely abolished by BODIPY -verapamil, which hardly partitioned into raft membranes. In addition, ABCB1 and ABCB4 mediated the effl ux of rhodamine 123 and rhodamine 6G from nonraft membranes, which was not affected by taurocholate. We conclude that ABCB4 located in nonrafts, but not in rafts, is predominantly involved in the effl ux of phospholipids and other substrates. Copyright © 2013 by the American Society for Biochemistry and Molecular Biology, Inc.