作者: Tatsuo KANDA , Laurent FOUCAND , Yuichi NAKAMURA , Isabelle NIOT , Philippe BESNARD
DOI: 10.1042/BJ3300261
关键词: Bile acid 、 CYP8B1 、 Fatty acid-binding protein 、 CYP27A1 、 Biochemistry 、 Biology 、 Cholestyramine 、 G protein-coupled bile acid receptor 、 Chenodeoxycholic acid 、 Deoxycholic acid
摘要: Molecular mechanisms of the bile acid active transport system in ileal enterocytes remain unknown. We examined whether acids affect human enterocyte gene expression intestinal acid-binding protein (I-BABP), a component this system. Differentiated Caco-2 cells were incubated presence bile, or other lipids. The level I-BABP was evaluated by Northern and Western blot analyses. A 24 h incubation medium containing either resulted remarkable 7.5-fold increase mRNA over control level. Neither cholesterol, palmitic acid, phosphatidylcholine nor cholestyramine treated showed any difference from control. Bile treatment increased time- dose-dependent manner. analysis that induction led to cytosolic I-BABP. Chenodeoxycholic deoxycholic greater effects than hydrophilic acids, including their own glycine conjugates. Pretreatment actinomycin D cycloheximide completely inhibited up-regulation acid. especially lipophilic Caco-2-cells, suggesting luminal play an important role regulating expression.