School of Dietetics and Human Nutrition, McGill University, Ste Anne de Bellevue, QC, Canada.
Int J Biochem Cell Biol. 2013 Jul;45(7):1389-98. doi: 10.1016/j.biocel.2013.04.012. Epub 2013 Apr 17.
Bile acids have emerged as important biological molecules that support the solubilization of various lipids and lipid-soluble compounds in the gut, and the regulation of gene expression and cellular function. Bile acids are synthesized from cholesterol in the liver and eventually released into the small intestine. The majority of bile acids are recovered in the distal end of the small intestine and then returned to the liver for reuse. The components of the mechanism responsible for the recycling of bile acids within the enterohepatic circulation have been identified whereas the mechanism for intracellular transport is less understood. Recently, the ileal lipid binding protein (ILBP; human gene symbol FABP6) was shown to be needed for the efficient transport of bile acids from the apical side to the basolateral side of enterocytes in the distal intestine. This review presents an overview of the transport of bile acids between the liver and the gut as well as within hepatocytes and enterocytes. A variety of pathologies is associated with the malfunction of the bile acid transport system.
胆汁酸已成为支持肠道中各种脂质和脂溶性化合物溶解的重要生物分子,并且调节基因表达和细胞功能。胆汁酸是在肝脏中从胆固醇合成的,最终被释放到小肠中。大多数胆汁酸在小肠的远端被回收,然后被回收到肝脏中再利用。负责肠肝循环中胆汁酸再循环的机制的组成部分已经被确定,而细胞内运输的机制则不太清楚。最近,回肠脂质结合蛋白(ILBP;人基因符号 FABP6)被证明是从顶端到肠细胞的基底外侧有效地运输胆汁酸所必需的。这篇综述介绍了肝脏和肠道之间以及肝细胞和肠细胞内胆汁酸的运输概况。各种病理与胆汁酸转运系统的功能障碍有关。