期刊
FEBS LETTERS
卷 495, 期 1-2, 页码 94-99出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/S0014-5793(01)02357-2
关键词
placenta; expression; fetus; multidrug resistance-associated protein; bilirubin; transport
To evaluate mechanisms that mediate passage of unconjugated bilirubin (UCB) across placenta, the transport of [H-3]UCB was studied in the human trophoblastic, BeWo cell line. When plotted against the unbound UCB concentration [B-f], uptake exhibited saturative kinetics with a similar apparent K-m (similar to 30 nM) for BeWo cells grown either in polarized (Transwell) or non-polarized fashion (dish), UCB release from cells, but not uptake, was inhibited by sulfobromophthalein but not by taurocholate, and almost abolished by MK571, a specific inhibitor of the activity of multidrug resistance-associated proteins (MRPs). MRP1 and MRP5 were both present in BeWo cells and the expression of MRP1, but not MRP5, was markedly higher in polarized cells. These data indicate that UCB is taken up from the fetal circulation by a still undefined, saturative process not shared by other organic anions and is then excreted to maternal circulation by proteins of the MRP family. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据