To evaluate mechanisms that mediate passage of unconjugated bilirubin (UCB)
across placenta, the transport of [H-3]UCB was studied in the human tropho
blastic, BeWo cell line. When plotted against the unbound UCB concentration
[B-f], uptake exhibited saturative kinetics with a similar apparent K-m (s
imilar to 30 nM) for BeWo cells grown either in polarized (Transwell) or no
n-polarized fashion (dish), UCB release from cells, but not uptake, was inh
ibited by sulfobromophthalein but not by taurocholate, and almost abolished
by MK571, a specific inhibitor of the activity of multidrug resistance-ass
ociated proteins (MRPs). MRP1 and MRP5 were both present in BeWo cells and
the expression of MRP1, but not MRP5, was markedly higher in polarized cell
s. 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
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