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Mechanisms for the transport of unconjugated bilirubin in human trophoblastic BeWo cells
Author(s) -
Pascolo Lorella,
Fernetti Cristina,
Garcia-Mediavilla Maria Victoria,
Ostrow J.Donald,
Tiribelli Claudio
Publication year - 2001
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(01)02357-2
Subject(s) - sulfobromophthalein , multidrug resistance associated protein 2 , chemistry , cell culture , abcg2 , bilirubin , fetus , placenta , atp binding cassette transporter , trophoblast , transporter , multidrug resistance associated proteins , biochemistry , endocrinology , medicine , biology , pregnancy , genetics , gene , liver function tests
To evaluate mechanisms that mediate passage of unconjugated bilirubin (UCB) across placenta, the transport of [ 3 H]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 (∼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.