| Literature DB >> 27616577 |
Tomoya Akashi1, Tomohiro Nishimura1, Yoshiya Takaki1, Masaya Takahashi1, Bo-Chul Shin2, Masatoshi Tomi3, Emi Nakashima1.
Abstract
The purpose of this study is to clarify the subcellular localizations of multidrug resistance protein 1 (MDR1)/ABCB1 and breast cancer resistance protein (BCRP)/ABCG2 in the rodent placental SynT bilayer, i.e., a maternal-facing (SynT-I) layer and a fetal-facing (SynT-II) layer. In double immunofluorescence staining, the signals of MDR1 and BCRP appeared midway between the signals of glucose transporter 1 on the apical membrane of SynT-I and the basal plasma membrane of SynT-II, and mostly overlapped with signals of connexin 26, which forms gap junctions between SynT-I and SynT-II. In detail, median intensities (pixels) of the MDR1 and BCRP signals were significantly closer to the fetal circulation as compared to the location of connexin 26 signals. In double in situ hybridization studies, the signals of Mdr1b mRNA mostly overlapped with those of Syncytin-B, a SynT-II marker. In conclusion, MDR1 and BCRP are expressed on apical membranes of the rodent placental SynT-II layer.Entities:
Keywords: BCRP; MDR1; Placental barrier; Rodent; Syncytiotrophoblast; Transporter
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Year: 2016 PMID: 27616577 DOI: 10.1016/j.reprotox.2016.09.002
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143