Analysis of drug transporter expression in syncytiotrophoblast derived from human placental stem cells: Expression and function of efflux transporters
Riko Sawada, Ayako Furugen, Ayami Ueda, Ayako Nishimura, Takeshi Umazume, Katsuya Narumi, Masaki Kobayashi
Abstract
The placenta is a vital organ for exchanging nutrients, endogenous substances, and xenobiotics between mother and fetus. The syncytiotrophoblast (ST) is crucial in maintaining the placental barrier. Human trophoblast stem cells (hTSCs) have been recently established; however, their utility in studying placental transport functions has not been fully elucidated. This study investigated the expression and function of transporters in hTSC-derived ST cells. TS CT cells, as hTSCs, were differentiated into ST-like cells (ST-TS CT ), and the gene expression of 84 transporters in ST-TS CT cells was evaluated using a PCR array. BeWo cells, a widely used trophoblast model, were used for comparison. BeWo cells were differentiated into ST-like cells using forskolin [BeWo (FK)]. The protein levels of efflux transporters were examined by western blotting, and functional assays were performed using typical fluorescent substrates. Transporter gene expression levels were higher in ST-TS CT than in BeWo (FK) cells, with 27 genes showing more than a 3-fold increase. Ten of these genes were exclusively expressed in ST-TS CT . Western blotting revealed the presence of efflux transporters, including P-glycoprotein (P-gp/ ABCB1 ), breast cancer resistance protein (BCRP/ ABCG2 ), and multidrug resistance-associated protein 2 (MRP2/ ABCC2 ). Furthermore, the accumulation of typical substrates (Rhodamine123 for P-gp, Hoechst33342 and BODIPY™ FL Prazosin for BCRP, and 5(6)-carboxy-2′,7′-dichlorofluorescein diacetate for MRP) significantly increased when transporter inhibitors (elacridar, Ko143, and MK571) were applied. This study showed higher transporter expression in ST-TS CT than that in a traditional trophoblast model. Furthermore, the functional expression of efflux transporters was observed. ST-TS CT is valuable for investigating placental transport functions. • The expression of 84 transporters in ST-TS CT was evaluated using a PCR array. • Transporter gene expression was generally higher in ST-TS CT than in BeWo cells. • P-gp/ ABCB1 , BCRP/ ABCG2 , and MRP2/ ABCC2 were expressed in ST-TS CT . • An accumulation assay revealed the efflux functions of these transporters in ST-TS CT .