Dose response curves were measured in triplicate, and controls (1 nM dihydrotestosterone (DHT) Thiazovivin manufacturer and 0.1% ethanol, respectively) were repeated 6-fold. Measurement of luciferase activity was performed in cellular crude extracts using a Synergy HT plate reader from BioTek (Bad Friedrichshall, Germany). Cells were lysed in situ using 50 μl of lysis buffer (0.1 M tris–acetate, 2 mM EDTA, and 1% triton-x, pH 7.8), shaking the plate moderately for 20 min at room temperature. Following cellular lysis 150 μl

of luciferase buffer (25 mM glycylglycine, 15 mM MgCl2 and 4 mM EGTA, 1 mM DTT, 1 mM ATP, pH 7.8) and 50 μl of luciferin solution (25 mM glycylglycine, 15 mM MgCl2 and 4 mM EGTA, 0.2 mM luciferin, pH 7.8) were added automatically to each well in order to measure luminescence. All values were corrected for the mean of the negative control and then related to the positive control which was set to 100%. Cell line HeLa9903 was obtained from the JCRB (JCRB-No. 1318). These cells contain stable expression constructs for human ERα and firefly luciferase, respectively. The selleck chemical latter is under transcriptional control of five ERE promoter elements from the vitellogenin gene. The transcription of ERα was confirmed by RT-PCR, as was the absence of AR-transcripts (Fig. S1). The assay was performed according

to the OECD test guideline TG455 (OECD, 2009) as follows. Cells were cultivated in phenol red free MEM containing 10% (v/v) of charcoal stripped FCS at 37 °C in an atmosphere with 5% CO2. For the actual assay cells were seeded into white 96-well polystyrene plates at a concentration of 104 cells per 100 μl and well (Costar/Corning, Amsterdam, Netherlands). Test substances were added 3 h after seeding by adding 50 μl of triple concentrated substance stocks to each well. As before dose response curves for treated samples were measured Orotidine 5′-phosphate decarboxylase in triplicate, while controls (1 nM E2 or 0.1% ethanol, respectively) were repeated 6-fold. After 24 h of stimulation, cells were washed with PBS and then lysed using 50 μl

of lysis buffer and moderate shaking for 20 min at room temperature. Subsequent measurement of luciferase activity was performed analogous to the aforedescribed androgen reporter gene assay. All values were corrected for the mean of the negative controls and then related to the positive controls set as 100%. Cell line MCF-7 was obtained from the ATCC (ATCC-No. HTB-22) and checked with RT-PCR for transcription of ER, AR, GPR30 and AhR (Fig. S1). Cells were routinely passaged in RPMI 1640 medium containing 10% FCS (v/v), 100 U/ml Penicillin and 100 μg/ml streptomycin and grown at 37 °C in an atmosphere with 5% CO2. Prior to the actual assays the cells were transferred into hormone-free medium (phenol red free RPMI 1640 with 5% of charcoal stripped FCS).