The isolated RNA was Talazoparib order then DNase-treated and reverse-transcribed according to the manufacturer’s instructions. To detect gC1qR expression, Primer-F (5′-AAT CAC ACG GTA GAC ACT GAA ATG CC-3′) and Primer-R (5′-CAT CAT CCC ATC TAA AAT GTC CCC TG-3′) were used with the FAM/TAMRA-labelled probe 5′-TGC TCC AGT TCA ACC AAC GTC CTT CTC-3′. β-actin was quantified using Primer-F (5′-TCA CCC ACA CTG TGC CCA TCT ATG A-3′) and Primer-R (5′-CAT CGG AAC CGC TCA TTG CCG ATA G-3′) with the FAM/TAMRA-labelled probe 5′-ACG CGC TCC CCC ATG CCA TCC TGC GT-3′. Quantitative real-time PCR was performed using an ABI PRISM 7300 sequence detection system with the following thermal cycling

conditions: 2 min at 50°C and 10 min at 95°C, followed by a total of 40 cycles of 15 s at 95°C and 1 min at 60°C. All of the reactions were performed in 50-μL reaction volumes in triplicate. Standard curves were generated for gC1qR and β-actin. The β-actin gene was used as an internal control in all of the PCR experiments. The relative amounts of gC1qR mRNA were normalized

to β-actin mRNA using the following formula: Following specific treatments, the HTR-8/SVneo and HPT-8 cells were collected and placed in sample buffer and then incubated in lysis buffer containing 150 mm NaCl, 1 mm Na3VO4, 50 mm NaF, 1% Triton X-100, 1 mm EDTA, 1 mm PMSF, 10% glycerol, 20 mm Tris–HCl (pH 7.5) and protease inhibitors for 30 min on ice. The supernatants were collected following centrifugation at 13,000× g

at 4°C for 15 min. Equal amounts of protein were separated by SDS-PAGE on a 10–15% check details polyacrylamide gel and transferred onto a PVDF membrane. The membranes were then blocked for 1 hr in 5% non-fat milk in PBST (PBS containing 0.05% Tween-20) and incubated with the appropriate primary antibodies and horseradish peroxidase-conjugated secondary antibodies. The protein bands were visualized using the enhanced chemiluminescence (ECL) Western Detection System. The production of ROS was measured using the cell-permeable probe, H2DCFDA, which preferentially measures peroxides. Briefly, HTR-8/SVneo and HPT-8 cells were grown on cover slips and incubated Histidine ammonia-lyase with H2DCFDA (10 μm) under various conditions for 15 min in the dark and lysed with RIPA buffer under ice-cold conditions.[17] H2DCFDA fluorescence was detected using fluorescence microscopy at an excitation wavelength of 488 nm and an emission wavelength of 530 nm. A spectrofluorometer with a slit width of 5 nm was used to quantify the level of fluorescence in the supernatant. The experiments were repeated at least ten times. The results were determined according to the increase in fluorescence intensity with respect to normoxic untreated controls by subtracting the basal fluorescence levels. Fluorescence from Fluo-4 AM was used to quantify the intracellular Ca2+ levels.