1 mL of PBS) was added to each well. The cells were incubated at 37°C for 4 h, and DMSO (100 μL) was added to dissolve the formazan crystals. The absorbance rate of each well optical density (OD value) was measured at 570 nm by a spectrophotometer. The cell proliferation inhibition rate was calculated as 1-(average OD value of wells with administered drug/average OD value of control wells)×100. To explore the possibility that NCTD induced intracellular ROS in antiproliferation, the HepG2 cells were pretreated with NAC
(10 mM) 2 h before treatment with NCTD, followed by NCTD (5,10,20,40 μg/ml) treatment for 24 h. HepG2 cells proliferation response was determined by MTT assay as described above. The experiments and all the below assays were repeated thrice. Annexin V/PI Staining Assay To quantify the Mocetinostat in vitro percentage of cells undergoing apoptosis, we used Annexin V-FITC kit. HepG2 cells were incubated for 24 h with NCTD (10,20,40 μg/ml). Then the cells were washed twice with cold PBS and resuspended in binding buffer at a concentration of 1 × 106 cells/ml. After incubation, 100 μl of the solution was transferred to a 5 ml culture tube, and 5 μl of Annexin V-FITC and 10 μl of PI were added. The tube was gently vortexed and incubated for 15 minutes at room temperature in the dark. At the end of incubation, 400 μl of binding buffer was added, and the cells were analyzed immediately by flow cytometry. Flow
cytometry analysis was performed using the Cell Quest software. Analysis of ROS production Selleckchem BMS202 The intracellular ROS level was detected by flow cytometry using DCHF-DA. DCHF-DA is a stable fluorescent ROS-sensitive compound, which readily
diffuses into cells. DCHF-DA is hydrolyzed by esterase to form DCHF within cells, which is oxidized by hydrogen peroxide or low-molecular-weight peroxides to produce the fluorescent compound 2′,7′-dichlorofluorescein(DCF). In the present study, HepG2 cells were treated with NCTD (10, 20, 40 μg/ml) for 6 h, followed by staining with DCHF-DA (100 μM) for an additional 30 min. Green fluorescence in cells under different treatments was analyzed by flow cytometry analysis. NAC(10 mM) was added 1 h prior to the (-)-p-Bromotetramisole Oxalate treatment with 20 μg/ml NCTD for 6 h. Measurement of Mitochondrial Membrane Potential(Δφm) The loss of Δφm was monitored with the dye JC-1. JC-1 is capable of selectively entering mitochondria, where it forms monomers and emits green fluorescence when Δφm is relatively low. At a high Δφm, JC-1 aggregates and gives red fluorescence. The ratio between green and red fluorescence provides an estimate of Δφm that is independent of the mitochondrial mass. Briefly, HepG2 cells (1 × 106 cells/ml) in 10-cm culture dishes were treated without or with NCTD (10,20,40 μg/ml) for 24 h. Cells were trypsinized, washed in ice-cold PBS, and incubated with 10 mM JC-1 at 37°C for 20 min in darkness. Subsequently, cells were washed twice with PBS and analyzed by flow cytometry.