As shown in Figure 4, cells showed more negative staining than co

As shown in Figure 4, cells showed more negative staining than control group after BSO pretreatment and NAC decreased the inhibition. The results were basically consistent with Western blot result. Figure 4 The change of HIF-1α expression by ICC

assay. (A) The picture of ICC was shown. a: negative control; b: normoxic control; c: hypoxic control; d: the hypoxic cells by 50 μM BSO pretreatment; e: the hypoxic cells by 100 μM BSO pretreatment; f: the hypoxic cells by 200 μM BSO pretreatment; g: the hypoxic cells by 50 μM BSO + 5 mM NAC pretreatment; j: the hypoxic cells by 100 μM BSO + 5 mM NAC pretreatment; k: the hypoxic cells by 200 μM BSO + 5 mM NAC pretreatment. (B) The results of statistical Selleck CBL0137 analysis were shown with H-score values of semi-quantitative evaluations. www.selleckchem.com/products/XAV-939.html (◆ P <0.05, # p < 0.01, compared with hypoxic control; *P <0.05, compared with the hypoxic cells by 5 mM NAC pretreatment). Changes of genes targeted by HIF-1 The levels of MDR-1 and EPO transcription were detected

through semi-quantitative RT-PCR. The results displayed that the levels of MDR-1 and EPO mRNA were declined in hypoxic cells when BSO concentration was at 50 μM, but it wasn’t shown that there was a statistical significance at the MDR-1 and EPO mRNA of 50 μM BSO pretreatment compared with those of the hypoxic control. Concomitant with the increases of BSO concentrations, the levels of MDR-1 and EPO mRNA in hypoxic cells were gradually decreased. Kinase Inhibitor Library solubility dmso And then the inhibitory effects on MDR-1 and EPO mRNA, BSO concentrations reaching at 100 μM and 200 μM respectively, were shown statistical differences. Urease Meanwhile, NAC could reduce the inhibition of BSO to MDR-1 and EPO mRNA. Furthermore, the expression of P-gp by MDR-1 translation, tested with western

blotting, was also confirmed with the change of MDR-1 mRNA. Above experimental results were displayed in Figure 5 and Figure 6. It is therefore clear that redox micro-environment may influence the levels of target genes located at the downstream of HIF-1. Figure 5 The changes of MDR-1 expressions by RT-PCR and Western blotting measurement. Letter N means the cells under normoxic condition; Letter H means the cells under hypoxic condition: (A) The representative gel picture was taken from three separate RT-PCR experiments. (B) Compared with hypoxic control, the analysis of relative densities showed that there was statistical difference the experimental cells by 100 and 200 μM BSO pretreatment respectively (# p < 0.01). After NAC incubation, the expression of MDR-1 was elevated again, and there were significant difference between the group with 100 μM NAC treatment and that without NAC treatment (▲ P < 0.05). (C) The representative gel picture was taken from three separate Western blotting experiments.

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