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. 2010 Sep 22;300(1):F62–F70. doi: 10.1152/ajprenal.00473.2010

Fig. 7.

Fig. 7.

Effect of P2X7 inhibition on cell supernatant-induced cell death in NRK-49F cells. NRK-49F cells were incubated with different concentration (0.5–2 μM) of A438079 for 1 h and then treated with cell supernatant for 20 h, and cell viability was assessed the MTT assay (A). Cells were treated with supernatant for 20 h in the presence or absence of 1 μM of A438079 and then harvested for immunoblot analysis for P2X7, active PARP, cleaved caspase-3, and actin (B). NRK-49F cells were transfected with siRNA targeting P2X7 or scrambled siRNA and allowed to grow for 24 h and then treated with supernatant for 20 h. Cell viability was assessed by the MTT assay (C), and cell lysates were subjected to immunoblot analysis for P2X7, cleaved PARP, cleaved caspase-3, and actin (D). Values are means ± SD of 3 independent experiments. Bars with different letters (a–c) are significantly different from one another (P < 0.05).