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. 2011 Feb 17;7(2):e1001291. doi: 10.1371/journal.ppat.1001291

Figure 2. Expression of RV capsid protein blocks activation of caspase 3.

Figure 2

A. A549 cells were transiently transfected with plasmids encoding eGFP, RV glycoproteins E2 and E1, capsid protein or the anti-apoptotic protein Bcl-XL. At forty hours post-transfection, cells were treated with anti-Fas for 6 hours after which time they were processed for immunofluorescence using rabbit anti-caspase 3 and mouse antibodies to E1, capsid or Bcl-XL. Primary antibodies were detected with donkey anti-rabbit Alexa488 and chicken anti-mouse Alexa594. For samples expressing eGFP, the rabbit anti-caspase 3 was detected with donkey anti-rabbit conjugated to Texas Red. Nuclei were counter stained with DAPI. Scale bar  = 10 µm. B. The percentages of transfected cells expressing active caspase 3 (double positive) were determined and plotted. Error bars indicate standard deviations calculated from three independent experiments in which at least 100 cells for each experiment were scored. One-way ANOVA was used to determine statistical significance. p = ≤0.001.