Fig. 1.
Fig. 1. Fas susceptibility and EBV status of cell lines used in this study. Fas-mediated apoptosis was assayed with MTT. Triplicate cultures of 100 μL (3 × 104 cells) were incubated with anti-Fas IgM (250 ng/mL) for 24 hours at 37°C. MTT was then added for an additional 2 hours followed by solubilization of the formazan crystals. Absorbance was read at 570 nmol/L and percentage apoptosis was calculated as previously described.40 Results are from 3 separate experiments and are expressed as mean percentage apoptosis ± standard deviation. Cell-surface expression of the Fas receptor was determined by flow cytometry and the results indicate Fas-positive (▪) and Fas-negative (□) cell lines. The EBV status (negative or positive) of each cell line was obtained from the literature and later confirmed in appropriate cell lines by LMP1 immunoblot analysis.6162

Fas susceptibility and EBV status of cell lines used in this study. Fas-mediated apoptosis was assayed with MTT. Triplicate cultures of 100 μL (3 × 104 cells) were incubated with anti-Fas IgM (250 ng/mL) for 24 hours at 37°C. MTT was then added for an additional 2 hours followed by solubilization of the formazan crystals. Absorbance was read at 570 nmol/L and percentage apoptosis was calculated as previously described.40 Results are from 3 separate experiments and are expressed as mean percentage apoptosis ± standard deviation. Cell-surface expression of the Fas receptor was determined by flow cytometry and the results indicate Fas-positive (▪) and Fas-negative (□) cell lines. The EBV status (negative or positive) of each cell line was obtained from the literature and later confirmed in appropriate cell lines by LMP1 immunoblot analysis.61,62 

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