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. 1999 Nov;155(5):1701–1711. doi: 10.1016/S0002-9440(10)65485-5

Table 2.

GEC Cytotoxicity

A BCECF-specific release (%)
5% vol/vol 2.5% vol/vol 1.25% vol/vol
Normal serum 77 ± 4* 52 ± 4* 20 ± 3*
C8DS+C8 55 ± 7 17 ± 7 9 ± 5
B LDH-specific release (%)
10% vol/vol 5% vol/vol 2.5% vol/vol
Normal serum 61 ± 9 17 ± 8 0 ± 0
Normal serum+ AG1478 67 ± 11 19 ± 7 0 ± 0

A: GEC were incubated with BCECF-acetoxymethyl ester and then incubated with either antibody and complement (normal serum or C8DS+C8) or heat-inactivated serum in controls. Supernatants were collected and cells were permeabilized with digitonin to release remaining BCECF. BCECF content was measured by spectrofluorometry. Specific release is calculated as (E − C)/(100 − C), where E is the percent released in complement-treated cells and C is the percent released in control incubations (heat-inactivated serum). Significantly greater BCECF release was present in normal serum groups, as compared with C8DS+C8 groups (*P < 0.0001 ANOVA; 3 experiments).

B: GEC were incubated with or without AG1478, 300 nmol/L and with antibody and normal serum, or with heat-inactivated serum in controls. Supernatants were collected and cells were permeabilized with digitonin to release remaining lactate dehydrogenase (LDH). LDH activity was assayed in supernatants and digitonin-treated cells, and specific release was calculated as above. There are no significant differences between AG1478-treated and untreated groups (4 experiments).