Measuring Cytotoxicity by Bioluminescence Imaging Outperforms the Standard Chromium-51 Release Assay
Figure 2
Comparison of cytotoxicity obtained at 2 hours by the chromium release method and BLI method.
Luciferase-transduced human and mouse cell lines were co-cultured with human or mouse effector cells for 2 hours at various E:T ratios. The % specific lysis of the human cell lines, (A) K562, (B) U266, and (C) UCI101 obtained by the chromium release assay (closed circles) or the BLI assay (open circles) is plotted against multiple E:T ratios. The % specific lysis of the human cell lines, (D) P815, (E) YAC1, (F) EL-4, and (G) A20 obtained by the chromium release assay (closed circles) or the BLI assay (open circles) is plotted against multiple E:T ratios. Results are represented as mean ± SD of n = 3 independent experiments. The p values obtained from the statistical analysis performed by permutated two-way ANOVA are shown in each graph.