Fig. 1From: High and selective cytotoxicity of ex vivo expanded allogeneic human natural killer cells from peripheral blood against bladder cancer: implications for natural killer cell instillation after transurethral resection of bladder tumorCytotoxicity, degranulation activity, and cytokine secretion of the expanded NK cells. (A) Killing rates of the NK cells against multiple BCa cell lines (including BIU-87, T24, UMUC-3, and 5637) and normal epithelial cell line SV-HUC-1 at different E:T ratios after 0.5, 1, and 2 h coculture (n = 3); (B) Comparison of supernatant IFN-γ levels between NK cells cocultured with BCa cells (T24 or 5637) and their counterparts cocultured with normal epithelial cell line SV-HUC-1 at different E:T ratios after 0.5, 1, and 2 h coculture (n = 3); (C) Representative flow cytometry plots and summary data of CD107a expression on the NK cells after coculture with BCa cells, normal epithelial cells, and NK cells alone for 1 h (n = 3). E:T = 10:1; (D) Comparison of supernatant perforin and granzyme B levels between NK cells cocultured with BCa cells and their counterparts cocultured with normal epithelial cells at E:T of 10:1 after 1 h coculture (n = 3). NK cells alone were set as negative control. E Comparison of supernatant IFN-γ and TNF levels between NK cells cocultured with BCa cells and their counterparts cocultured with normal epithelial cells at E:T of 10:1 after 1 h coculture (n = 3). NK cells alone were set as negative control. Data expressed as means ± SD were plotted, and ANOVA followed by a Tukey’s post hoc test were used to compare three or more groups (A–E). *p < 0.05; ns, not significant. Abbreviations: BCa: bladder cancer; E:T: effector-to-target ratio; TNF: tumor necrosis factorBack to article page