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. 2014 Jan 29;9(1):e87086. doi: 10.1371/journal.pone.0087086

Figure 1. NK cell production from fresh and frozen CBCD34+.

Figure 1

(A) Total fold expansion and (B) CD3CD56+ NK cell number of fresh (n = 3) and frozen (n = 4) CBCD34+ cultures at different time points. (C) Intracellular expression of IFN-γ and (D) secreted IFN-γ as measured by ELISA for NK cells from fresh (n = 3) and frozen (n = 4) CBCD34+ cultures. (E) Degranulation assay using CD107a on CD56+CD3 cells from fresh (n = 3) and frozen (n = 4) CBCD34+ cultures. NK cells from fresh (n = 3, solid line) and frozen (n = 4, dotted line) CBCD34+ cultures were co-incubated with 51Cr-labeled K562 cells (F) or 51Cr-labeled P815 cells (G) coated with anti-CD16 or an isotype control at different effector-target ratios in a standard 4 h 51Cr-release assay. The statistical analysis was performed using Mann-Whitney test, * P<0.05, ** P<0.005.