Figure 1
Figure 1. NKG2A, KIR, and CD57 independently correlate with the proliferative capacity of CD56dim NK cells. (A) Representative staining for CD57 on NK cells from one healthy donor. (B) Representative staining for CFSE and CD57 on NK cells from one healthy donor after 5 days of culture with the indicated cytokines. (C) Frequency of CD57− and CD57+ NK cells diluting CFSE on days 0, 3, 5, and 7 after stimulation with the indicated cytokines (n = 6; mean ± standard error of the mean [SEM]). (D) Histograms of one representative experiment in which the indicated NK-cell subsets were purified by FACS sorting and stimulated with IL-2 for 5 days. (E) Dilution of CFSE on FACS-sorted NK-cell subsets stimulated with IL-2 for 5 days (n = 8; mean). (F) Dilution of CFSE on CD57− and CD57+ NK-cell subsets expressing 0, 1, 2, 3, or 4 KIRs stimulated with IL-2 for 5 days (n = 9 0KIR, 36 1KIR, 54 2KIRs, 36 3KIRs, 9 4KIRs; mean).

NKG2A, KIR, and CD57 independently correlate with the proliferative capacity of CD56dim NK cells. (A) Representative staining for CD57 on NK cells from one healthy donor. (B) Representative staining for CFSE and CD57 on NK cells from one healthy donor after 5 days of culture with the indicated cytokines. (C) Frequency of CD57 and CD57+ NK cells diluting CFSE on days 0, 3, 5, and 7 after stimulation with the indicated cytokines (n = 6; mean ± standard error of the mean [SEM]). (D) Histograms of one representative experiment in which the indicated NK-cell subsets were purified by FACS sorting and stimulated with IL-2 for 5 days. (E) Dilution of CFSE on FACS-sorted NK-cell subsets stimulated with IL-2 for 5 days (n = 8; mean). (F) Dilution of CFSE on CD57 and CD57+ NK-cell subsets expressing 0, 1, 2, 3, or 4 KIRs stimulated with IL-2 for 5 days (n = 9 0KIR, 36 1KIR, 54 2KIRs, 36 3KIRs, 9 4KIRs; mean).

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