Figure 1
Figure 1. Engagement of individual activation receptors on resting NK cells induces inside-out signals. Resting NK cells were mixed with target cells as indicated. Where indicated, S2 cells were preincubated with a rabbit anti-S2 serum (+ IgG). Cells were incubated for 5 minutes at 37°C, stained with conformation-specific, biotinylated anti–LFA-1 mAbs, washed, and stained with fluorochrome-conjugated anti-CD56 and streptavidin. (A-B) NK cells were gated on forward scatter/side scatter plots, and the profiles show CD56 versus 327C or mAb24 mAb staining, as indicated. Gates indicate the percentage of 327Chigh or mAb24high NK cells. The profiles are representative of 3 or more independent experiments. (C-D) The percentage of 327Chigh or mAb24high CD56dim NK cells is presented as the mean of 6 donors. Bars indicate SD. *P < .01.

Engagement of individual activation receptors on resting NK cells induces inside-out signals. Resting NK cells were mixed with target cells as indicated. Where indicated, S2 cells were preincubated with a rabbit anti-S2 serum (+ IgG). Cells were incubated for 5 minutes at 37°C, stained with conformation-specific, biotinylated anti–LFA-1 mAbs, washed, and stained with fluorochrome-conjugated anti-CD56 and streptavidin. (A-B) NK cells were gated on forward scatter/side scatter plots, and the profiles show CD56 versus 327C or mAb24 mAb staining, as indicated. Gates indicate the percentage of 327Chigh or mAb24high NK cells. The profiles are representative of 3 or more independent experiments. (C-D) The percentage of 327Chigh or mAb24high CD56dim NK cells is presented as the mean of 6 donors. Bars indicate SD. *P < .01.

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