Figure 2.
Figure 2. Role of ITAM-bearing subunits in NK cell effector functions. (A-B) polyIC NK cells were purified from control (CTR) and mutant mice and used as effectors against indicated tumor cells. Data shown are representative of at least 4 independent experiments. (C-D) Mice were injected intravenously with 3 × 105 cells of B16, B16-H60, or B16-Rae1β melanoma cells, and total lung metastases were counted 2 weeks after tumor challenge. Dots indicate data from individual mice: ○, control mice (CTR); •, DAP12KI mice. Horizontal bars indicate mean values. Statistical analysis was performed using unpaired Student t test. (E) NKG2D tetramer staining (filled histograms) is represented in comparison with staining with an irrelevant KIR2DL3 tetramer (empty histograms).63 Cytotoxicity experiments were performed as described in panels A and B. Blocking experiments were performed by adding anti-NKG2D (MI-6, rat IgG2a) or isotype control mAb at a final concentration of 50 μg/mL, during the 4-hour cytotoxicity assay. (F) Percentages of IFN-γ+ cells in gated CD3–NK1.1+ cells; □ indicate polyIC NK cells from C57BL/6 mice; ▪, polyIC NK cells from DAP12KI mice. IFN-γ+ NK cells were not detectable in cells stimulated with B16 melanoma cells. (G) Percentages of IFN-γ+ cells in mixed bone marrow chimera reconstituted with RAGKO and ZGR precursors were analyzed on NK cell subsets phenotypically defined, as described in legend to Figure S1; □ indicate percentages of IFN-γ+ cells gated in CD3–NK1.1bright2B4+ (NK cells from RAGKO); ▪, percentages of IFN-γ+ cells gated in CD3–NK1.1dim2B4– (NK cells from ZGR mice). Stimulation with target cells was performed at an effector-target (E/T) ratio of 1:1. Ly49D triggering was performed on high-affinity 96-well plates (Immulon, Labsytems, VWR, France) precoated with isotype control antibodies or with anti-Ly49D (4E5) at the final concentration of 50 μg/mL. Values obtained with control antibodies were subtracted from values obtained with Ly49D stimulation. Data are representative of at least 2 experiments. Error bars represent SEM.

Role of ITAM-bearing subunits in NK cell effector functions. (A-B) polyIC NK cells were purified from control (CTR) and mutant mice and used as effectors against indicated tumor cells. Data shown are representative of at least 4 independent experiments. (C-D) Mice were injected intravenously with 3 × 105 cells of B16, B16-H60, or B16-Rae1β melanoma cells, and total lung metastases were counted 2 weeks after tumor challenge. Dots indicate data from individual mice: ○, control mice (CTR); •, DAP12KI mice. Horizontal bars indicate mean values. Statistical analysis was performed using unpaired Student t test. (E) NKG2D tetramer staining (filled histograms) is represented in comparison with staining with an irrelevant KIR2DL3 tetramer (empty histograms).63  Cytotoxicity experiments were performed as described in panels A and B. Blocking experiments were performed by adding anti-NKG2D (MI-6, rat IgG2a) or isotype control mAb at a final concentration of 50 μg/mL, during the 4-hour cytotoxicity assay. (F) Percentages of IFN-γ+ cells in gated CD3NK1.1+ cells; □ indicate polyIC NK cells from C57BL/6 mice; ▪, polyIC NK cells from DAP12KI mice. IFN-γ+ NK cells were not detectable in cells stimulated with B16 melanoma cells. (G) Percentages of IFN-γ+ cells in mixed bone marrow chimera reconstituted with RAGKO and ZGR precursors were analyzed on NK cell subsets phenotypically defined, as described in legend to Figure S1; □ indicate percentages of IFN-γ+ cells gated in CD3NK1.1bright2B4+ (NK cells from RAGKO); ▪, percentages of IFN-γ+ cells gated in CD3NK1.1dim2B4 (NK cells from ZGR mice). Stimulation with target cells was performed at an effector-target (E/T) ratio of 1:1. Ly49D triggering was performed on high-affinity 96-well plates (Immulon, Labsytems, VWR, France) precoated with isotype control antibodies or with anti-Ly49D (4E5) at the final concentration of 50 μg/mL. Values obtained with control antibodies were subtracted from values obtained with Ly49D stimulation. Data are representative of at least 2 experiments. Error bars represent SEM.

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