Figure 5
Figure 5. In vitro hyporesponsiveness of Itgb2Jkr/Jkr NK cells in mixed BM chimeras. Bone marrow cells from WT (CD45.1+; open histograms) or Itgb2Jkr/Jkr (CD45.2+; black histograms) mice were isolated and mixed at an equal ratio before transfer into irradiated WT (CD45.1+) recipients. Splenocytes from chimeric mice were analyzed 16-22 weeks after reconstitution. NK-cell IFN-γ production (A) and degranulation (CD107a exposure; B) were tested by flow cytometry after activation and surface and intracellular stainings. The responsiveness of WT (CD45.1 staining) and CD18-deficient (Itgb2Jkr/Jkr, CD45.2 staining) on stimulation with the tumor YAC-1, NK1.1 monoclonal antibody-coated plates, or PMA/ionomycin was compared after 4 hours of stimulation. Data are expressed as the percentage of IFN-γ+ (A) and the percentage of CD107a+ (B) in the NK cell gate. n = 7 for each genotype, means ± SEM are shown. Statistical analysis was performed using a one-tailed Mann-Whitney test.

In vitro hyporesponsiveness of Itgb2Jkr/Jkr NK cells in mixed BM chimeras. Bone marrow cells from WT (CD45.1+; open histograms) or Itgb2Jkr/Jkr (CD45.2+; black histograms) mice were isolated and mixed at an equal ratio before transfer into irradiated WT (CD45.1+) recipients. Splenocytes from chimeric mice were analyzed 16-22 weeks after reconstitution. NK-cell IFN-γ production (A) and degranulation (CD107a exposure; B) were tested by flow cytometry after activation and surface and intracellular stainings. The responsiveness of WT (CD45.1 staining) and CD18-deficient (Itgb2Jkr/Jkr, CD45.2 staining) on stimulation with the tumor YAC-1, NK1.1 monoclonal antibody-coated plates, or PMA/ionomycin was compared after 4 hours of stimulation. Data are expressed as the percentage of IFN-γ+ (A) and the percentage of CD107a+ (B) in the NK cell gate. n = 7 for each genotype, means ± SEM are shown. Statistical analysis was performed using a one-tailed Mann-Whitney test.

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