Figure 6.
Figure 6. Enhanced NKR-P1C-induced signaling in MIST-deficient NK cells. (A) NKR-P1C-induced intracellular calcium flux in MIST-deficient NK cells. Wild-type (+/+) and MIST-deficient (-/-) NK cells loaded with Indo 1-AM were stimulated with anti-NK1.1 antibody. The ratio of fluorescence detected in FL5-FL4 was monitored by flow cytometry. Acquisition was interrupted once to add cross-linking goat F(ab′)2 antibody (arrows) and again to add 1 μg/mL ioomycin (arrowheads). (B) Enhanced phosphorylation of PLCγ2, ERK, and p38 MAP kinases in MIST-deficient NK cells upon NKR-P1C stimulation. Cell lysates from wild-type (+/+) and MIST-deficient (-/-) NK cells stimulated with anti-NK1.1 antibody were immunoblotted with the indicated antibodies. Figures give induction levels over zero time points, determined by densitometry after normalizing for loading.

Enhanced NKR-P1C-induced signaling in MIST-deficient NK cells. (A) NKR-P1C-induced intracellular calcium flux in MIST-deficient NK cells. Wild-type (+/+) and MIST-deficient (-/-) NK cells loaded with Indo 1-AM were stimulated with anti-NK1.1 antibody. The ratio of fluorescence detected in FL5-FL4 was monitored by flow cytometry. Acquisition was interrupted once to add cross-linking goat F(ab′)2 antibody (arrows) and again to add 1 μg/mL ioomycin (arrowheads). (B) Enhanced phosphorylation of PLCγ2, ERK, and p38 MAP kinases in MIST-deficient NK cells upon NKR-P1C stimulation. Cell lysates from wild-type (+/+) and MIST-deficient (-/-) NK cells stimulated with anti-NK1.1 antibody were immunoblotted with the indicated antibodies. Figures give induction levels over zero time points, determined by densitometry after normalizing for loading.

Close Modal

or Create an Account

Close Modal
Close Modal