Figure 2
Figure 2. LFA-1 molecule is a marker of NK cell differentiation. (A) Flow cytometry analysis of LFA-1 expression on CD161+CD56+CD117+CD94/NKG2A− (light gray line, empty profile), CD161+CD56+CD117lowCD94/NKG2A+ (bold black line, empty profile), CD161+CD56+CD117−CD94/NKG2A+ (gray profile) cells. (B) After 20 days of culture, in vitro derived NK cells were analyzed for the expression of activating receptors gating separately on CD161+CD56+LFA-1− cells (gray line, gray profile) or CD161+CD56+LFA-1+ cells (black line, empty profile). Dashed line in histograms indicates isotype control. (C) CD161+CD56+LFA-1− immNK cells and CD161+CD56+LFA-1+ difNK cells were isolated by cell sorting and analyzed for their cytotoxic activity in a 4-hour 51Cr release assay against melanoma FO1 cell line. The E/T ratio was 5/1.

LFA-1 molecule is a marker of NK cell differentiation. (A) Flow cytometry analysis of LFA-1 expression on CD161+CD56+CD117+CD94/NKG2A (light gray line, empty profile), CD161+CD56+CD117lowCD94/NKG2A+ (bold black line, empty profile), CD161+CD56+CD117CD94/NKG2A+ (gray profile) cells. (B) After 20 days of culture, in vitro derived NK cells were analyzed for the expression of activating receptors gating separately on CD161+CD56+LFA-1 cells (gray line, gray profile) or CD161+CD56+LFA-1+ cells (black line, empty profile). Dashed line in histograms indicates isotype control. (C) CD161+CD56+LFA-1 immNK cells and CD161+CD56+LFA-1+ difNK cells were isolated by cell sorting and analyzed for their cytotoxic activity in a 4-hour 51Cr release assay against melanoma FO1 cell line. The E/T ratio was 5/1.

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