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. 2013 Jun 11;8(6):e65599. doi: 10.1371/journal.pone.0065599

Figure 9. Lysis of B16 melanoma by hepatic NK cell subsets.

Figure 9

B6 mice were given CpG i.p, their livers were harvested 48 hrs later, a mononuclear cell preparation obtained and labelled with CD5, NK1.1, CD27 and CD11b. Software gates were set on NK cells and the resulting four subsets of CD27 and CD11b dual label were sorted and used in a 4 hr 51Cr-release assay against B16 melanoma targets. Lytic units were calculated with one lytic unit defined as the number of effector cells needed to effect 30% specific lysis. The values on the X-axis are lytic units per 1×106 effector cells. The lytic potential of the CD27hi/CD11blo subset was statistically significant when compared to the CD27loCD11blo (p = 0.03) and the CD27loCD11bhi (p = 0.028) but not when compared to the CD27hiCD11bhi subset.