Figure 6
Figure 6. B220+ NK cells exhibit close homology to CD27+ NK cells. (A) Gating strategy for sorting B220+, CD27+, and CD27− NK-cell subsets from the spleen of B6.Rag1−/− mice. B220+ NK cells are selected as CD11clowB220+CD122+ cells, whereas CD27+ and CD27− NK-cell subsets are CD11c−/lowB220−CD122+ cells and are further separated according to CD27 expression. (B) The function of B220+, CD27+, and CD27− NK-cell subsets from B6.Rag1−/− mice is depicted by their cytotoxic activity toward 51Cr-labeled YAC-1 cells. The percentage-specific lysis is shown for B220+ NK cells (round), CD27+ NK cells (square), and CD27− NK cells (triangle). Results are representative of ≥ 3 experiments. (C-D) Hierarchical clustering of differentially expressed genes among B220+, CD27+, and CD27− NK-cell subsets. Three hundred twenty-six genes with an adjusted P value < .05 and an absolute fold change > 1.5 in any of the 2 comparisons (CD27+ vs B220+; CD27− vs B220+) were considered differentially expressed. (C) Gene clustering heat map is shown with the red-green scale presenting the z-transformed intensities whereby red represents a relative increase in expression and green represents a relative decrease. (D) a sample clustering dendrogram is represented from data in panel C.

B220+ NK cells exhibit close homology to CD27+ NK cells. (A) Gating strategy for sorting B220+, CD27+, and CD27 NK-cell subsets from the spleen of B6.Rag1−/− mice. B220+ NK cells are selected as CD11clowB220+CD122+ cells, whereas CD27+ and CD27 NK-cell subsets are CD11c−/lowB220CD122+ cells and are further separated according to CD27 expression. (B) The function of B220+, CD27+, and CD27 NK-cell subsets from B6.Rag1−/− mice is depicted by their cytotoxic activity toward 51Cr-labeled YAC-1 cells. The percentage-specific lysis is shown for B220+ NK cells (round), CD27+ NK cells (square), and CD27 NK cells (triangle). Results are representative of ≥ 3 experiments. (C-D) Hierarchical clustering of differentially expressed genes among B220+, CD27+, and CD27 NK-cell subsets. Three hundred twenty-six genes with an adjusted P value < .05 and an absolute fold change > 1.5 in any of the 2 comparisons (CD27+ vs B220+; CD27 vs B220+) were considered differentially expressed. (C) Gene clustering heat map is shown with the red-green scale presenting the z-transformed intensities whereby red represents a relative increase in expression and green represents a relative decrease. (D) a sample clustering dendrogram is represented from data in panel C.

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