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. 2015 Jan 12;97(3):583–598. doi: 10.1189/jlb.4A0714-326R

Figure 6. Phenotypic characterization of freshly isolated Ficoll-isolated kidney lymphocytes. (A) Representative flow cytometric density plots show the proportion of NK cells in the 4 mouse groups. (B) Cumulative data representative of the mean percentage and total number of CD45+NKp46+CD3 cells in all 4 groups. (C) NK cells were gated as CD45+NKp46+CD3 and stained for various NK cell markers. Gates were set by use of unstained or nonspecific mAb isotype controls; a representative staining of each marker is shown. The median fluorescence intensity for each marker was analyzed. (D) NK cells were analyzed for CD11bCD27 subsets, and the percentages of CD11bHighCD27Low, CD11bHighCD27High, and CD11bLowCD27High cells were calculated. Gates for each population were set by use of unstained or nonspecific mAb isotype controls. Data were analyzed with a 2-tailed, unpaired Student’s t-test (mean ± sd; n = 4–6 mice/group in 3–4 independent experiments; **P < 0.01; *P < 0.05).

Figure 6.