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. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Adv Biol (Weinh). 2022 Apr 7;6(9):e2200019. doi: 10.1002/adbi.202200019

Figure 6. Increased immune cell infiltrate in CGRPKO mice.

Figure 6.

Using flow cytometry, tumor infiltrating and lymph node lymphocyte subsets were quantified in dissociated tongue tissue from wildtype mice (black, n=4) and CGRPKO (white, n=4) from MOC1-tumor bearing mice at PID 21 (A,B) and MOC2-tumor bearing mice at PID 7 (C,D). Data are presented as a percent change from genotype-matched sham mice (n=4 per genotype). Two-way ANOVA, *p<0.05 **p<0.01. The percent of CD45+ immune cells quantified for both sham and tumor-bearing mice are available in Table 2. E) Representative gating strategy used to isolate tongue tumor infiltrating T cells by fluorescence-activated cell sorting (FACS). F) Quantification of Ramp1 expression in CD4+ T cells isolated from tongue or lymph node tissue from sham (white, n=4/time point), MOC1-tumor bearing mice (gray, n=4 PID 35), or MOC2-tumor bearing mice (gray, n=4, PID 14) relative to housekeeping gene Gapdh. Student’s t test *p<0.05, **p<0.01.