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. 2021 Nov 24;22(23):12712. doi: 10.3390/ijms222312712

Figure 5.

Figure 5

CXCR3 targeting alters CXCL9-mediated CD8+ T cells chemotaxis in Gba19V/− mice. CD8+ T cells purified from spleens of WT and Gba19V/− mice (n = 5/group) were allowed to migrate towards CXCL9 (16 nM) in the presence and absence of mouse anti-CXCR3 antibodies (10 μg/mL) at 37 °C and 5% CO2 for 45 min. Cells that had migrated through the filter and had attached to the lower side of the filter were collected and analyzed by FACS. Percentage of CD8+CD11b T cells are shown from the (a) vehicle (PBS) treated WT cells and their migration to CXCL9, (b) mouse anti-CXCR3 antibodies treated WT cells and their migration to CXCL9, (c) PBS treated Gba19V/− cells and their migration to CXCL9, and (d) mouse anti-CXCR3 antibodies treated Gba19V/− cells and their migration to CXCL9. (e) WT (black columns), Gba19V/− (maroon columns) and the values shown in the bar diagram are the mean ± SD. and group comparison was performed with ANOVA. Three independent experiments were conducted (**** p < 0.0001).