Figure 7
Figure 7. Inflammation enhances DC migration mainly by CCR7-dependent, and moderately by CCR7-independent, mechanisms. FITC painting experiments were performed in the uninflamed or CFA-inflamed ears of WT and CCR7−/− mice. (A) CFA injection induced a similar degree of ear swelling in WT and CCR7−/− mice. (B) LN single-cell suspensions were analyzed by FACS for the presence of I-A/I-E+CD11c+FITC+ cells. The number within each plot represents the percentage of gated cells. (C) Inflammation further enhanced the CCR7 dependence of DC migration, as demonstrated by the quantification of total numbers of I-A/I-E+CD11c+FITC+ cells. Numbers indicate the fold difference in DC migration observed in WT compared with CCR7−/− mice. (D) Inflammation also enhanced DC migration in CCR7−/− mice, as evidenced by the quantification of total numbers of I-A/I-E+CD11c+FITC+ cells in the dLNs. **P < .01. ***P < .001.

Inflammation enhances DC migration mainly by CCR7-dependent, and moderately by CCR7-independent, mechanisms. FITC painting experiments were performed in the uninflamed or CFA-inflamed ears of WT and CCR7−/− mice. (A) CFA injection induced a similar degree of ear swelling in WT and CCR7−/− mice. (B) LN single-cell suspensions were analyzed by FACS for the presence of I-A/I-E+CD11c+FITC+ cells. The number within each plot represents the percentage of gated cells. (C) Inflammation further enhanced the CCR7 dependence of DC migration, as demonstrated by the quantification of total numbers of I-A/I-E+CD11c+FITC+ cells. Numbers indicate the fold difference in DC migration observed in WT compared with CCR7−/− mice. (D) Inflammation also enhanced DC migration in CCR7−/− mice, as evidenced by the quantification of total numbers of I-A/I-E+CD11c+FITC+ cells in the dLNs. **P < .01. ***P < .001.

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