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. 2011 Mar;178(3):1201–1209. doi: 10.1016/j.ajpath.2010.11.073

Table 1.

Characterization of Cellular Infiltrate in CG-Treated Paws of WT and Gal-1−/− Mice

Marker Time (hours) Control (1 × 105/paw) WT (1 × 105/paw) Gal-1−/− (1 × 105/paw)
GR-1/CD11b 48 0.29 ± 0.05 9.72 ± 1.43 4.25 ± 1.23
96 0.16 ± 0.02 0.53 ± 0.18 0.64 ± 0.10
CD11c/CCR7 48 0.04 ± 0.01 1.21 ± 0.24 0.74 ± 0.15
96 0.07 ± 0.03 5.95 ± 1.64 5.17 ± 2.21
F4/80 48 0.25 ± 0.02 3.7 ± 0.40 2.31 ± 0.51
96 0.22 ± 0.04 3.2 ± 1.41 2.29 ± 0.72

Flow cytometry was performed on cells recovered from CG treated paws of WT and Gal-1−/− mice at 48 hours (five mice per group) and 96 hours (three mice per group). Double and single staining was carried out for Gr1/CD11b (PMN), CD11c/CCR7 (migrating DC) and F4/80 (monocyte/ MØ). Data are expressed as mean ± SEM.

P < 0.05 as compared to WT naïve (control),

P < 0.05 as compared to Gal-1−/−.