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. 2003 Mar;108(3):352–364. doi: 10.1046/j.1365-2567.2003.01609.x

Figure 1.

Figure 1

Recruitment of CD11c+ F4/80+ CD11b (AM), CD11c F4/80+ CD11b+ (IM) and CD11c+ F4/80 CD11b (DC) to the lungs of mice shortly after i.n. delivery of BCG. Cells harvested from the BAL and from digested lung tissue 6–96 hr after i.n. delivery of BCG (106 CFU) were stained with antibodies as follows: FITC- or PE-conjugated CD11c, F4/80 and CD11b. Cells expressing CD11c+ F4/80+ CD11b (AM) or CD11c F4/80+ CD11b+ (IM) or CD11c+ F4/80 CD11b (DC) were analysed by FACScan flow cytometry. Rat IgG2a, rat IgG2b isotypes and hamster IgG were used as controls. The number of cells present in the three populations was calculated as: percentage of each subset as determined by FACS analysis × number of cells counted in the BAL or lung digest, and was expressed as the mean ± SEM. Values of P < 0·05 (*) were considered significant. The results shown are representative of three separate experiments.