Figure 1.
Figure 1. α2 integrin–deficient mice display a diminished PMN response to Listeria infection. (A) Wild-type (WT) and α2 integrin–deficient (KO) mice were infected with 5 × 104 Listeria intraperitoneally. At indicated times after infection, the absolute peritoneal PMN number was determined. Shown is the combination of 3 experiments (mean ± SEM), with each point representing 4-8 mice. P = .046 at 6 hours after infection. (B) WT and KO mice were injected with thioglycollate intraperitoneally. At indicated times after injection, the absolute peritoneal PMN number was determined. Shown is the combination of 3 experiments (mean ± SEM), with each point representing 5-6 mice (time 0 hours, 3-4 mice). (C,D) Representative cytospin preparations of peritoneal exudates at 6 hours after Listeria infection from (C) wild-type and (D) α2 integrin–deficient mice.

α2 integrin–deficient mice display a diminished PMN response to Listeria infection. (A) Wild-type (WT) and α2 integrin–deficient (KO) mice were infected with 5 × 104Listeria intraperitoneally. At indicated times after infection, the absolute peritoneal PMN number was determined. Shown is the combination of 3 experiments (mean ± SEM), with each point representing 4-8 mice. P = .046 at 6 hours after infection. (B) WT and KO mice were injected with thioglycollate intraperitoneally. At indicated times after injection, the absolute peritoneal PMN number was determined. Shown is the combination of 3 experiments (mean ± SEM), with each point representing 5-6 mice (time 0 hours, 3-4 mice). (C,D) Representative cytospin preparations of peritoneal exudates at 6 hours after Listeria infection from (C) wild-type and (D) α2 integrin–deficient mice.

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