Figure 6.
Figure 6. MCP-1 is critical for early monocyte recruitment and is unaffected by deficient neutrophil recruitment. (A) Time course of cell migration in MCP-1+/+ (•) and MCP-1-/- (▴) mice; MCP-1+/+ and MCP-1-/- infiltrating cells were compared at each time point (*P ≤ .05). (B) Reduced neutrophil infiltration in LFA-1-/- () compared with LFA-1+/+ (□) mice, and further reduction with anti-α4 mAb PS2/3, LFA-1+/+, and LFA-1-/- infiltrating cells were compared at each time point (*P ≤ .001). (C) MCP-1 levels in peritoneal lavage of mice (panel B) with blocked neutrophil migration; LFA-1+/+ and LFA-1-/- lavages were compared at each time point (P ≥ .05 for all time points). Data shown are representative of 2 or more experiments (means of 4-5 mice per group ±, SEM).

MCP-1 is critical for early monocyte recruitment and is unaffected by deficient neutrophil recruitment. (A) Time course of cell migration in MCP-1+/+ (•) and MCP-1-/- (▴) mice; MCP-1+/+ and MCP-1-/- infiltrating cells were compared at each time point (*P ≤ .05). (B) Reduced neutrophil infiltration in LFA-1-/- () compared with LFA-1+/+ (□) mice, and further reduction with anti-α4 mAb PS2/3, LFA-1+/+, and LFA-1-/- infiltrating cells were compared at each time point (*P ≤ .001). (C) MCP-1 levels in peritoneal lavage of mice (panel B) with blocked neutrophil migration; LFA-1+/+ and LFA-1-/- lavages were compared at each time point (P ≥ .05 for all time points). Data shown are representative of 2 or more experiments (means of 4-5 mice per group ±, SEM).

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