Figure 4
Figure 4. The p75 TNF-α receptor is essential for TNF-α–induced firm adhesion. (A) Representative leukocyte firm adhesion profile following mouse TNF-α treatment of WT (○), p75−/− (▪), p55−/− (▴), and D−/− (□) mice. One hour after surgery, TNF-α (2 ng/mL in 25 μL) was applied directly to a 25-mm2 area of the cremaster muscle flap. Number of adhering leukocytes was counted in a time window of 2 minutes in a 100-μm viewing segment. Control counts were obtained prior to TNF-α application. (B) Average fold change with respect to control in early- and late-phase firm adhesion of leukocytes upon TNF-α treatment of WT (filled bar), p75−/− (spotted bar), p55−/− (hatched bar), and D−/− (shaded bar) cremasters. Group size equals 4, error bars represent SD, the asterisk indicates statistical significance (P < .05).

The p75 TNF-α receptor is essential for TNF-α–induced firm adhesion. (A) Representative leukocyte firm adhesion profile following mouse TNF-α treatment of WT (○), p75−/− (▪), p55−/− (▴), and D−/− (□) mice. One hour after surgery, TNF-α (2 ng/mL in 25 μL) was applied directly to a 25-mm2 area of the cremaster muscle flap. Number of adhering leukocytes was counted in a time window of 2 minutes in a 100-μm viewing segment. Control counts were obtained prior to TNF-α application. (B) Average fold change with respect to control in early- and late-phase firm adhesion of leukocytes upon TNF-α treatment of WT (filled bar), p75−/− (spotted bar), p55−/− (hatched bar), and D−/− (shaded bar) cremasters. Group size equals 4, error bars represent SD, the asterisk indicates statistical significance (P < .05).

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