Figure 6.
Figure 6. Effect of matched increases in the concentration of plasma fibronectin present during formation of fibrin matrices and in the perfusate on platelet thrombus formation under shear conditions. (A) Fibronectin (FN), 0 to 600 μg/mL, was present during formation of fibronectin-fibrin clots. The same concentration of plasma fibronectin was included in the perfusate. After 5 minutes, perfusion at a wall shear rate of 1250 s–1 coverslips were taken out of the chamber and washed. Microscopy was performed as described in Figure 1. Bar = 100 μm. (B) Thrombus volumes (□) and platelet numbers (○) were measured as described in Table 1. Values represent the mean ± SD (n = 4 experiments). The values at fibronectin concentrations of 400 and 600 μg/mL were significantly different from values at 100 μg/mL (P < .001 in the Dunnett test after ANOVA).

Effect of matched increases in the concentration of plasma fibronectin present during formation of fibrin matrices and in the perfusate on platelet thrombus formation under shear conditions. (A) Fibronectin (FN), 0 to 600 μg/mL, was present during formation of fibronectin-fibrin clots. The same concentration of plasma fibronectin was included in the perfusate. After 5 minutes, perfusion at a wall shear rate of 1250 s–1 coverslips were taken out of the chamber and washed. Microscopy was performed as described in Figure 1. Bar = 100 μm. (B) Thrombus volumes (□) and platelet numbers (○) were measured as described in Table 1. Values represent the mean ± SD (n = 4 experiments). The values at fibronectin concentrations of 400 and 600 μg/mL were significantly different from values at 100 μg/mL (P < .001 in the Dunnett test after ANOVA).

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