Figure 3
Figure 3. In vitro thrombogenesis on collagen surface under flow. (A) Thrombus formation at 1000 s−1. Whole blood from Adamts13L/L, Adamts13S/S, or Adamts13−/− mice containing mepacrine-labeled platelets was perfused over an acid-insoluble type I collagen–coated surface at a wall shear rate of 1000 s−1. The cumulative thrombus volume, analyzed using a multidimensional imaging system, was measured every 0.5 minutes until 4 minutes. Data are the mean ± SEM of 25 mice for each genotype. (B) Thrombus formation at 5000 s−1. Whole-blood samples from indicated mice were perfused over an acid-insoluble type I collagen–coated surface at a wall shear rate of 5000 s−1. The cumulative thrombus volume was measured every 20 seconds until 80 seconds. Blood from 2 mice was pooled and used for experiments. Data are the mean ± SEM of 15 samples for each genotype. *P < .05 in comparison with Adamts13L/L mice.

In vitro thrombogenesis on collagen surface under flow. (A) Thrombus formation at 1000 s−1. Whole blood from Adamts13L/L, Adamts13S/S, or Adamts13−/− mice containing mepacrine-labeled platelets was perfused over an acid-insoluble type I collagen–coated surface at a wall shear rate of 1000 s−1. The cumulative thrombus volume, analyzed using a multidimensional imaging system, was measured every 0.5 minutes until 4 minutes. Data are the mean ± SEM of 25 mice for each genotype. (B) Thrombus formation at 5000 s−1. Whole-blood samples from indicated mice were perfused over an acid-insoluble type I collagen–coated surface at a wall shear rate of 5000 s−1. The cumulative thrombus volume was measured every 20 seconds until 80 seconds. Blood from 2 mice was pooled and used for experiments. Data are the mean ± SEM of 15 samples for each genotype. *P < .05 in comparison with Adamts13L/L mice.

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