Fig. 2.
Fig. 2. Functional evaluation of the wt-A1 in flow-dependent platelet tethering. / (A) Glass coverslips coated with purified wt-A1 (300 μg/mL) were untreated (control) or treated for 30 minutes at 37°C with 1mM CuSO4 or 10 mM DTE as indicated and were perfused with platelets in reconstituted blood at a wall shear rate of 1500 seconds−1. After 3 minutes, interacting platelets were counted. Results are expressed as percentages of interacting platelets relative to the nontreated wt-A1 (*P < .01). (B) Images (205 × 330 μm) show the flow-dependent tethering of fluorescently labeled platelets on glass coverslips coated with wt-A1 (300 μg/mL) or native VWF (50 μg/mL) at 200 seconds−1(i,vi), 1000 seconds−1 (ii,vii), and 1500 seconds−1 (iii,viii) and the inhibitory effect of 30 μg/mL G19H10 (iv,ix) and 20 μg/mL AJvW-2 (v,x) at 1500 seconds−1. Corresponding platelet counts ± SDs are provided in subpanels.

Functional evaluation of the wt-A1 in flow-dependent platelet tethering.

(A) Glass coverslips coated with purified wt-A1 (300 μg/mL) were untreated (control) or treated for 30 minutes at 37°C with 1mM CuSO4 or 10 mM DTE as indicated and were perfused with platelets in reconstituted blood at a wall shear rate of 1500 seconds−1. After 3 minutes, interacting platelets were counted. Results are expressed as percentages of interacting platelets relative to the nontreated wt-A1 (*P < .01). (B) Images (205 × 330 μm) show the flow-dependent tethering of fluorescently labeled platelets on glass coverslips coated with wt-A1 (300 μg/mL) or native VWF (50 μg/mL) at 200 seconds−1(i,vi), 1000 seconds−1 (ii,vii), and 1500 seconds−1 (iii,viii) and the inhibitory effect of 30 μg/mL G19H10 (iv,ix) and 20 μg/mL AJvW-2 (v,x) at 1500 seconds−1. Corresponding platelet counts ± SDs are provided in subpanels.

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