Figure 1.
Figure 1. The formation of ULVWF–platelet strings under flow condition was blocked by anti–P-selectin antibody or soluble P-selectin. HUVECs were stimulated with histamine in the absence or presence of a polycloncal anti–P-selectin antibody, purified human P-selectin, the monoclonal anti-αvβ3 antibody LMP609, RGDS peptide, or heparin for 15 minutes at room temperature. Washed platelets suspended in Ca++, Mg++-free Tyrode buffer were then perfused over the stimulated endothelial cells at 2.5 dyn/cm2 for 2 minutes at 37°C. The number of ULVWF–platelets strings was then counted in 20 continuous fields of 400 × (A, bar = 100 μm). Results in (D) are from 12 separate experiments. Data are mean ± SEM.

The formation of ULVWF–platelet strings under flow condition was blocked by anti–P-selectin antibody or soluble P-selectin. HUVECs were stimulated with histamine in the absence or presence of a polycloncal anti–P-selectin antibody, purified human P-selectin, the monoclonal anti-αvβ3 antibody LMP609, RGDS peptide, or heparin for 15 minutes at room temperature. Washed platelets suspended in Ca++, Mg++-free Tyrode buffer were then perfused over the stimulated endothelial cells at 2.5 dyn/cm2 for 2 minutes at 37°C. The number of ULVWF–platelets strings was then counted in 20 continuous fields of 400 × (A, bar = 100 μm). Results in (D) are from 12 separate experiments. Data are mean ± SEM.

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