Figure 6.
Figure 6. Activation-independent platelet aggregation mediated by multimeric VWF or isolated VWF A1 domain. Perfusion over immobilized VWF of washed blood cells suspended in Hepes/Tyrode buffer, pH 7.4 (see legend to Figure 2B). In the presence of soluble multimeric VWF (+VWF; 20 μg/mL), single platelets adhere when the shear rate is 2500 s–1, and elongated, firmly adherent activation-independent aggregates form at 23 000 s–1. In contrast, in the presence of soluble dimeric VWF A1 domain (+dA1; 5 μg/mL), large rolling aggregates form on the surface when the shear rate is 2500 s–1, but only single platelets adhere when the shear rate is 23 000 s–1. Bar graph: Quantitative evaluation of the number of activation-independent aggregates with cross-sectional area more than 100 μM2 present at positions exposed to the indicated wall shear rates in the presence of soluble VWF (VWF multimers) or isolated dimeric A1 domain (dVWFA1). Measurements performed in a field of view = 120 000 μM2. Images from Video S10.

Activation-independent platelet aggregation mediated by multimeric VWF or isolated VWF A1 domain. Perfusion over immobilized VWF of washed blood cells suspended in Hepes/Tyrode buffer, pH 7.4 (see legend to Figure 2B). In the presence of soluble multimeric VWF (+VWF; 20 μg/mL), single platelets adhere when the shear rate is 2500 s–1, and elongated, firmly adherent activation-independent aggregates form at 23 000 s–1. In contrast, in the presence of soluble dimeric VWF A1 domain (+dA1; 5 μg/mL), large rolling aggregates form on the surface when the shear rate is 2500 s–1, but only single platelets adhere when the shear rate is 23 000 s–1. Bar graph: Quantitative evaluation of the number of activation-independent aggregates with cross-sectional area more than 100 μM2 present at positions exposed to the indicated wall shear rates in the presence of soluble VWF (VWF multimers) or isolated dimeric A1 domain (dVWFA1). Measurements performed in a field of view = 120 000 μM2. Images from Video S10.

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