Figure 5.
Figure 5. Reduced platelet adhesion and activation under flow conditions. PPACK, heparin, and fragmin anticoagulated whole blood from WT, G6b-B diY/F and G6b KO mice was flowed for 3.5 minutes (1000 s−1 shear) over coverslips coated with collagen, vWF-BP + laminin, and vWF-BP + laminin + rhodocytin. Representative brightfield images (A) and representative fluorescence images (B) following staining with Alexa Fluor 647–conjugated annexin V, P-selectin–FITC, and JON/A-PE antibodies to measure phosphatidylserine-positive platelets, α-granule release, and αIIbβ3 integrin activation (αIIbβ3act), respectively (scale bars, 10 μm). (C) Heat map showing the effect size of morphology scores and surface area coverage (SAC) of the indicated parameters, normalized to WT (n = 5 or 6).

Reduced platelet adhesion and activation under flow conditions. PPACK, heparin, and fragmin anticoagulated whole blood from WT, G6b-B diY/F and G6b KO mice was flowed for 3.5 minutes (1000 s−1 shear) over coverslips coated with collagen, vWF-BP + laminin, and vWF-BP + laminin + rhodocytin. Representative brightfield images (A) and representative fluorescence images (B) following staining with Alexa Fluor 647–conjugated annexin V, P-selectin–FITC, and JON/A-PE antibodies to measure phosphatidylserine-positive platelets, α-granule release, and αIIbβ3 integrin activation (αIIbβ3act), respectively (scale bars, 10 μm). (C) Heat map showing the effect size of morphology scores and surface area coverage (SAC) of the indicated parameters, normalized to WT (n = 5 or 6).

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