Figure 4.
Figure 4. Static platelet adhesion to extracellular matrices. Anticoagulated whole blood from CD151+/+ and CD151–/– mice was labeled with DiOC6 (50 μg/mL) and washed platelets were isolated. Labeled platelets/mL (1 × 109 platelets/μL) were then allowed to adhere to collagen-coated (2.5 mg/mL), fibrinogen-coated (100 μg/mL), or bovine VWF–coated (20 μg/mL) coverslips in the presence of botrocetin (1 μg/mL) for 15 to 60 minutes at 37° C. Adherent platelets were fixed at different time points and visualized using fluorescence microscopy. Quantitation of adherent CD151+/+ and CD151–/– platelets was determined by analysis of images acquired using × 100 objective. These data represent the mean ± SEM from 3 independent experiments. HPF indicates high power field.

Static platelet adhesion to extracellular matrices. Anticoagulated whole blood from CD151+/+ and CD151–/– mice was labeled with DiOC6 (50 μg/mL) and washed platelets were isolated. Labeled platelets/mL (1 × 109 platelets/μL) were then allowed to adhere to collagen-coated (2.5 mg/mL), fibrinogen-coated (100 μg/mL), or bovine VWF–coated (20 μg/mL) coverslips in the presence of botrocetin (1 μg/mL) for 15 to 60 minutes at 37° C. Adherent platelets were fixed at different time points and visualized using fluorescence microscopy. Quantitation of adherent CD151+/+ and CD151–/– platelets was determined by analysis of images acquired using × 100 objective. These data represent the mean ± SEM from 3 independent experiments. HPF indicates high power field.

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