Fig. 7.
Effects of thrombin, HLE, Cat G, and PR3 on the expression of the thrombin receptor at the surface of platelets. Unstirred platelets were incubated for 5 minutes with thrombin (A) or the neutrophil proteinases (B to D) as described in the legend to Fig 6. Binding of the IIaR-A antibody was measured by flow cytometry as detailed in the legend to Fig 5. For each experimental condition, the observed tracing (in black) is shown for comparison with a typical tracing (superimposed) representative of the control condition (ie, without pretreatment with any of the proteinases). The MFI value for the control irrelevant monoclonal IgG was 15.2 ± 2.1 (n = 10). Tracings are representative of at least three distinct experiments.

Effects of thrombin, HLE, Cat G, and PR3 on the expression of the thrombin receptor at the surface of platelets. Unstirred platelets were incubated for 5 minutes with thrombin (A) or the neutrophil proteinases (B to D) as described in the legend to Fig 6. Binding of the IIaR-A antibody was measured by flow cytometry as detailed in the legend to Fig 5. For each experimental condition, the observed tracing (in black) is shown for comparison with a typical tracing (superimposed) representative of the control condition (ie, without pretreatment with any of the proteinases). The MFI value for the control irrelevant monoclonal IgG was 15.2 ± 2.1 (n = 10). Tracings are representative of at least three distinct experiments.

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