Figure 4.
Preexposure to NS1 amplifies platelet activation by suboptimal concentrations of procoagulant agonists. Platelets were stimulated with NS1 (0, 0.5, or 5 µg/mL) produced in SF9 cells for 2.5 hours and restimulated with thrombin (0.05 U/mL), PAF (40 nM), oxLDL (5 µg/mL), epinephrine (10 µM), or ATP (2mM) for 30 minutes. (A) The percentage of platelets expressing surface P-selectin (CD62P); and the concentrations of MIF (B) and TXB2 (C) in platelet supernatants were evaluated. (D) Platelets were pretreated for 30 minutes with aspirin (100 μM) or vehicle, stimulated for 2.5 hours with 5 µg/mL of NS1 produced in SF9 cells, and restimulated for 30 minutes with thrombin (0.05 U/mL) or PAF (40 nM). The percentage of platelets expressing surface P-selectin was evaluated. Bars represent mean ± standard error of the mean of 5 independent experiments. *P < .05 compared with unstimulated platelets; #P < .05 compared with procoagulant agonists or NS1 alone.

Preexposure to NS1 amplifies platelet activation by suboptimal concentrations of procoagulant agonists. Platelets were stimulated with NS1 (0, 0.5, or 5 µg/mL) produced in SF9 cells for 2.5 hours and restimulated with thrombin (0.05 U/mL), PAF (40 nM), oxLDL (5 µg/mL), epinephrine (10 µM), or ATP (2mM) for 30 minutes. (A) The percentage of platelets expressing surface P-selectin (CD62P); and the concentrations of MIF (B) and TXB2 (C) in platelet supernatants were evaluated. (D) Platelets were pretreated for 30 minutes with aspirin (100 μM) or vehicle, stimulated for 2.5 hours with 5 µg/mL of NS1 produced in SF9 cells, and restimulated for 30 minutes with thrombin (0.05 U/mL) or PAF (40 nM). The percentage of platelets expressing surface P-selectin was evaluated. Bars represent mean ± standard error of the mean of 5 independent experiments. *P < .05 compared with unstimulated platelets; #P < .05 compared with procoagulant agonists or NS1 alone.

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