Fig. 9.
Fig. 9. Effect of RhoA inactivation by C3 exoenzyme on fibrin clot retraction. Washed platelets were incubated for 4 hours at 37°C with vehicle buffer (“No C3”) or 400 μg/mL of C3. Alternatively, platelets were incubated for 3 hours, 50 minutes without additive, and then with DMSO or 10 μmol/L cytochalasin D (Cyto D) for 10 minutes. Then platelets were added to citrated plasma in siliconized glass tubes, and clotting was initiated with 8 U/mL of thrombin and 2 mmol/L CaCl2. After 90 minutes at 37°C, clot retraction was quantitated as described in Materials and Methods. Data represent the means of three experiments. Error bars have been omitted for clarity.

Effect of RhoA inactivation by C3 exoenzyme on fibrin clot retraction. Washed platelets were incubated for 4 hours at 37°C with vehicle buffer (“No C3”) or 400 μg/mL of C3. Alternatively, platelets were incubated for 3 hours, 50 minutes without additive, and then with DMSO or 10 μmol/L cytochalasin D (Cyto D) for 10 minutes. Then platelets were added to citrated plasma in siliconized glass tubes, and clotting was initiated with 8 U/mL of thrombin and 2 mmol/L CaCl2. After 90 minutes at 37°C, clot retraction was quantitated as described in Materials and Methods. Data represent the means of three experiments. Error bars have been omitted for clarity.

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