Table 1.

Thrombin Generation by Apoptotic VSMCs and Platelets

No. of ExperimentsAUC (nmol⋅min/L)Peak Thrombin (nmol/L)
Buffer C 43.8 ± 3.4* 26.3 ± 2.5* 
Platelets 14 220.8 ± 14.8* 98.6 ± 7.4* 
Activated platelets 15 331.5 ± 15.1 172.5 ± 7.8 
Apoptotic VSMC-myc cells (2.24 × 109/L) 304.6 ± 16.9 154.5 ± 9.0 
Apoptotic VSMC-myc cells (1.32 × 109/L) 267.0 ± 5.4 130.9 ± 11.1 
Apoptotic VSMC-myc cells (0.73 × 109/L) 170.0 ± 3.2 75.8 ± 1.0 
Apoptotic VSMC-myc cells (0.11 × 109/L) 90.4 ± 0.4 39.2 ± 0.7 
Apoptotic human E1A cells 211.0 ± 8.5 102.8 ± 4.1 
No. of ExperimentsAUC (nmol⋅min/L)Peak Thrombin (nmol/L)
Buffer C 43.8 ± 3.4* 26.3 ± 2.5* 
Platelets 14 220.8 ± 14.8* 98.6 ± 7.4* 
Activated platelets 15 331.5 ± 15.1 172.5 ± 7.8 
Apoptotic VSMC-myc cells (2.24 × 109/L) 304.6 ± 16.9 154.5 ± 9.0 
Apoptotic VSMC-myc cells (1.32 × 109/L) 267.0 ± 5.4 130.9 ± 11.1 
Apoptotic VSMC-myc cells (0.73 × 109/L) 170.0 ± 3.2 75.8 ± 1.0 
Apoptotic VSMC-myc cells (0.11 × 109/L) 90.4 ± 0.4 39.2 ± 0.7 
Apoptotic human E1A cells 211.0 ± 8.5 102.8 ± 4.1 

Apoptotis was induced by serum starvation of rat VSMCs expressing c-myc or normal human coronary VSMCs expressing the adenovirus gene E1A. Apoptotic cells were suspended to give an assay concentration of 2.24 × 109/L (except where otherwise stated), giving approximately the same surface area as 50 × 109/L unactivated or calcium-ionophore–activated platelets. Defibrinated plasma was activated with Russel's Viper Venom, and the thrombin generated after the addition of platelets or apoptotic VSMCs was measured in a chromogenic assay. The table shows the area under the thrombin generation curves (AUC) and the peak thrombin concentration. Values are mean ± SEM.

*

P < .005 compared with apoptotic VSMC-myc cells.

P = not significant compared with apoptotic VSMC-myc cells.

P < .0001 compared with buffer C.

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