Table 1.

Expression of microparticle-associated tissue factor procoagulant activity on in vitro-generated microparticles


Cellular origin of MPs

MP-associated TF PCA in supernatant [Xa], pM/h per 106 cells
Fibroblasts  
Ionophore  > 300  
Ionophore+  > 300  
Smooth muscle cells  
Ionophore  > 300  
Ionophore+  > 300  
HUVECs  
TNF  4  
TNF+  26  
CD14+ monocytes  
LPS  3  
LPS+  20  
Platelets  
Ionophore  0  
Ionophore+  0  
Red blood cells  
Ionophore  0  
Ionophore+
 
1
 

Cellular origin of MPs

MP-associated TF PCA in supernatant [Xa], pM/h per 106 cells
Fibroblasts  
Ionophore  > 300  
Ionophore+  > 300  
Smooth muscle cells  
Ionophore  > 300  
Ionophore+  > 300  
HUVECs  
TNF  4  
TNF+  26  
CD14+ monocytes  
LPS  3  
LPS+  20  
Platelets  
Ionophore  0  
Ionophore+  0  
Red blood cells  
Ionophore  0  
Ionophore+
 
1
 

Cells were isolated as described in “Materials and methods.” Fibroblasts, smooth muscle cells, red blood cells, and platelets (106 cells in each case) were activated by exposure to 10 μM ionophore (or vehicle control) for 10 minutes at 37°C. Monocytes were activated by exposure to 10 ng/mL LPS (or vehicle control) for 4 hours at 37°C and HUVECs were activated by exposure to 10 ng/mL TNF-α (or vehicle control) for 4 hours at 37°C. In every case, the supernatant was removed and assayed for MP-associated TF PCA as described in “Materials and methods.”

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