Mechanisms of thrombin inhibition by protein S and the TFPIα-fVshort-protein S complex.

Protein S (PS) is an important anticoagulant implicated in both bleeding and thrombotic disorders, making it a promising drug target. The anticoagulant function of PS arises in part because PS enhances the anticoagulant function of tissue factor pathway inhibitor α (TFPIα). PS has been proposed to circulate in the bloodstream together with TFPIα and a truncated form of factor V (fV-short) in the trimolecular complex, TFPIα-PS-fV-short, which we call protein S complex (PSC). PSC has been proposed to strongly inhibit thrombin production by enhancing the ability of TFPIα to inhibit clotting factor Xa up to 100-fold and by localizing to platelet membranes, limiting fXa activity shortly after coagulation starts. Yet, exactly how PS functions with TFPIα as an anticoagulant remains poorly understood. To investigate, we extend an experimentally validated mathematical model of blood coagulation to include PSC and free PS (not a part of PSC) in the plasma, as well as free PS and TFPIα in platelets. We find that shortly after coagulation initiation, PSC strongly inhibits thrombin production. We find that the (unknown) magnitude of the enhanced affinity of PSC binding to inhibit fXa critically regulates PSC's impact on thrombin production. We find that, under flow, PSC can accumulate on platelets to concentrations ∼50 times higher than in the plasma, previously unreported to our knowledge. We also find that PSC limits thrombin production by occupying fV-specific binding sites on platelets. Our results show that changes in PSC can dramatically impact severity of pathological bleeding disorders. For the east Texas bleeding disorder, elevated PSC concentrations eliminate thrombin bursts, leading to bleeding. With fV deficiency, reducing PSC rescues thrombin production in severe fV deficiency and returns thrombin production due to mild fV deficiency to normal. Finally, thrombin production in severe hemophilia A can be substantially improved by blocking PSC's anticoagulant function.