Key result
Recombinant tick protein TIX-5 inhibits FXa-mediated factor V activation to halt early coagulation.
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Demonstrates that FXa-mediated activation of factor V is a crucial physiological event in the initiation phase of blood coagulation, challenging the dogma that thrombin is the sole initial activator.
BACKGROUND: Generation of active procoagulant cofactor factor Va (FVa) and its subsequent association with the enzyme activated factor X (FXa) to form the prothrombinase complex is a pivotal initial event in blood coagulation and has been the subject of investigative effort, speculation, and controversy. The current paradigm assumes that FV activation is initiated by limited proteolysis by traces of (meizo) thrombin. METHODS AND RESULTS: Recombinant tick salivary protein TIX-5 was produced and anticoagulant properties were studied with the use of plasma, whole blood, and purified systems. Here, we report that TIX-5 specifically inhibits FXa-mediated FV activation involving the B domain of FV and show that FXa activation of FV is pivotal for plasma and blood clotting. Accordingly, tick feeding is impaired on TIX-5 immune rabbits, displaying the in vivo importance of TIX-5. CONCLUSIONS: Our data elucidate a unique molecular mechanism by which ticks inhibit the host's coagulation system. From our data, we propose a revised blood coagulation scheme in which direct FXa-mediated FV activation occurs in the initiation phase during which thrombin-mediated FV activation is restrained by fibrinogen and inhibitors.
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Schuijt et al. (2013) studied Blood coagulation. Recombinant tick salivary protein TIX-5 vs. Control (PBS, rP19, or absence of TIX-5) was evaluated on Inhibition of FXa-mediated FV activation and thrombin generation. Recombinant tick salivary protein TIX-5 specifically inhibited FXa-mediated factor V activation, demonstrating that direct FXa-mediated FV activation is pivotal for the initiation of blood coagulation.
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