To cite this article: Butenas S, Dee JD, Mann KG. The function of factor XI in tissue factor-initiated thrombin generation. J Thromb Haemost 2003;See also Walsh PN. Roles of Factor XI, platelets and tissue factor-initiated blood coagulation. This issue, pp. 2081±6.Summary. The in¯uence of plasma and platelet factor (F)XI on thrombin generation initiated with 10 pM tissue factor (TF) in a synthetic coagulation model was evaluated in the presence of either 2 Â 10 8 mL À1 platelets or the equivalent (2 mM) phospholipids. In either system, with all proteins present at physiological concentrations, FXI (30 nM) had no effect on thrombin generation. With phospholipids in the absence of FXI, an increase in vitamin K-dependent proteins (VKDP) (up to 500%) signi®-cantly prolonged the initiation phase of thrombin generation and decreased maximum thrombin levels. The inhibition was principally caused by the elevated prothrombin and FIX concentrations. When 30 nM FXI was added with elevated VKDP and phospholipids, the initiation phase was decreased and the maximum thrombin levels generated substantially increased. In experiments with platelets (with and without plasma FXI), an increase in VKDP had little effect on the initiation phase of thrombin generation. These data indicate that (i) FXI has no effect on thrombin generation at 10 pM TF and physiological concentrations of VKDP; (ii) platelets and plasma FXI are able to compensate for the inhibitory effects of elevated VKDP.

FDPOs enhanced wound healing in db/db mice as well as FDPIs and RT-PLTs. Wound closure was obtained 6 days earlier than untreated wounds and histologic examination revealed reduced granulation and increased cellular angiogenesis.