%0 Journal Article %A Schroder, Wayne A %A Le, Thuy T %A Gardner, Joy %A K. Andrews, Robert %A E. Gardiner, Elizabeth %A Callaway, Leonie %A Suhrbier, Andreas %D 2018 %T SerpinB2 deficiency in mice reduces bleeding times via dysregulated platelet activation %U https://tandf.figshare.com/articles/journal_contribution/SerpinB2_deficiency_in_mice_reduces_bleeding_times_via_dysregulated_platelet_activation/7294394 %R 10.6084/m9.figshare.7294394.v1 %2 https://tandf.figshare.com/ndownloader/files/13475072 %K Bleeding times %K PAI-2 %K plasminogen activation inhibitor type 2 %K platelet %K SerpinB2 %K urokinase %X

SerpinB2, also known as plasminogen activation inhibitor type 2 (PAI-2), is classically viewed as an inhibitor of fibrinolysis. However, we show herein a distinct, hitherto unrecognized role for SerpinB2 in hemostasis. Mice deficient in SerpinB2 expression and mice with an active site mutation in SerpinB2, both showed significant reductions in tail bleeding times. This hemostatic phenotype was associated with platelets, with SerpinB2 and SerpinB2-urokinase complexes clearly present in platelet fractions, and immunohistochemistry of blood clots suggesting SerpinB2 is associated with platelet aggregates. Thromboelastography illustrated faster onset of clot formation in blood from SerpinB2 deficient mice, whereas clotting of platelet-free plasma was unaffected. The results appear consistent with the low circulating SerpinB2 levels and hypercoagulation seen during pre-eclampsia; however, SerpinB2 was not detected in human platelets.

%I Taylor & Francis