Summary
Anticoagulant plasma protein S (PS) is essential for maintaining haemostatic balance.
About 2.5% of PS is stored in platelets and released upon platelet stimulation. So
far, little is known about the functionality and importance of platelet (plt)PS. A
platelet-associated protease cleaves plasma-derived (pd)PS and pltPS in the “thrombin-sensitive
region”, abolishing activated protein C (APC) cofactor activity. However, we showed
that cleaved PS retains APC-independent anticoagulant activities (“PS-direct”). To
investigate whether pltPS or pdPS exert PS-direct on platelets or platelet-shed microparticles,
thrombin and factor (F)Xa generation on unstimulated or stimulated washed platelets
and microparticles were measured. Western blotting revealed that pltPS and pdPS bound
to washed, stimulated platelets and microparticles, and that pltPS had slower electrophoretic
mobility than pdPS. Platelet stimulation in the presence of inhibitory anti-PS antibodies
resulted in 2.6 ± 1.6-fold (p<0.0004, n=20) more thrombin generation upon addition
of FXa and prothrombin. PltPS exerted PSdirect that was similar to or greater than
that of Zn2+-containing pdPS and much greater than that of Zn2+-deficient pdPS. Findings were confirmed using purified pltPS. Platelet-bound pltPS
and microparticlebound pltPS had similar PS-direct. Finally, platelet stimulation
in the presence of inhibitory anti-PS antibodies resulted in 1.5 ± 0.2-fold (p<0.0001,
n=11) more FXa generation upon addition of TF/FVIIa and FX. Thus, pltPS inhibits both
prothrombinase and extrinsic FXase activities. Neutralising antibodies against APC
and TFPI had no effect on the PS-direct of pltPS or pdPS on platelets. This study
indicates that pltPS may be an essential pool of PS that counterbalances procoagulant
activities on platelets.
Keywords
Activated protein C - protein S - platelets - microparticles - anticoagulant activity