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Arterioscler Thromb Vasc Biol. 2010 Dec;30(12):2400-7. doi: 10.1161/ATVBAHA.110.216531. Epub 2010 Nov 11.

Properties of procoagulant platelets: defining and characterizing the subpopulation binding a functional prothrombinase.

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  • 1Department of Biochemistry, University of Vermont College of Medicine, Burlington, Vt 05405, USA.

Abstract

OBJECTIVE:

The goal of this study was to define and characterize the subpopulation of platelets capable of regulating the functional interactions of factors Va (FVa) and Xa (FXa) on the thrombin-activated platelet surface.

METHODS AND RESULTS:

Flow cytometric analyses were used to define and characterize platelet subpopulations. At a concentration of thrombin known to elicit maximal platelet activation, platelet-derived FVa release, and prothrombinase assembly/function, only a subpopulation of platelets was positive for FVa and FXa binding. An additional subpopulation bound lower levels of FVa but little, if any, FXa. Fluorescence microscopy analyses confirmed these data. Phenotypically, platelets capable of binding FXa were more highly reticulated and demonstrated significantly increased expression of several key adhesion molecules, including P-selectin, glycoprotein Ibα, and integrins α(IIb) and β(3). This platelet subpopulation was also defined by the expression of a nondissociable, membrane-bound pool of functional platelet-derived FVa, which made up ≈35% to 50% of the total membrane-bound cofactor.

CONCLUSIONS:

The ability of activated platelets to support thrombin generation is defined by a subpopulation of platelets expressing a nondissociable pool of platelet-derived FVa and increased adhesive receptor density. This subpopulation is hypothesized to play a significant role in regulating both normal hemostasis and pathological thrombus formation because the adherent properties of platelets and their ability to mount and sustain a procoagulant response are crucial steps in both of these processes.

PMID:
21071689
[PubMed - indexed for MEDLINE]
PMCID:
PMC3156579
Free PMC Article

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