Functional Significance of Adenosine 5 -Diphosphate Receptor (P2Y12) in Platelet Activation Initiated by Binding of von Willebrand Factor to Platelet GP Ib Induced by Conditions of High Shear Rate
نویسندگان
چکیده
Background—The role of the adenosine 5 -diphosphate receptor P2Y12 in platelet activation initiated by the von Willebrand factor (VWF)–GP Ib interaction under high shear rate was investigated. Methods and Results—Blood samples were obtained from 11 donors. Shear-induced platelet aggregation was detected by optically modified cone-plate viscometer. Shear-induced VWF binding, P-selectin expression, and microparticle release were detected by flow cytometry. Platelet interaction with immobilized VWF was also investigated by parallel-plate flow chamber equipped with epifluorescent videomicroscopy. Effects of a selective P2Y12 antagonist AR-C69931 MX were tested. AR-C69931 MX inhibited shear-induced platelet aggregation in a dose-dependent manner, achieving the maximum inhibition at 100 nmol/L. The extent of aggregation after exposure to a shear rate of 10 800 s 1 for 6 minutes in the presence of 100 nmol/L AR-C69931 MX was 32.4 8.2% (mean SD), which was significantly lower than the value in the controls of 69.7 9.6% (P 0.01). The inhibiting effects of AR-C69931 MX were reversed by exogenous addition of adenosine 5 -diphosphate. Shear-induced VWF binding and P-selectin surface translocation, which occurred in 4696 911 and 5964 784, respectively, of 10 000 measured platelets, was also inhibited by AR-C69931 MX (100 nmol/L) to 1948 528 and 2797 718, respectively (P 0.0018 and P 0.0009). Microparticle release was similarly inhibited. In a flow chamber experiment, firm platelet attachment on immobilized VWF was inhibited by AR-C69931 MX, whereas transient interaction was not influenced. All the above reactions were completely inhibited by blocking VWF–GP Ib interaction. Conclusions—We have demonstrated that the stimulation of P2Y12 is involved in platelet activation initiated by the binding of VWF to GP Ib induced by a high shear rate. (Circulation. 2002;105:2531-2536.)
منابع مشابه
Epinephrine augments von Willebrand factor-dependent shear-induced platelet aggregation.
BACKGROUND Shear-induced platelet aggregation (SIPA) is an important mechanism in thrombogenesis. von Willebrand factor (vWF) binding to platelet glycoprotein Ib (GP Ib) has been found to be crucial for platelet aggregation under the high shear force probably generated in stenosed coronary artery. The physiological significance of vWF-dependent SIPA has not been clarified. METHODS AND RESULTS...
متن کاملRistocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions.
Under conditions of high shear stress, both hemostasis and thrombosis are initiated by the interaction of the platelet membrane glycoprotein (GP) Ib-IX-V complex with its adhesive ligand, von Willebrand factor (vWF), in the subendothelial matrix or plasma. This interaction involves the A1 domain of vWF and the N-terminal extracellular region of GP Ibalpha (His-1-Glu-282), and it can also be ind...
متن کاملLocalization of the Adhesion Receptor Glycoprotein Ib-IX-V Complex to Lipid Rafts Is Required for Platelet Adhesion and Activation
The platelet glycoprotein (GP) Ib-IX-V complex mediates the attachment of platelets to the blood vessel wall by binding von Willebrand factor (VWF), an interaction that also transmits signals for platelet activation and aggregation. Because the complex is extensively palmitoylated, a modification known to target proteins to lipid rafts, we investigated the role of raft localization in GP Ib-IX-...
متن کاملHEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY Blockade of adenosine diphosphate receptors P2Y12 and P2Y1 is required to inhibit platelet aggregation in whole blood under flow
Using heparinized whole blood and flow conditions, it was shown that adenosine 5*-diphosphate (ADP) receptors P2Y12 and P2Y1 are both important in direct shearinduced platelet aggregation and platelet aggregation subsequent to initial adhesion onto von Willebrand factor (vWf)– collagen. In the viscometer, whole blood was subjected to shear rates of 750, 1500, and 3000 s21 for 30 seconds at room...
متن کاملHEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions
Under conditions of high shear stress, both hemostasis and thrombosis are initiated by the interaction of the platelet membrane glycoprotein (GP) Ib-IX-V complex with its adhesive ligand, von Willebrand factor (vWF), in the subendothelial matrix or plasma. This interaction involves the A1 domain of vWF and the N-terminal extracellular region of GP Iba (His-1-Glu-282), and it can also be induced...
متن کامل