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二磷酸腺苷四磷酸(血小板致密颗粒的组成部分)对血小板 P2Y1、P2Y12 和 P2X1 受体的激动剂和拮抗剂作用。

Agonist and antagonist effects of diadenosine tetraphosphate, a platelet dense granule constituent, on platelet P2Y1, P2Y12 and P2X1 receptors.

机构信息

Center for Platelet Function Studies, Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

Thromb Res. 2010 Feb;125(2):159-65. doi: 10.1016/j.thromres.2009.11.006. Epub 2009 Nov 27.

Abstract

INTRODUCTION

Diadenosine 5',5'''-P(1),P(4)- tetraphosphate (Ap(4)A) is stored in platelet dense granules, but its effects on platelet function are not well understood.

METHODS AND RESULTS

We examined the effects of Ap(4)A on platelet purinergic receptors P2Y(1), P2Y(12) and P2X(1). Flow cytometry was used to measure the effects of Ap(4)A in the presence or absence of ADP on: a) P2Y(12)-mediated decrease in intraplatelet phosphorylated vasodilator stimulated phosphoprotein (VASP), b) P2Y(1)-mediated increase in platelet cytosolic Ca(2+), and c) P2X(1)-mediated intraplatelet entry of extracellular Ca(2+). ADP-stimulated platelet shape change (P2Y(1)-mediated) and aggregation (P2Y(1)- and P2Y(12)-mediated) were measured optically. Ap(4)A inhibited 3 microM ADP-induced: a) platelet aggregation (IC(50) 9.8+/-2.8 microM), b) P2Y(1)-mediated shape change, c) P2Y(1)-mediated increase in platelet cytosolic Ca(2+) (IC(50) 40.8+/-12.3 microM), and d) P2Y(12)-mediated decrease in VASP phosphorylation (IC(50)>250 microM). In the absence of added ADP, Ap(4)A had agonist effects on platelet P2X(1) and P2Y(12), but not P2Y(1), receptors.

CONCLUSION

Ap(4)A, a constituent of platelet dense granules, is a) an antagonist of platelet P2Y(1) and P2Y(12) receptors, where it inhibits the effects of ADP, and b) an agonist of platelet P2X(1) and P2Y(12) receptors.

摘要

简介

二腺苷 5',5'''-P(1),P(4)-四磷酸(Ap(4)A)储存在血小板致密颗粒中,但它对血小板功能的影响尚不清楚。

方法和结果

我们研究了 Ap(4)A 对血小板嘌呤能受体 P2Y(1)、P2Y(12)和 P2X(1)的影响。流式细胞术用于测量 Ap(4)A 在存在或不存在 ADP 的情况下对以下方面的影响:a)Ap(4)A 对 P2Y(12)介导的血小板内磷酸化血管扩张刺激磷蛋白(VASP)减少的影响,b)Ap(4)A 对 P2Y(1)介导的血小板胞质 Ca(2+)增加的影响,以及 c)Ap(4)A 对 P2X(1)介导的细胞外 Ca(2+)进入血小板的影响。ADP 刺激的血小板形态变化(P2Y(1)介导)和聚集(P2Y(1)和 P2Y(12)介导)通过光学方法进行测量。Ap(4)A 抑制 3μM ADP 诱导的:a)血小板聚集(IC(50)9.8+/-2.8μM),b)P2Y(1)介导的形态变化,c)P2Y(1)介导的血小板胞质 Ca(2+)增加(IC(50)40.8+/-12.3μM),以及 d)P2Y(12)介导的 VASP 磷酸化减少(IC(50)>250μM)。在没有添加 ADP 的情况下,Ap(4)A 对血小板 P2X(1)和 P2Y(12)受体具有激动剂作用,但对 P2Y(1)受体没有作用。

结论

Ap(4)A,血小板致密颗粒的组成部分,a)是血小板 P2Y(1)和 P2Y(12)受体的拮抗剂,在那里它抑制 ADP 的作用,以及 b)血小板 P2X(1)和 P2Y(12)受体的激动剂。

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