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用于体外、血小板储存期间及心肺旁路手术中检测血小板活化的血小板膜标志物比较。

Comparison of platelet membrane markers for the detection of platelet activation in vitro and during platelet storage and cardiopulmonary bypass surgery.

作者信息

Metzelaar M J, Korteweg J, Sixma J J, Nieuwenhuis H K

机构信息

Department of Hematology, University Hospital Utrecht, The Netherlands.

出版信息

J Lab Clin Med. 1993 Apr;121(4):579-87.

PMID:8454940
Abstract

Changes in the platelet plasma membrane during activation were investigated by flow cytometry in a comparative study of in vitro platelet activation during platelet storage and cardiopulmonary bypass surgery. We studied changes in the expression of the plasma membrane glycoproteins lb and llla and CD31 antigen (PECAM-1), the alpha-granule membrane proteins GMP-140 (PADGEM, CD62 antigen) and GMP-33, and lysosomal integral membrane protein-CD63. A simultaneous change in the expression of the various glycoproteins induced by platelet activation was seen after thrombin stimulation in vitro and during platelet storage. Platelet activation in vivo in patients showed a more complex change in the expression of membrane glycoproteins. During cardiopulmonary bypass the mean fluorescence values for glycoprotein llla, GMP-33, and the percentage of GMP-140 and lysosome integral membrane protein-CD63 expressing platelets increased significantly. CD31 antigen expression was significantly decreased, whereas glycoprotein lb expression did not change. We conclude that flow cytometry is useful for the detection of changes in the expression of membrane glycoproteins induced by platelet activation in vitro and during platelet storage. Application of flow cytometry as clinical tool for screening platelet activation in patients or for identification of a prethrombotic state requires evaluation of a panel of platelet membrane glycoproteins because the changes in membrane expression may be different in various clinical situations.

摘要

在一项关于血小板储存和体外循环手术期间体外血小板激活的对比研究中,通过流式细胞术研究了激活过程中血小板质膜的变化。我们研究了质膜糖蛋白lb和llla以及CD31抗原(PECAM - 1)、α - 颗粒膜蛋白GMP - 140(PADGEM,CD62抗原)和GMP - 33以及溶酶体整合膜蛋白 - CD63的表达变化。在体外凝血酶刺激后以及血小板储存期间,可见血小板激活诱导的各种糖蛋白表达同时发生变化。患者体内的血小板激活显示膜糖蛋白表达发生了更复杂的变化。在体外循环期间,糖蛋白llla、GMP - 33的平均荧光值以及表达GMP - 140和溶酶体整合膜蛋白 - CD63的血小板百分比显著增加。CD31抗原表达显著降低,而糖蛋白lb表达未发生变化。我们得出结论,流式细胞术可用于检测体外及血小板储存期间血小板激活诱导的膜糖蛋白表达变化。将流式细胞术作为筛选患者血小板激活或识别血栓前状态的临床工具,需要评估一组血小板膜糖蛋白,因为在各种临床情况下膜表达的变化可能不同。

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