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用ADP在正常血浆中激活的血小板上纤维蛋白原受体表达的异质性:流式细胞术分析

Heterogeneity of fibrinogen receptor expression on platelets activated in normal plasma with ADP: analysis by flow cytometry.

作者信息

Jackson C W, Jennings L K

机构信息

Division of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38105.

出版信息

Br J Haematol. 1989 Jul;72(3):407-14. doi: 10.1111/j.1365-2141.1989.tb07724.x.

Abstract

Fibrinogen receptor expression of platelets activated in normal plasma by ADP was measured by flow cytometry after labelling bound fibrinogen with fluorescein-conjugated antifibrinogen antibody. The platelet response to ADP was heterogeneous both with respect to number of platelets binding fibrinogen and the amount of fibrinogen bound per platelet. The proportion of platelets showing positive antifibrinogen antibody binding increased with increasing ADP concentration; however, even at 10(-3) M ADP, usually about one-fifth of the platelets failed to demonstrate bound fibrinogen. The non-responsive platelets tended to be the smaller ones. The relative fluorescence intensity of individual platelets also increased as ADP concentration was increased, indicating that the average number of fibrinogen molecules bound was also related to agonist concentration. The amount of fibrinogen bound following platelet activation directly correlated with the quantity of surface glycoprotein IIb detected by Tab antibody and with platelet size. This study demonstrates that platelet response to ADP in native plasma is heterogeneous in both the proportion of platelets activated and in the number of available fibrinogen receptors per platelet. This heterogeneity is related to platelet size and glycoprotein IIb-IIIa content. These observations indicate that models of ligand interaction with membrane receptors on intact cells requiring an exposure step must take into account the heterogeneity of response within a cell population. In addition to providing new insights into the response of individual platelets to activation, these results suggest that study of platelet bound fibrinogen by flow cytometry may be useful for the detection of platelet activation in vivo.

摘要

用异硫氰酸荧光素标记的抗纤维蛋白原抗体标记结合的纤维蛋白原后,通过流式细胞术检测正常血浆中由ADP激活的血小板的纤维蛋白原受体表达。血小板对ADP的反应在结合纤维蛋白原的血小板数量和每个血小板结合的纤维蛋白原量方面都是异质性的。显示抗纤维蛋白原抗体结合阳性的血小板比例随ADP浓度增加而增加;然而,即使在10⁻³M ADP时,通常仍约有五分之一的血小板未能显示结合纤维蛋白原。无反应的血小板往往较小。随着ADP浓度增加,单个血小板的相对荧光强度也增加,表明结合的纤维蛋白原分子平均数量也与激动剂浓度有关。血小板激活后结合的纤维蛋白原量与Tab抗体检测到的表面糖蛋白IIb量以及血小板大小直接相关。本研究表明,天然血浆中血小板对ADP的反应在激活的血小板比例和每个血小板可用的纤维蛋白原受体数量方面都是异质性的。这种异质性与血小板大小和糖蛋白IIb-IIIa含量有关。这些观察结果表明,需要暴露步骤的完整细胞上配体与膜受体相互作用的模型必须考虑细胞群体内反应的异质性。除了为单个血小板对激活的反应提供新的见解外,这些结果还表明,通过流式细胞术研究血小板结合的纤维蛋白原可能有助于体内血小板激活的检测。

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