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血小板释放产物可调节多形核白细胞激活的某些方面。

Platelet release products modulate some aspects of polymorphonuclear leukocyte activation.

作者信息

Allegrezza-Giulietti A, Serretti R, Beccerica E, Muti S, Ferretti G, Cervini C

机构信息

Institute of Rheumatology, Faculty of Medicine, University of Ancona, Italy.

出版信息

J Cell Biochem. 1991 Nov;47(3):242-50. doi: 10.1002/jcb.240470310.

DOI:10.1002/jcb.240470310
PMID:1838744
Abstract

The aim of this research was to evaluate in vitro interactions between platelets and polymorphonuclear leukocytes. The effects of supernatant from thrombin-activated platelets and two platelet release products (adenosine triphosphate and beta-thromboglobulin) were tested on the following features of polymorphonuclear leukocytes activation: opsonized zymosan and phorbol myristate acetate stimulated chemiluminescence, release of membrane bound calcium, NADPH-oxidase activity, and membrane fluidity (fluorescent polarization). The results showed that the addition of platelet supernatant to polymorphonuclear leukocytes induces a significant activation of cells. On the other hand, after three hours of preincubation of polymorphonuclear leukocytes with platelet supernatant, a decreased response of polymorphonuclear leukocytes to stimulation with phorbol myristate acetate, a significant decrease in NADPH-oxidase activity, and a lowered membrane fluidity were observed. Adenosine triphosphate modulated only opsonized zymosan stimulated chemiluminescence, with and without preincubation with polymorphonuclear leukocytes. Beta-thromboglobulin caused a decrease of the chemiluminescent response of polymorphonuclear leukocytes, using both agonists, with and without preincubation with polymorphonuclear leukocytes. Moreover beta-thromboglobulin only caused a decrease of the polymorphonuclear leukocytes membrane fluidity without preincubation with the cells. These results support the thesis that platelets have a "time-related" modulating activity on polymorphonuclear leukocytes.

摘要

本研究的目的是评估血小板与多形核白细胞之间的体外相互作用。测试了凝血酶激活血小板的上清液以及两种血小板释放产物(三磷酸腺苷和β-血小板球蛋白)对多形核白细胞激活的以下特征的影响:经调理的酵母聚糖和佛波酯肉豆蔻酸酯刺激的化学发光、膜结合钙的释放、NADPH氧化酶活性以及膜流动性(荧光偏振)。结果表明,向多形核白细胞中添加血小板上清液可诱导细胞的显著激活。另一方面,多形核白细胞与血小板上清液预孵育三小时后,观察到多形核白细胞对佛波酯肉豆蔻酸酯刺激的反应降低、NADPH氧化酶活性显著降低以及膜流动性降低。无论是否与多形核白细胞预孵育,三磷酸腺苷仅调节经调理的酵母聚糖刺激的化学发光。使用两种激动剂,无论是否与多形核白细胞预孵育,β-血小板球蛋白都会导致多形核白细胞化学发光反应降低。此外,β-血小板球蛋白仅在未与细胞预孵育的情况下导致多形核白细胞膜流动性降低。这些结果支持了血小板对多形核白细胞具有“时间相关”调节活性这一论点。

相似文献

1
Platelet release products modulate some aspects of polymorphonuclear leukocyte activation.血小板释放产物可调节多形核白细胞激活的某些方面。
J Cell Biochem. 1991 Nov;47(3):242-50. doi: 10.1002/jcb.240470310.
2
Beta-thromboglobulin and polymorphonuclear leukocytes activation. (Effects on chemiluminescence, release of membrane bound calcium, NADPH-oxidase activity and membrane fluidity).β-血小板球蛋白与多形核白细胞激活。(对化学发光、膜结合钙释放、NADPH氧化酶活性及膜流动性的影响)
Biochem Int. 1991 May;24(2):273-9.
3
Thrombin-activated human platelets release two NAP-2 variants that stimulate polymorphonuclear leukocytes.凝血酶激活的人血小板释放出两种刺激多形核白细胞的NAP-2变体。
Thromb Haemost. 1996 Nov;76(5):780-5.
4
Stimulated platelets release factor(s) affecting the in vitro response of human polymorphonuclear cells.受刺激的血小板释放影响人多形核细胞体外反应的因子。
J Leukoc Biol. 1990 Jul;48(1):7-14. doi: 10.1002/jlb.48.1.7.
5
Platelet enhancement of O2-. responses in stimulated human neutrophils. Identification of platelet factor as adenine nucleotide.血小板增强刺激的人中性粒细胞中O2-的反应。血小板因子鉴定为腺嘌呤核苷酸。
Lab Invest. 1988 Jan;58(1):37-47.
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Polymorphonuclear leukocyte membrane fluidity and cytosolic Ca(2+) content in young adults with acute myocardial infarction. Evaluation at the initial stage and after 12 months.急性心肌梗死青年患者的多形核白细胞膜流动性和胞浆钙离子含量。初始阶段及12个月后的评估。
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[Analysis of platelet-derived factors that modulate functions of polymorphonuclear leukocytes].[调节多形核白细胞功能的血小板衍生因子分析]
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[Increase in chemiluminescence induced by receptor-independent stimulation of polymorphonuclear cells from psoriatic patients].[银屑病患者多形核细胞非受体依赖性刺激诱导的化学发光增加]
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Inhibition of platelet function by polymorphonuclear leukocytes.多形核白细胞对血小板功能的抑制作用。
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Regulation of polymorphonuclear leukocyte function by platelets.血小板对多形核白细胞功能的调节。
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