血小板微粒促进血小板与子内皮质基质的相互作用,在依赖于糖蛋白IIb/IIIa的机制中
M Merten1, R Pakala, P Thiagarajan
1Department of Internal Medicine, Division of Hematology, University of Texas Houston Medical School, Houston, 77030, USA.
Circulation
|May 20, 1999
概括
血小板微粒与血管壁结合在一起.
科学领域:
- 血液学 血液学 血液学
- 血管生物学 血管生物学
- 生物化学 生物化学
背景情况:
- 血小板在激活时释放微粒.
- 这些微粒在血小板血管壁相互作用中的作用仍然不清楚.
研究的目的:
- 为了研究血小板微粒与血管壁部件的结合.
- 阐明这种相互作用的机制和功能意义.
主要方法:
- 用涂层表面和内皮细胞进行体外结合试验.
- 在动脉损伤的子模型的体内研究.
- 用GP IIb/IIIa抑制剂和单克隆抗体进行抑制研究.
主要成果:
- 血小板微粒与纤维素素,纤维菌素和原结合.
- 对细胞外基质的结合在体外观察到,并在体内受伤部位增强.
- GP IIb/IIIa抑制剂部分阻断了与矩阵组件的结合.
- 活化血小板以GP IIb/IIIa-依赖的方式粘附于微粒.
结论:
- 血小板微粒粘附在子内皮质基质上.
- 它们在受伤部位作为后续血小板聚合的平台.
- 这种相互作用对于血管损伤中血小板粘附至关重要.
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