Martínez-Sales V, Vila V, Réganon E, Aznar J
Research Center, University Hospital La Fe, Valencia, Spain.
Haemostasis. 1995 Jul-Aug;25(4):158-65. doi: 10.1159/000217156.
The binding of unstimulated and thrombin-stimulated platelets was studied with immobilized fibrinogen and fibrin on polystyrene. The amount of fibrinogen bound to the polystyrene support was 2 micrograms/tube, which represents 2.35 micrograms/cm2. Immobilized fibrin was obtained by adding thrombin (5 nM) to immobilized fibrinogen. The number of unstimulated 111In-platelets bound to immobilized fibrinogen and fibrin was similar (3.2 +/- 0.3 x 10(6) and 3.1 +/- 0.4 x 10(6) platelets/micrograms fibrin(ogen), respectively). The platelet binding steadily increased. In the first 2 min, the binding rate was 0.23 x 10(6) platelets/micrograms fibrinogen/min. The binding rate then increased rapidly and saturation was reached at 10 min. The extent of the adhesion of resting platelets to immobilized fibrinogen is about one half that of the same platelets stimulated with thrombin. In thrombin-stimulated 111In-platelets, the binding to immobilized fibrinogen and fibrin is time dependent, and saturation is reached at 5 min. The early rate of thrombin-stimulated platelet binding to fibrinogen is about twice that of binding to fibrin (1.25 and 0.74 x 10(6) platelets/micrograms fibrin(ogen)/min, respectively). In saturation conditions, 1 microgram fibrinogen binds 5.7 +/- 0.6 x 10(6) thrombin-stimulated platelets and 1 microgram fibrin binds 4.6 +/- 0.5 x 10(6) thrombin-stimulated platelets. Our results indicate that the rate of platelet aggregation is faster than fibrin formation, and the rate of fibrinogen-platelet binding is faster than that of fibrin-platelet binding. Therefore, after thrombin stimulation, the binding of platelets to fibrin must be secondary to the binding of platelets to fibrinogen.
利用固定在聚苯乙烯上的纤维蛋白原和纤维蛋白,研究了未受刺激和凝血酶刺激的血小板的结合情况。结合到聚苯乙烯载体上的纤维蛋白原量为2微克/管,相当于2.35微克/平方厘米。通过向固定的纤维蛋白原中加入凝血酶(5纳摩尔)获得固定的纤维蛋白。与固定的纤维蛋白原和纤维蛋白结合的未受刺激的铟 - 111标记血小板数量相似(分别为3.2±0.3×10⁶和3.1±0.4×10⁶血小板/微克纤维蛋白(原))。血小板结合稳步增加。在最初2分钟内,结合速率为0.23×10⁶血小板/微克纤维蛋白原/分钟。然后结合速率迅速增加,并在10分钟时达到饱和。静息血小板与固定纤维蛋白原的黏附程度约为相同血小板经凝血酶刺激后黏附程度的一半。在凝血酶刺激的铟 - 111标记血小板中,与固定纤维蛋白原和纤维蛋白的结合是时间依赖性的,并在5分钟时达到饱和。凝血酶刺激的血小板与纤维蛋白原结合的早期速率约为与纤维蛋白结合速率的两倍(分别为1.25和0.74×10⁶血小板/微克纤维蛋白(原)/分钟)。在饱和条件下,1微克纤维蛋白原结合5.7±0.6×10⁶凝血酶刺激的血小板,1微克纤维蛋白结合4.6±0.5×10⁶凝血酶刺激的血小板。我们的结果表明,血小板聚集速率比纤维蛋白形成速率快,纤维蛋白原 - 血小板结合速率比纤维蛋白 - 血小板结合速率快。因此,凝血酶刺激后,血小板与纤维蛋白的结合必定继发于血小板与纤维蛋白原的结合。