Peerschke E I
J Lab Clin Med. 1985 Aug;106(2):111-22.
The mechanism of adenosine diphosphate (ADP)-induced refractoriness was explored with iodine 125-labeled fibrinogen and the fluorescent Ca+2 indicator quin-2-tetraacetoxymethyl ester (quin-2). Gel-filtered platelets were rendered refractory by incubation (30 minutes, 22 degrees C) with either 10 mumol/L ADP alone or ADP and 125I-labeled fibrinogen. During the incubation period, platelets incubated with ADP alone showed an initial increase in quin-2 fluorescence, which gradually returned to baseline levels. Addition of 125I-fibrinogen to aliquots of the platelet suspension at various times during incubation showed that fibrinogen binding was normal after 1 minute but decreased to 50% in 30 minutes. According to Scatchard analysis, this decreased binding was attributed to decreased fibrinogen receptor availability, not decreased receptor affinity. Moreover, similar numbers of glycoprotein (GP) IIb-IIIa complexes remained available on platelets before and after incubation, as judged by the ability of a monoclonal antibody (10E5) directed against a complex specific epitope on GPIIb or IIIa to bind to control and refractory platelets. After incubation, platelets aggregated poorly in response to restimulation with ADP, although the amount of fibrinogen they bound (50% of normal) was sufficient to aggregate control platelets. Platelet restimulation with ADP was not accompanied by a rise in quin-2 fluorescence or exposure of additional fibrinogen receptors. Stimulation of platelets with thrombin, however, led to a rise in quin-2 fluorescence, exposure of additional fibrinogen receptors, and enhanced aggregation. Restimulation of platelets with epinephrine also increased fibrinogen receptor exposure and restored the ability of platelets to aggregate, but was accompanied by barely detectable changes in quin-2 fluorescence similar to those observed with epinephrine-treated control platelets. Platelets incubated for 30 minutes with ADP and 125I-fibrinogen also showed an initial rise in quin-2 fluorescence, which returned to baseline levels during incubation, but the amount of platelet-bound fibrinogen, normal at the onset, remained quantitatively unchanged. Much of this fibrinogen, however, no longer dissociated from platelets in the presence of ethylenediaminetetraacetic acid or apyrase, suggesting that a different type of platelet-fibrinogen interaction had developed. Restimulation of these platelets with ADP was not accompanied by increased fibrinogen binding or quin-2 fluorescence and failed to elicit significant platelet aggregation.(ABSTRACT TRUNCATED AT 400 WORDS)
采用碘125标记的纤维蛋白原和荧光钙指示剂喹啉-2-四乙酰氧基甲酯(quin-2),对二磷酸腺苷(ADP)诱导的不应性机制进行了研究。通过单独用10 μmol/L ADP或ADP与125I标记的纤维蛋白原孵育(30分钟,22℃),使凝胶过滤的血小板产生不应性。在孵育期间,单独用ADP孵育的血小板显示quin-2荧光最初增加,随后逐渐恢复到基线水平。在孵育期间的不同时间,向血小板悬液的等分试样中加入125I-纤维蛋白原,结果显示1分钟后纤维蛋白原结合正常,但30分钟后降至50%。根据Scatchard分析,这种结合减少归因于纤维蛋白原受体可用性降低,而非受体亲和力降低。此外,通过针对GPIIb或IIIa上复合特异性表位的单克隆抗体(10E5)与对照血小板和不应性血小板结合的能力判断,孵育前后血小板上可用的糖蛋白(GP)IIb-IIIa复合物数量相似。孵育后,尽管血小板结合的纤维蛋白原量(正常量的50%)足以使对照血小板聚集,但用ADP再次刺激时血小板聚集不良。用ADP再次刺激血小板并未伴随quin-2荧光升高或额外纤维蛋白原受体的暴露。然而,用凝血酶刺激血小板会导致quin-2荧光升高、额外纤维蛋白原受体暴露以及聚集增强。用肾上腺素再次刺激血小板也会增加纤维蛋白原受体暴露并恢复血小板聚集能力,但伴随的quin-2荧光变化几乎难以检测到,类似于用肾上腺素处理的对照血小板所观察到的变化。用ADP和125I-纤维蛋白原孵育30分钟的血小板也显示quin-2荧光最初升高,在孵育期间恢复到基线水平,但开始时正常的血小板结合纤维蛋白原量在数量上保持不变。然而,在存在乙二胺四乙酸或腺苷三磷酸双磷酸酶的情况下,这些纤维蛋白原中的许多不再从血小板上解离,这表明已形成了一种不同类型的血小板-纤维蛋白原相互作用。用ADP再次刺激这些血小板并未伴随纤维蛋白原结合增加或quin-2荧光升高,也未能引发显著的血小板聚集。(摘要截短至400字)