Poole A W, Heath M F, Evans R J
University of Cambridge, Department of Clinical Veterinary Medicine.
Res Vet Sci. 1993 Mar;54(2):235-43. doi: 10.1016/0034-5288(93)90063-l.
Pre-incubation of equine platelets in platelet-rich plasma with adenosine 5'-diphosphate (ADP) induced a reduction in aggregation responsiveness to subsequent additions of ADP. The desensitisation was shown to be homologous since the responsiveness to platelet-activating factor, thrombin, collagen, 5-hydroxytryptamine or ionomycin remained unchanged. Adenosine 5'-(beta-thio)-diphosphate (ADP beta S), a non-hydrolysable analogue of ADP, was shown to act as an agonist inducing aggregation by interaction with the ADP receptor. ADP beta S was then used in the desensitisation studies in which residual ADP was degraded by the addition of apyrase. The desensitisation to ADP beta S fully recovered by one hour after pre-treatment with ADP and was not induced by an extracellular mediator. The mechanism of desensitisation is therefore likely to involve the ADP receptor or proximal intermediates in the signal transduction pathway for ADP.
用5'-二磷酸腺苷(ADP)对富含血小板血浆中的马血小板进行预孵育,会导致其对随后添加的ADP的聚集反应性降低。脱敏作用表现为同源性,因为对血小板活化因子、凝血酶、胶原蛋白、5-羟色胺或离子霉素的反应性保持不变。5'-(β-硫代)二磷酸腺苷(ADPβS)是一种ADP的不可水解类似物,已证明它可作为激动剂,通过与ADP受体相互作用诱导聚集。然后将ADPβS用于脱敏研究,其中通过添加腺苷三磷酸双磷酸酶降解残留的ADP。在用ADP预处理1小时后,对ADPβS的脱敏作用完全恢复,且不是由细胞外介质诱导的。因此,脱敏机制可能涉及ADP受体或ADP信号转导途径中的近端中间体。