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凝血酶诱导的血小板分泌。特定途径的进一步证据。

Thrombin-induced platelet secretion. Further evidence for a specific pathway.

作者信息

Shuman M A, Botney M, Fenton J W

出版信息

J Clin Invest. 1979 Jun;63(6):1211-8. doi: 10.1172/JCI109416.

Abstract

We have studied the interaction between thrombin and washed, human platelets using prostacyclin, a reversible inhibitor of platelet secretion. The effect of thrombin is limited to those reactions that are not inhibited by an increased concentration of platelet cyclic adenosine 3',5'-monophosphate, because prostacyclin is a potent inducer of the latter. Prostacyclin-treated platelets were briefly (15-30 s) exposed to low concentrations of human thrombin (0.01-0.2 U/ml). After removal of the prostacyclin and thrombin, the platelets were incubated with fresh thrombin. Although they had not undergone the release reaction after the first thrombin incubation, these platelets had a diminished capacity to secrete [(3)H]serotonin when exposed to thrombin the second time. Refractoriness was concentration dependent: the higher the initial thrombin concentration, the greater the degree of inhibition of serotonin secretion on subsequent thrombin exposure. Inhibition was closely related to the ability of thrombin to induce platelet secretion and not to its esterase or fibrinogen clotting activity. Diisopropyl fluorophosphate-inactive thrombin did not induce refractoriness. Refractoriness to thrombin did not increase when the time of the initial incubation with thrombin was lengthened, nor was it reversible.INHIBITION WAS THROMBIN SPECIFIC: serotonin secretion induced by collagen, wheat germ agglutinin, and the ionophore A23187 was minimally affected. For an equivalent amount of thrombin bound, a decrease was observed in serotonin secretion by thrombin-pretreated platelets compared to control platelets. Thus, there is at least one step in the secretory pathway between thrombin binding and regulation of adenylate cyclase. This step appears to transmit the signal that leads to extrusion of intracellular granular contents.

摘要

我们使用前列环素(一种血小板分泌的可逆抑制剂)研究了凝血酶与洗涤后的人血小板之间的相互作用。凝血酶的作用仅限于那些不受血小板环磷酸腺苷(cAMP)浓度升高抑制的反应,因为前列环素是后者的强效诱导剂。用前列环素处理过的血小板短暂(15 - 30秒)暴露于低浓度的人凝血酶(0.01 - 0.2 U/ml)。去除前列环素和凝血酶后,将血小板与新鲜凝血酶一起孵育。尽管这些血小板在第一次凝血酶孵育后未发生释放反应,但当再次暴露于凝血酶时,它们分泌[³H]5-羟色胺的能力有所下降。不应性呈浓度依赖性:初始凝血酶浓度越高,随后再次暴露于凝血酶时5-羟色胺分泌的抑制程度就越大。抑制作用与凝血酶诱导血小板分泌的能力密切相关,而与其酯酶或纤维蛋白原凝血活性无关。二异丙基氟磷酸失活的凝血酶不会诱导不应性。当延长与凝血酶的初始孵育时间时,对凝血酶的不应性不会增加,也不可逆转。抑制作用具有凝血酶特异性:胶原、麦胚凝集素和离子载体A23187诱导的5-羟色胺分泌受到的影响最小。对于等量结合的凝血酶,与对照血小板相比,凝血酶预处理的血小板中5-羟色胺分泌减少。因此,在凝血酶结合与腺苷酸环化酶调节之间的分泌途径中至少存在一个步骤。这个步骤似乎传递了导致细胞内颗粒内容物挤出的信号。

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