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Comparison of the relative activities of inducing platelet apoptosis stimulated by various platelet-activating agents

机译:各种血小板活化剂刺激诱导血小板凋亡的相对活性比较

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Apoptosis-like events are known to occur in anuclear platelets. Although the mechanisms responsible for these events are still not completely understood, studies suggested that some platelet agonists can activate platelet apoptosis. However, the relative activities of various platelet agonists in inducing apoptosis have not yet been investigated. In the present study we explored this issue, and attempted to identify the correlation between platelet activation and apoptosis. In a platelet aggregation study, there were no significant differences respectively stimulated by arachidonic acid (AA; 100 M), ADP (20 μM), collagen (10 μg/mL), thrombin (0.1 U/mL), U46619 (10 μM), and A23187 (5 μM). In a subsequent study, we fixed these concentrations of agonists to further compare their relative activities in inducing platelet apoptosis. Our results found that thrombin, U46619, and A23187 possess stronger activities than the other agonists in inducing platelet apoptosis (i.e., phosphatidylserine exposure, mitochondrial membrane potential depolarization, eukaryotic initiation factor (eIF)2,and caspase activation). On the other hand, AA induced no apoptotic events in platelets. Based on this approach, we demonstrated for the first time that thrombin, U46619, and A23187, but not AA, possess stronger activity in inducing platelet apoptosis. In addition, we also found that platelet activation might not necessarily be associated with the occurrence of platelet apoptosis. The in vivo physiological function of the apoptotic machinery in platelets is not yet clearly understood, and needs to be further investigated in the future.
机译:已知凋亡样事件发生在无核血小板中。尽管导致这些事件的机制仍不完全清楚,但研究表明某些血小板激动剂可以激活血小板凋亡。然而,尚未研究各种血小板激动剂诱导细胞凋亡的相对活性。在本研究中,我们探讨了这个问题,并试图确定血小板活化与细胞凋亡之间的相关性。在血小板聚集研究中,花生四烯酸(AA; 100 M),ADP(20μM),胶原蛋白(10μg/ mL),凝血酶(0.1 U / mL),U46619(10μM)分别刺激没有显着差异。和A23187(5μM)。在随后的研究中,我们固定了这些浓度的激动剂,以进一步比较它们在诱导血小板凋亡中的相对活性。我们的研究结果发现,凝血酶,U46619和A23187在诱导血小板凋亡方面具有比其他激动剂更强的活性(即磷脂酰丝氨酸暴露,线粒体膜电位去极化,真核启动因子(eIF)2和胱天蛋白酶激活)。另一方面,AA不会诱导血小板凋亡。基于这种方法,我们首次证明了凝血酶,U46619和A23187(而不是AA)在诱导血小板凋亡方面具有更强的活性。此外,我们还发现血小板活化不一定与血小板凋亡的发生有关。血小板中凋亡机制的体内生理功能尚不清楚,因此需要在未来进行进一步研究。

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