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Several platelet receptors and their ligands are involved in platelet- dependent thrombus formation

机译:几种血小板受体及其配体参与血小板依赖性血栓的形成

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摘要

I thank Drs. Kounis and Grapsas [1] for having read and commented my editorial [2] on the study by Shi et al, which showed that decreased platelet miR-223 expression is associated with high responsiveness to adenosine diphosphate (ADP) [3]. The findings by Shi et al are consistent with the demonstration that miR-223 regulates the expression of the platelet receptor for ADP, P2Y12 [4]. Because the patient population that was studied by Shi et al was on treatment with clopidogrel, which inhibits the platelet ADP receptor P2Y12, the authors concluded that decreased platelet miR-223 expression is associated with high on treatment platelet reactivity (HTPR) on clopidogrel, which was measured using 2 methods: the VASP phosphorylation assay and ADP-induced platelet aggregation (light transmission aggregometry). Therefore, if the results by Shi and collaborators will be confirmed by larger studies, low miR-223 expression could add to the long list of conditions that are associated with HTPR on clopidogrel [5,6].
机译:我感谢博士。 Kounis和Grapsas [1]阅读并评论了Shi等人的研究的评论[2],该研究表明血小板miR-223表达降低与对二磷酸腺苷(ADP)的高响应性相关[3]。 Shi等人的发现与miR-223调节ADP P2Y12血小板受体表达的研究一致[4]。由于Shi等人研究的患者群体正在接受氯吡格雷治疗,从而抑制了血小板ADP受体P2Y12,因此作者得出结论,降低血小板miR-223的表达与氯吡格雷对血小板的高治疗反应性(HTPR)有关,使用两种方法进行测量:VASP磷酸化分析和ADP诱导的血小板聚集(光凝集法)。因此,如果Shi和合作者的结果将被更大的研究证实,那么miR-223的低表达可能会增加氯吡格雷与HTPR相关的条件[5,6]。

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