Millington-Burgess Sarah Louise, Bonna Arkadiusz M, Rahman Taufiq, Harper Matthew Thomas
Department of Pharmacology, University of Cambridge, Cambridge, UK.
CambCol Laboratories, Ely, Cambridgeshire, UK.
Br J Pharmacol. 2020 Sep;177(17):4007-4020. doi: 10.1111/bph.15152. Epub 2020 Jun 30.
Ethaninidothioic acid (R5421) has been used as a scramblase inhibitor to determine the role of phospholipid scrambling across a range of systems including platelet procoagulant activity. The selectivity of R5421 has not been thoroughly studied. Here, we characterised the effects of R5421 on platelet function and its suitability for use as a scramblase inhibitor.
Human platelet activation was measured following pretreatment with R5421 and stimulation with a range of agonists. Phosphatidylserine exposure was measured using annexin V binding. Integrin α β activation and α-granule release were measured by flow cytometry. Cytosolic Ca signals were measured using Cal520 fluorescence. An in silico ligand-based screen identified 16 compounds which were tested in these assays.
R5421 inhibited A23187-induced phosphatidylserine exposure in a time- and temperature-dependent manner. R5421 inhibited Ca signalling from the PAR1, PAR4 and glycoprotein VI receptors as well as platelet α β integrin activation and α-granule release. R5421 is therefore not a selective inhibitor of platelet scramblase activity. An in silico screen identified the pesticide thiodicarb as similar to R5421. It also inhibited platelet phosphatidylserine exposure, Ca signalling from the PAR1 and glycoprotein VI, α β activation and α-granule release. Thiodicarb additionally disrupted Ca homeostasis in unstimulated platelets.
R5421 is not a selective inhibitor of platelet scramblase activity. We have identified the pesticide thiodicarb, which had similar effects on platelet function to R5421 as well as additional disruption of Ca signalling which may underlie some of thiodicarb's toxicity.
乙硫代酸(R5421)已被用作一种翻转酶抑制剂,以确定磷脂翻转在包括血小板促凝活性在内的一系列系统中的作用。R5421的选择性尚未得到充分研究。在此,我们表征了R5421对血小板功能的影响及其作为翻转酶抑制剂的适用性。
用R5421预处理后,再用一系列激动剂刺激,测量人血小板活化情况。使用膜联蛋白V结合来测量磷脂酰丝氨酸暴露。通过流式细胞术测量整合素αβ活化和α颗粒释放。使用Cal520荧光测量胞质钙信号。基于计算机配体的筛选鉴定出16种化合物,并在这些实验中进行了测试。
R5421以时间和温度依赖性方式抑制A23187诱导的磷脂酰丝氨酸暴露。R5421抑制来自PAR1、PAR4和糖蛋白VI受体的钙信号传导以及血小板αβ整合素活化和α颗粒释放。因此,R5421不是血小板翻转酶活性的选择性抑制剂。基于计算机的筛选鉴定出农药硫双威与R5421相似。它还抑制血小板磷脂酰丝氨酸暴露、来自PAR1和糖蛋白VI的钙信号传导、αβ活化和α颗粒释放。硫双威还破坏了未刺激血小板中的钙稳态。
R5421不是血小板翻转酶活性的选择性抑制剂。我们鉴定出了农药硫双威,其对血小板功能的影响与R5421相似,并且还额外破坏了钙信号传导,这可能是硫双威某些毒性的基础。