Yao Yanling, Chen Yanqiu, Adili Reheman, McKeown Thomas, Chen Pingguo, Zhu Guangheng, Li Dan, Ling Wenhua, Ni Heyu, Yang Yan
Department of Nutrition, School of Public Health, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, People's Republic of China.
J Nutr. 2017 Oct;147(10):1917-1925. doi: 10.3945/jn.116.245944. Epub 2017 Aug 30.
Platelets play an important role in hemostasis, thrombosis, and atherosclerosis. Glycoprotein VI (GPVI) is a major platelet receptor that interacts with exposed collagen on injured vessel walls. Our previous studies have shown that anthocyanins (a type of natural plant pigment) attenuate platelet function; however, whether anthocyanins affect collagen-induced GPVI signaling remains unknown. The objective of this study was to explore the effects of cyanidin-3-glucoside (Cy-3-g, one of the major bioactive compounds in anthocyanins) on platelet activation and thrombosis and the GPVI signaling pathway. Platelets from healthy men and women were isolated and incubated with different concentrations (0, 0.5, 5, and 50 μM) of Cy-3-g. The expression of activated integrin αIIbβ3, P-selectin, CD63, and CD40L, fibrinogen binding to platelets, and platelet aggregation were evaluated in vitro. Platelet adhesion and aggregation in whole blood under flow conditions were assessed in collagen-coated perfusion chambers. Thrombosis and hemostasis were assessed in 3-4-wk-old male C57BL/6J mice through FeCl-induced intravital microscopy and tail bleeding time. The effect of Cy-3-g on collagen-induced human platelet GPVI signaling was explored with Western blot. Cy-3-g attenuated platelet function in a dose-dependent manner. The 0.5-μM dose of Cy-3-g inhibited ( < 0.05) human platelet adhesion and aggregation to collagen at both venous (-54.02%) and arterial (-22.90%) shear stresses. The 5-μM dose inhibited ( < 0.05) collagen-induced human platelet activation (PAC-1: -48.21%, P-selectin: -50.63%), secretion (CD63: -73.89%, CD40L: -43.70%), fibrinogen binding (-56.79%), and aggregation (-17.81%). The 5-μM dose attenuated ( < 0.01) thrombus growth (-66.67%) without prolonging bleeding time in mice. The 50-μM dose downregulated ( < 0.05) collagen-induced GPVI signaling in human platelets and significantly decreased phosphorylation of Syk-linker for activation of T cells (LAT)-SLP76 (Syk: -39.08%, LAT: -32.25%, SLP76: -40.00%) and the expression of Lyn (-31.89%), Fyn (-36.27%), and phospholipase C-γ2 (-39.08%). Cy-3-g inhibits human platelet activation, aggregation, secretion, and thrombus formation, and downregulates the collagen-GPVI signaling pathway. Supplementation of Cy-3-g may have protective effects against atherothrombosis.
血小板在止血、血栓形成和动脉粥样硬化过程中发挥着重要作用。糖蛋白VI(GPVI)是一种主要的血小板受体,可与受损血管壁上暴露的胶原蛋白相互作用。我们之前的研究表明,花青素(一种天然植物色素)可减弱血小板功能;然而,花青素是否影响胶原蛋白诱导的GPVI信号传导仍不清楚。本研究的目的是探讨花青素的主要生物活性成分之一矢车菊素 - 3 - 葡萄糖苷(Cy - 3 - g)对血小板活化、血栓形成及GPVI信号通路的影响。分离健康男性和女性的血小板,并与不同浓度(0、0.5、5和50 μM)的Cy - 3 - g孵育。体外评估活化的整合素αIIbβ3、P - 选择素、CD63和CD40L的表达、纤维蛋白原与血小板的结合以及血小板聚集情况。在胶原蛋白包被的灌注室中评估流动条件下全血中的血小板黏附和聚集。通过FeCl诱导的活体显微镜检查和尾部出血时间评估3 - 4周龄雄性C57BL / 6J小鼠的血栓形成和止血情况。采用蛋白质免疫印迹法探讨Cy - 3 - g对胶原蛋白诱导的人血小板GPVI信号传导的影响。Cy - 3 - g以剂量依赖的方式减弱血小板功能。0.5 μM剂量的Cy - 3 - g在静脉(-54.02%)和动脉(-22.90%)剪切应力下均抑制(P < 0.05)人血小板与胶原蛋白的黏附和聚集。5 μM剂量抑制(P < 0.05)胶原蛋白诱导的人血小板活化(PAC - 1:-48.21%,P - 选择素:-50.63%)、分泌(CD63:-73.89%,CD40L:-43.70%)、纤维蛋白原结合(-56.79%)和聚集(-17.81%)。5 μM剂量减弱(P < 0.01)小鼠血栓生长(-66.67%),且不延长出血时间。50 μM剂量下调(P < 0.05)胶原蛋白诱导的人血小板GPVI信号传导,并显著降低Syk - 衔接蛋白T细胞活化连接蛋白(LAT) - SLP76的磷酸化(Syk:-3Syk:-39.08%,LAT:-32.25%,SLP76:-40.00%)以及Lyn(-31.89%)、Fyn(-36.27%)和磷脂酶C - γ2(-39.08%)的表达。Cy - 3 - g抑制人血小板活化、聚集、分泌和血栓形成,并下调胶原蛋白 - GPVI信号通路。补充Cy - 3 - g可能对动脉粥样硬化血栓形成具有保护作用。