Chen Buxin, Soto Antonio G, Coronel Luisa J, Goss Ashley, van Ryn Joanne, Trejo JoAnn
Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, California (B.C., A.G.C., L.J.C., J.T.); Department of CardioMetabolic Disease Research, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut (A.G.); and Department of CardioMetabolic Disease Research, Boehringer Ingelheim Pharma Gmbh, Biberach, Germany (J.R.).
Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, California (B.C., A.G.C., L.J.C., J.T.); Department of CardioMetabolic Disease Research, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut (A.G.); and Department of CardioMetabolic Disease Research, Boehringer Ingelheim Pharma Gmbh, Biberach, Germany (J.R.)
Mol Pharmacol. 2015 Jul;88(1):95-105. doi: 10.1124/mol.114.096446. Epub 2015 May 1.
Thrombin, the key effector protease of the coagulation cascade, drives fibrin deposition and activates human platelets through protease-activated receptor-1 (PAR1). These processes are critical to the progression of thrombotic diseases. Thrombin is the main target of anticoagulant therapy, and major efforts have led to the discovery of new oral direct inhibitors of thrombin. Dabigatran is the first oral anticoagulant licensed for the prevention of thromboembolisms associated with orthopedic surgery and stroke prevention in atrial fibrillation. Dabigatran is a direct thrombin inhibitor that effectively blocks thrombin's catalytic activity but does not preclude thrombin's exosites and binding to fibrinogen. Thus, we hypothesized that catalytically inactive thrombin retains the capacity to bind to PAR1 through exosite-I and may modulate its function independent of receptor cleavage and activation. Here, we report that dabigatran at clinically relevant concentrations is an effective and acute inhibitor of thrombin-induced PAR1 cleavage, activation, internalization, and β-arrestin recruitment in vitro. Interestingly, prolonged exposure to catalytic inactive thrombin incubated with dabigatran at 20-fold higher therapeutic concentration resulted in increased PAR1 cell-surface expression, which correlated with higher detectable levels of ubiquitinated receptor. These findings are consistent with ubiquitin function as a negative regulator of PAR1 constitutive internalization. Increased PAR1 expression also enhanced agonist-induced phosphoinositide hydrolysis and endothelial barrier permeability. Thus, catalytically inactive thrombin appears to modulate PAR1 function in vitro by stabilizing receptor cell-surface expression; but given the high clearance rate of thrombin, the high concentration of dabigatran required to achieve this effect the in vivo physiologic relevance is unknown.
凝血酶是凝血级联反应的关键效应蛋白酶,它通过蛋白酶激活受体-1(PAR1)驱动纤维蛋白沉积并激活人血小板。这些过程对于血栓性疾病的进展至关重要。凝血酶是抗凝治疗的主要靶点,人们付出了巨大努力,发现了新型口服直接凝血酶抑制剂。达比加群是首个获批用于预防骨科手术相关血栓栓塞和预防房颤中风的口服抗凝药。达比加群是一种直接凝血酶抑制剂,可有效阻断凝血酶的催化活性,但不排除凝血酶的外位点以及与纤维蛋白原的结合。因此,我们推测无催化活性的凝血酶保留了通过外位点-I与PAR1结合的能力,并且可能独立于受体裂解和激活来调节其功能。在此,我们报告在体外,临床相关浓度的达比加群是凝血酶诱导的PAR1裂解、激活、内化和β-抑制蛋白募集的有效急性抑制剂。有趣的是,在比治疗浓度高20倍的情况下,将无催化活性的凝血酶与达比加群长时间孵育,导致PAR1细胞表面表达增加,这与可检测到的泛素化受体水平升高相关。这些发现与泛素作为PAR1组成型内化的负调节因子的功能一致。PAR1表达增加还增强了激动剂诱导的磷酸肌醇水解和内皮屏障通透性。因此,无催化活性的凝血酶似乎通过稳定受体细胞表面表达在体外调节PAR1功能;但鉴于凝血酶的高清除率,在体内达到这种效果所需的高浓度达比加群的生理相关性尚不清楚。