Riewald Matthias, Ruf Wolfram
Department of Immunology C204, The Scripps Research Institute, La Jolla, CA 92037, USA.
Trends Cardiovasc Med. 2002 May;12(4):149-54. doi: 10.1016/s1050-1738(02)00153-6.
Protease-activated receptors (PARs) are vascular sensors for signaling of the trypsinlike coagulation serine proteases that play key roles in cardiovascular medicine. In the initiation phase of coagulation, tissue factor (TF) orchestrates the assembly of VIIa with substrate X, forming a ternary complex in which product Xa is generated. The resulting TF-VIIa-Xa complex is an efficient activator of PAR1 and PAR2. TF initiation of the coagulation cascade is thus intimately linked to inflammatory cell signaling. Inflammation is an increasingly appreciated component of the vulnerable atherosclerotic plaque. Targeting inflammatory cell signaling events of the coagulation system may become an important aspect of efforts to improve antithrombotic therapy.
蛋白酶激活受体(PARs)是血管传感器,用于类胰蛋白酶凝血丝氨酸蛋白酶的信号传导,这些蛋白酶在心血管医学中发挥关键作用。在凝血起始阶段,组织因子(TF)协调VIIa与底物X的组装,形成一种三元复合物,其中产生产物Xa。由此产生的TF-VIIa-Xa复合物是PAR1和PAR2的有效激活剂。因此,凝血级联反应的TF起始与炎症细胞信号传导密切相关。炎症是易损动脉粥样硬化斑块中越来越受重视的一个组成部分。针对凝血系统的炎症细胞信号传导事件可能成为改善抗血栓治疗努力的一个重要方面。