Litvinov Rustem I, Weisel John W
Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
ISBT Sci Ser. 2017 Feb;12(1):176-183. doi: 10.1111/voxs.12331. Epub 2016 Dec 14.
In contrast to an obsolete notion that erythrocytes, or red blood cells (RBCs), play a passive and minor role in hemostasis and thrombosis, over the past decades there has been increasing evidence that RBCs have biologically and clinically important functions in blood clotting and its disorders. This review summarizes the main mechanisms that underlie the involvement of RBCs in hemostasis and thrombosis in vivo, such as rheological effects on blood viscosity and platelet margination, aggregation and deformability of RBCs; direct adhesion and indirect biochemical interactions with endothelial cells and platelets, etc. The ability of stored and pathologically altered RBCs to generate thrombin through exposure of phosphatidylserine has been emphasized. The procoagulant and prothrombotic potential of RBC-derived microparticles transfused with stored RBCs or formed in various pathological conditions associated with hemolysis has been described along with prothrombotic effects of free hemoglobin and heme. Binding of fibrinogen or fibrin to RBCs may influence their effects on fibrin network structure, clot mechanical properties, and fibrinolytic resistance. Recent data on platelet-driven clot contraction show that RBCs compressed by platelets pulling on fibrin form a tightly packed array of polyhedral erythrocytes, or polyhedrocytes, which comprises a nearly impermeable barrier important for hemostasis and wound healing. RBCs may perform dual roles, both helping to stem bleeding but at the same time contributing to thrombosis in a variety of ways.
与红细胞(或红血球,RBCs)在止血和血栓形成中起被动和次要作用这一过时观念相反,在过去几十年里,越来越多的证据表明红细胞在血液凝固及其紊乱过程中具有生物学和临床重要功能。本综述总结了红细胞在体内参与止血和血栓形成的主要机制,例如对血液粘度和血小板边缘化的流变学影响、红细胞的聚集和变形能力;与内皮细胞和血小板的直接粘附以及间接生化相互作用等。已强调储存和病理改变的红细胞通过暴露磷脂酰丝氨酸产生凝血酶的能力。描述了与储存红细胞一起输注或在与溶血相关的各种病理条件下形成的红细胞衍生微粒的促凝和促血栓形成潜力,以及游离血红蛋白和血红素的促血栓形成作用。纤维蛋白原或纤维蛋白与红细胞的结合可能会影响它们对纤维蛋白网络结构、凝块机械性能和纤维蛋白溶解抵抗的作用。关于血小板驱动的凝块收缩的最新数据表明,被血小板牵拉纤维蛋白而压缩的红细胞形成了紧密排列的多面体红细胞阵列,即多角红细胞,它构成了对止血和伤口愈合很重要的几乎不可渗透的屏障。红细胞可能发挥双重作用,既有助于止血,同时又以多种方式促成血栓形成。