Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm S-171 76, Sweden.
Cell. 2009 Dec 11;139(6):1143-56. doi: 10.1016/j.cell.2009.11.001.
Platelets play a central role in thrombosis, hemostasis, and inflammation. We show that activated platelets release inorganic polyphosphate (polyP), a polymer of 60-100 phosphate residues that directly bound to and activated the plasma protease factor XII. PolyP-driven factor XII activation triggered release of the inflammatory mediator bradykinin by plasma kallikrein-mediated kininogen processing. PolyP increased vascular permeability and induced fluid extravasation in skin microvessels of mice. Mice deficient in factor XII or bradykinin receptors were resistant to polyP-induced leakage. PolyP initiated clotting of plasma via the contact pathway. Ablation of intrinsic coagulation pathway proteases factor XII and factor XI protected mice from polyP-triggered lethal pulmonary embolism. Targeting polyP with phosphatases interfered with procoagulant activity of activated platelets and blocked platelet-induced thrombosis in mice. Addition of polyP restored defective plasma clotting of Hermansky-Pudlak Syndrome patients, who lack platelet polyP. The data identify polyP as a new class of mediator having fundamental roles in platelet-driven proinflammatory and procoagulant disorders.
血小板在血栓形成、止血和炎症中起着核心作用。我们表明,活化的血小板释放无机多聚磷酸盐(polyP),这是一种由 60-100 个磷酸基团组成的聚合物,可直接结合并激活血浆蛋白酶因子 XII。多聚磷酸盐驱动的因子 XII 激活触发了由血浆激肽释放酶介导的激肽原加工释放炎症介质缓激肽。多聚磷酸盐增加了血管通透性,并诱导小鼠皮肤微血管中的液体渗出。缺乏因子 XII 或缓激肽受体的小鼠对多聚磷酸盐诱导的渗漏具有抗性。多聚磷酸盐通过接触途径引发血浆凝固。内在凝血途径蛋白酶因子 XII 和因子 XI 的缺失可保护小鼠免受多聚磷酸盐引发的致命性肺栓塞。用磷酸酶靶向 polyP 可干扰活化血小板的促凝活性,并阻止小鼠血小板诱导的血栓形成。添加 polyP 可恢复缺乏血小板 polyP 的 Hermansky-Pudlak 综合征患者的缺陷血浆凝血。这些数据表明 polyP 是一种新型介质,在血小板驱动的促炎和促凝障碍中具有重要作用。