Papapetropoulos A, Piccardoni P, Cirino G, Bucci M, Sorrentino R, Cicala C, Johnson K, Zachariou V, Sessa W C, Altieri D C
Department of Pharmacology, Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, CT 06536, USA.
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4738-42. doi: 10.1073/pnas.95.8.4738.
The signaling pathway initiated by factor Xa on vascular endothelial cells was investigated. Factor Xa stimulated a 5- to 10-fold increased release of nitric oxide (NO) in a dose-dependent reaction (0.1-2.5 microG/ml) unaffected by the thrombin inhibitor hirudin but abolished by active site inhibitors, tick anticoagulant peptide, or Glu-Gly-Arg-chloromethyl ketone. In contrast, the homologous clotting protease factor IXa or another endothelial cell ligand, fibrinogen, was ineffective. A factor Xa inter-epidermal growth factor synthetic peptide L (83)FTRKL(88) (G) blocking ligand binding to effector cell protease receptor-1 inhibited NO release by factor Xa in a dose-dependent manner, whereas a control scrambled peptide KFTGRLL was ineffective. Catalytically active factor Xa induced hypotension in rats and vasorelaxation in the isolated rat mesentery, which was blocked by the NO synthase inhibitor L-N(G)-nitroarginine methyl ester (L-NAME) but not by D-NAME. Factor Xa/NO signaling also produced a dose-dependent endothelial cell release of interleukin 6 (range 0.55-3.1 ng/ml) in a reaction inhibited by L-NAME and by the inter-epidermal growth factor peptide Leu(83)-Leu(88) but unaffected by hirudin. Maximal induction of interleukin 6 mRNA required a brief, 30-min stimulation with factor Xa, unaffected by subsequent addition of tissue factor pathway inhibitor. These data suggest that factor Xa-induced NO release modulates endothelial cell-dependent vasorelaxation and cytokine gene expression. This pathway requiring factor Xa binding to effector cell protease receptor-1 and a secondary step of ligand-dependent proteolysis may preserve an anti-thrombotic phenotype of endothelium but also trigger acute phase responses during activation of coagulation in vivo.
研究了因子Xa在血管内皮细胞上启动的信号通路。因子Xa在剂量依赖性反应(0.1 - 2.5微克/毫升)中刺激一氧化氮(NO)释放增加5至10倍,该反应不受凝血酶抑制剂水蛭素的影响,但被活性位点抑制剂、蜱抗凝肽或Glu - Gly - Arg - 氯甲基酮所消除。相比之下,同源凝血蛋白酶因子IXa或另一种内皮细胞配体纤维蛋白原则无效。一种阻断配体与效应细胞蛋白酶受体-1结合的因子Xa表皮生长因子合成肽L(83)FTRKL(88)(G)以剂量依赖性方式抑制因子Xa诱导的NO释放,而对照乱序肽KFTGRLL则无效。具有催化活性的因子Xa可诱导大鼠低血压和离体大鼠肠系膜血管舒张,这被NO合酶抑制剂L - N(G)-硝基精氨酸甲酯(L - NAME)阻断,但不被D - NAME阻断。因子Xa/NO信号传导还在L - NAME和表皮生长因子肽Leu(83)-Leu(88)抑制的反应中产生剂量依赖性的内皮细胞白细胞介素6释放(范围为0.55 - 3.1纳克/毫升),但不受水蛭素影响。白细胞介素6 mRNA的最大诱导需要用因子Xa进行短暂的30分钟刺激,不受随后添加的组织因子途径抑制剂的影响。这些数据表明,因子Xa诱导的NO释放调节内皮细胞依赖性血管舒张和细胞因子基因表达。这条需要因子Xa与效应细胞蛋白酶受体-1结合以及配体依赖性蛋白水解第二步的信号通路可能维持内皮的抗血栓表型,但也可能在体内凝血激活过程中触发急性期反应。