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Inhibitory effects of LDL-associated tissue factor pathway inhibitor

机译:LDL相关组织因子途径抑制剂的抑制作用

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Introduction Tissue factor pathway inhibitor (TFPI) is present in plasma as full-length free TFPI (TFPIα) and as C-terminally degraded forms mainly associated with low-density lipoprotein particles (LDL-TFPI). Addition of TFPIα to plasma induces a prolongation of the clotting time when tested in a diluted prothrombin time (dPT) assay, whereas no prolongation is observed with LDL-TFPI or truncated recombinant TFPI (TFPI1-161). The aim was to further characterize kinetic properties of purified LDL-TFPI in thrombin generation and chromogenic activity assays. Materials and Methods LDL-TFPI was purified from human plasma by sequential flotation ultracentrifugation. Thrombin generation was measured in human plasma or in FVIII-immunodepleted plasma using either 1 pM tissue factor and 4 μM phospholipids or 0.5 nM factor Xa (FXa) and 4 μM phospholipids, respectively. Results TFPIα prolonged the lag-phase and decreased the thrombin peak in tissue factor-induced thrombin generation, whereas LDL-TFPI exclusively decreased the peak height of thrombin without effecting the lag phase. Steady-state and transient kinetics showed that LDL-TFPI was a more potent inhibitor of FXa than TFPIα and TFPI 1-161, indicating that FXa inhibition was not rate determining for the lag phase, whereas it appeared to affect thrombin generation during the propagation phase. This was supported by FXa-induced thrombin generation showing that LDL-TFPI, compared with TFPIα, more actively decreased the peak height. Conclusions Our results suggest that LDL-TFPI affects thrombin generation during the propagation phase, and is kinetically different from TFPI1-161. It may therefore play a more prominent physiological role in vivo than hereto anticipated from dPT measurements.
机译:简介组织因子途径抑制剂(TFPI)在血浆中以全长游离TFPI(TFPIα)和C端降解形式存在,主要与低密度脂蛋白颗粒(LDL-TFPI)相关。在稀释的凝血酶原时间(dPT)分析中进行测试时,向血浆中添加TFPIα会导致凝血时间延长,而LDL-TFPI或截短的重组TFPI(TFPI1-161)则未观察到延长。目的是在凝血酶产生和生色活性测定中进一步表征纯化的LDL-TFPI的动力学特性。材料和方法通过连续浮选超速离心从人血浆中纯化LDL-TFPI。分别使用1 pM组织因子和4μM磷脂或0.5 nM因子Xa(FXa)和4μM磷脂在人血浆或FVIII免疫去除血浆中测量凝血酶的生成。结果TFPIα延长了组织因子诱导的凝血酶生成的滞后阶段并降低了凝血酶峰,而LDL-TFPI仅降低了凝血酶的峰高而没有影响滞后阶段。稳态和瞬态动力学表明,与TFPIα和TFPI 1-161相比,LDL-TFPI是更有效的FXa抑制剂,表明FXa抑制并不能决定滞后阶段,而似乎在繁殖阶段会影响凝血酶的产生。 。 FXa诱导的凝血酶生成支持了这一点,表明与TFPIα相比,LDL-TFPI更积极地降低了峰高。结论我们的结果表明LDL-TFPI在繁殖期会影响凝血酶的生成,并且在动力学上与TFPI1-161不同。因此,它在体内的生理作用可能比迄今为止从dPT测量中所预期的更为重要。

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