Vatsyayan Rit, Kothari Hema, Mackman Nigel, Pendurthi Usha R, Rao L Vijaya Mohan
Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, Texas, United States of America.
Division of Hematology and Oncology, McAllister Heart Institute, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
PLoS One. 2014 Aug 7;9(8):e103505. doi: 10.1371/journal.pone.0103505. eCollection 2014.
Recent studies have suggested that antithrombin (AT) could act as a significant physiologic regulator of FVIIa. However, in vitro studies showed that AT could inhibit FVIIa effectively only when it was bound to tissue factor (TF). Circulating blood is known to contain only traces of TF, at best. FVIIa also binds endothelial cell protein C receptor (EPCR), but the role of EPCR on FVIIa inactivation by AT is unknown. The present study was designed to investigate the role of TF and EPCR in inactivation of FVIIa by AT in vivo. Low human TF mice (low TF, ∼ 1% expression of the mouse TF level) and high human TF mice (HTF, ∼ 100% of the mouse TF level) were injected with human rFVIIa (120 µg kg(-1) body weight) via the tail vein. At varying time intervals following rFVIIa administration, blood was collected to measure FVIIa-AT complex and rFVIIa antigen levels in the plasma. Despite the large difference in TF expression in the mice, HTF mice generated only 40-50% more of FVIIa-AT complex as compared to low TF mice. Increasing the concentration of TF in vivo in HTF mice by LPS injection increased the levels of FVIIa-AT complexes by about 25%. No significant differences were found in FVIIa-AT levels among wild-type, EPCR-deficient, and EPCR-overexpressing mice. The levels of FVIIa-AT complex formed in vitro and ex vivo were much lower than that was found in vivo. In summary, our results suggest that traces of TF that may be present in circulating blood or extravascular TF that is transiently exposed during normal vessel damage contributes to inactivation of FVIIa by AT in circulation. However, TF's role in AT inactivation of FVIIa appears to be minor and other factor(s) present in plasma, on blood cells or vascular endothelium may play a predominant role in this process.
最近的研究表明,抗凝血酶(AT)可能是FVIIa的重要生理调节因子。然而,体外研究表明,只有当AT与组织因子(TF)结合时,它才能有效抑制FVIIa。众所周知,循环血液中最多仅含有微量的TF。FVIIa还能结合内皮细胞蛋白C受体(EPCR),但EPCR在AT使FVIIa失活过程中的作用尚不清楚。本研究旨在探讨TF和EPCR在体内AT使FVIIa失活过程中的作用。通过尾静脉给低人TF小鼠(低TF,约为小鼠TF水平的1%)和高人TF小鼠(HTF,约为小鼠TF水平的100%)注射人重组FVIIa(120μg kg-1体重)。在给予rFVIIa后的不同时间间隔,采集血液以测量血浆中FVIIa-AT复合物和rFVIIa抗原水平。尽管小鼠中TF表达存在很大差异,但与低TF小鼠相比,HTF小鼠产生的FVIIa-AT复合物仅多40 - 50%。通过注射脂多糖增加HTF小鼠体内TF的浓度,可使FVIIa-AT复合物水平提高约25%。在野生型、EPCR缺陷型和EPCR过表达型小鼠之间,FVIIa-AT水平未发现显著差异。体外和离体形成的FVIIa-AT复合物水平远低于体内发现的水平。总之,我们的结果表明,循环血液中可能存在的微量TF或正常血管损伤时短暂暴露的血管外TF有助于AT在循环中使FVIIa失活。然而,TF在AT使FVIIa失活过程中的作用似乎较小,血浆、血细胞或血管内皮中存在的其他因素可能在此过程中起主要作用。