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组织因子途径抑制剂(TFPI)——最新进展

Tissue factor pathway inhibitor (TFPI)--an update.

作者信息

Sandset P M

机构信息

Haematology Research Laboratory, Ullevaal University Hospital, Oslo, Norway.

出版信息

Haemostasis. 1996 Oct;26 Suppl 4:154-65. doi: 10.1159/000217293.

Abstract

There is compelling experimental evidence that tissue factor pathway inhibitor (TFPI) exerts important role(s) as a natural anticoagulant. Immunodepletion of TFPI lowers the treshold by which tissue factor (TF) can induce disseminated intravascular coagulation. Conversely, infusion of recombinant TFPI protects against thrombosis and disseminated intravascular coagulation in numerous experimental models. Since TFPI mutants associated with thrombosis have not yet been identified, a definite role of TFPI in coagulation is yet to be assigned. Current research on TFPI is mainly focused on the cell biology of TFPI, on the contribution of TFPI to the anticoagulant action of heparins, and on the role of lipoprotein-associated TFPI. TFPI is produced constitutively in endothelial cells, and is to a great extent bound to its surface. The binding molecule(s) have not yet been characterized, but TFPI is rapidly released by heparin and other negatively charged ions. In other cell lines degradation of TFPI is mediated by the low density lipoprotein receptor-related protein, which may be important for its clearance. In plasma, TFPI contributes strongly to the postheparin anticoagulant effect seen in dilute prothrombin time assays. The effect is probably mediated by redistribution of TFPI. Moreover, in the presence of heparin, antithrombin and TFPI cooperate to inhibit activation of coagulation. Antithrombin abrogates activation of factor VII bound to TF, whereas TFPI inhibits factor VIIa/TF complexes formed. The role of lipoprotein associated TFPI is still essentially unknown, but may play an important role in atherosclerosis.

摘要

有令人信服的实验证据表明,组织因子途径抑制物(TFPI)作为一种天然抗凝剂发挥着重要作用。去除TFPI的免疫耗竭会降低组织因子(TF)诱导弥散性血管内凝血的阈值。相反,在众多实验模型中,输注重组TFPI可预防血栓形成和弥散性血管内凝血。由于尚未鉴定出与血栓形成相关的TFPI突变体,TFPI在凝血中的明确作用尚待确定。目前对TFPI的研究主要集中在TFPI的细胞生物学、TFPI对肝素抗凝作用的贡献以及脂蛋白相关TFPI的作用上。TFPI在内皮细胞中组成性产生,并在很大程度上与内皮细胞表面结合。尚未对结合分子进行表征,但TFPI可被肝素和其他带负电荷的离子迅速释放。在其他细胞系中,TFPI的降解由低密度脂蛋白受体相关蛋白介导,这可能对其清除很重要。在血浆中,TFPI对稀释凝血酶原时间测定中所见的肝素后抗凝作用有很大贡献。这种作用可能是由TFPI的重新分布介导的。此外,在肝素存在的情况下,抗凝血酶和TFPI协同抑制凝血激活。抗凝血酶消除与TF结合的因子VII的激活,而TFPI抑制形成的因子VIIa/TF复合物。脂蛋白相关TFPI的作用仍基本未知,但可能在动脉粥样硬化中起重要作用。

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