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组织因子:凝血与细胞信号交汇的枢纽

Tissue factor at the crossroad of coagulation and cell signaling.

机构信息

Center for Thrombosis and Hemostasis, Johannes Gutenberg University Medical Center, Mainz, Germany.

National Scientific and Technical Research Council (CONICET) and National University of Tucumán, Tucumán, Argentina.

出版信息

J Thromb Haemost. 2018 Oct;16(10):1941-1952. doi: 10.1111/jth.14246. Epub 2018 Aug 16.

Abstract

The tissue factor (TF) pathway plays a central role in hemostasis and thrombo-inflammatory diseases. Although structure-function relationships of the TF initiation complex are elucidated, new facets of the dynamic regulation of TF's activities in cells continue to emerge. Cellular pathways that render TF non-coagulant participate in signaling of distinct TF complexes with associated proteases through the protease-activated receptor (PAR) family of G protein-coupled receptors. Additional co-receptors, including the endothelial protein C receptor (EPCR) and integrins, confer signaling specificity by directing subcellular localization and trafficking. We here review how TF is switched between its role in coagulation and cell signaling through thiol-disulfide exchange reactions in the context of physiologically relevant lipid microdomains. Inflammatory mediators, including reactive oxygen species, activators of the inflammasome, and the complement cascade play pivotal roles in TF procoagulant activation on monocytes, macrophages and endothelial cells. We furthermore discuss how TF, intracellular ligands, co-receptors and associated proteases are integrated in PAR-dependent cell signaling pathways controlling innate immunity, cancer and metabolic inflammation. Knowledge of the precise interactions of TF in coagulation and cell signaling is important for understanding effects of new anticoagulants beyond thrombosis and identification of new applications of these drugs for potential additional therapeutic benefits.

摘要

组织因子(TF)途径在止血和血栓炎症性疾病中发挥核心作用。尽管 TF 起始复合物的结构-功能关系已经阐明,但细胞中 TF 活性的动态调节的新方面仍在不断出现。使 TF 无凝血活性的细胞途径通过蛋白酶激活受体(PAR)家族的 G 蛋白偶联受体参与不同 TF 复合物及其相关蛋白酶的信号转导。其他共受体,包括内皮蛋白 C 受体(EPCR)和整合素,通过指导细胞内定位和运输来赋予信号转导特异性。我们在此综述了 TF 如何通过生理相关的脂质微区中的巯基-二硫键交换反应在凝血和细胞信号转导之间转换。炎症介质,包括活性氧、炎性体激活剂和补体级联,在单核细胞、巨噬细胞和内皮细胞上 TF 促凝血激活中发挥关键作用。我们还讨论了 TF、细胞内配体、共受体和相关蛋白酶如何整合在依赖 PAR 的细胞信号通路中,以控制先天免疫、癌症和代谢性炎症。了解 TF 在凝血和细胞信号转导中的精确相互作用对于理解新型抗凝剂在血栓形成以外的作用以及确定这些药物在潜在治疗益处方面的新应用非常重要。

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