Borensztajn Keren, Peppelenbosch Maikel P, Spek C Arnold
Department of Cell Biology, University of Groningen, Antonius Deusinglaan 1, NL-9713 EZ, Groningen, The Netherlands.
Trends Mol Med. 2008 Oct;14(10):429-40. doi: 10.1016/j.molmed.2008.08.001. Epub 2008 Sep 4.
Activated factor Xa (FXa) is traditionally known as an important player in the coagulation cascade responsible for thrombin generation. Long considered a passive bystander, it is now evident that FXa exerts direct effects on a wide variety of cell types via activation of its two main receptors, protease-activated receptor-1 (PAR-1) and PAR-2. Recent findings suggest that PAR-2 plays a crucial role in fibro-proliferative diseases such as fibrosis, tissue remodeling and cancer and point towards FXa as the important mediator coordinating the interface between coagulation and disease progression. Here, we provide an overview of the FXa signaling pathways that mediate its effects in pathophysiology and explore the potential therapeutic implications of targeting FXa; in terms of arresting disease progression, the modulation of FXa activity might be more important than the modulation of FVIIa or thrombin.
活化的凝血因子Xa(FXa)传统上被认为是凝血级联反应中负责生成凝血酶的重要参与者。长期以来,它一直被视为被动旁观者,而现在很明显,FXa通过激活其两个主要受体——蛋白酶激活受体-1(PAR-1)和PAR-2,对多种细胞类型发挥直接作用。最近的研究结果表明,PAR-2在诸如纤维化、组织重塑和癌症等纤维增生性疾病中起关键作用,并指出FXa是协调凝血与疾病进展之间界面的重要介质。在此,我们概述了介导FXa在病理生理学中作用的信号通路,并探讨了靶向FXa的潜在治疗意义;就阻止疾病进展而言,调节FXa活性可能比调节FVIIa或凝血酶更为重要。