Rao L Vijaya Mohan, Pendurthi Usha R
Biomedical Research Division, The University of Texas Health Center at Tyler, 11937 US Highway 271, Tyler, TX 75708, USA.
Arterioscler Thromb Vasc Biol. 2005 Jan;25(1):47-56. doi: 10.1161/01.ATV.0000151624.45775.13. Epub 2004 Nov 29.
How does tissue factor (TF), whose principle role is to support clotting factor VIIa (FVIIa) in triggering the coagulation cascade, affect various pathophysiological processes? One of the answers is that TF interaction with FVIIa not only initiates clotting but also induces cell signaling via activation of G-protein-coupled protease activated receptors (PARs). Recent studies using various cell model systems and limited in vivo systems are beginning to define how TF-VIIa-induced signaling regulates cellular behavior. Signaling pathways initiated by both TF-VIIa protease activation of PARs and phosphorylation of the TF-cytoplasmic domain appear to regulate cellular functions. In the present article, we review the emerging data on the mechanism of TF-mediated cell signaling and how it regulates various cellular responses, with particular focus on TF-VIIa protease-dependent signaling.
组织因子(TF)的主要作用是支持凝血因子VIIa(FVIIa)触发凝血级联反应,它是如何影响各种病理生理过程的呢?答案之一是,TF与FVIIa的相互作用不仅启动凝血,还通过激活G蛋白偶联蛋白酶激活受体(PARs)诱导细胞信号传导。最近使用各种细胞模型系统和有限的体内系统进行的研究开始明确TF-VIIa诱导的信号传导如何调节细胞行为。由TF-VIIa蛋白酶激活PARs和TF胞质结构域磷酸化引发的信号通路似乎都能调节细胞功能。在本文中,我们综述了关于TF介导的细胞信号传导机制及其如何调节各种细胞反应的最新数据,特别关注TF-VIIa蛋白酶依赖性信号传导。