Tissue factor non-coagulant signaling - molecular mechanisms and biological consequences with a focus on cell migration and apoptosis

被引:48
作者
Aberg, M. [1 ]
Siegbahn, A. [1 ]
机构
[1] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
apoptosis; cell migration; cell signaling; factorVIIa; protease-activated receptor; tissue factor; PERIPHERAL-BLOOD MONOCYTES; CANINE KIDNEY-CELLS; FACTOR-VIIA; FACTOR EXPRESSION; CYTOPLASMIC DOMAIN; UP-REGULATION; FACTOR-XA; KINASE PATHWAY; P-SELECTIN; ACTIVATION;
D O I
10.1111/jth.12156
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Tissue factor (TF), a transmembrane glycoprotein, is the main initiator of the blood coagulation cascade. TF is also recognized as a true signaling receptor. There is accumulating evidence that the downstream signaling effects of the TF complexes are transduced by several mechanisms, including: activation of protease-activated receptor (PAR)-1 and PAR-2, and the PAR-dependent pathways, via the TF cytoplasmic domain and by transactivation of receptor tyrosine kinases. Triggering of signaling cascades such as the mitogen-activated protein kinase and phosphoinositide 3-kinase/AKT pathways couples TF to a multitude of functions within the cell, such as proliferation, cell migration, and survival. Thus, TF has a Janus face; on the one hand, it has vital life-maintaining functions, and on the other it has harmful effects, exemplified by inflammation, the acute coronary syndromes, and cancer. TF mediates a broad spectrum of signaling mechanisms. Learning more about these different mechanisms/pathways will lead to new treatment strategies, which can ultimately be personalized.
引用
收藏
页码:817 / 825
页数:9
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