Alternatively spliced isoforms of tissue factor pathway inhibitor

被引:42
|
作者
Maroney, Susan A.
Ellery, Paul E.
Mast, Alan E. [1 ,2 ]
机构
[1] Blood Ctr Wisconsin, Blood Res Inst, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
关键词
Tissue factor pathway inhibitor; Blood coagulation; Alternative splicing; Translational regulation; COAGULATION INHIBITOR; FACTOR-X; ANTICOAGULANT ACTIVITY; FACTOR-VIIA; EXPRESSION; SURFACE; PLASMA; DEFICIENCY; LOCALIZATION; PURIFICATION;
D O I
10.1016/j.thromres.2010.01.038
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tissue factor pathway inhibitor (TFPI) is the major regulator of tissue factor (TF)-induced coagulation. It down regulates coagulation by binding to the TF/fVIIa complex in a fXa dependent manner. It is predominantly produced by microvascular endothelial cells, though it is also found in platelets, monocytes, smooth muscle cells, and plasma. Its physiological importance is demonstrated by the embryonic lethality observed in TFPI knockout mice and by the increase in thrombotic burden that occurs when heterozygous TFPI mice are bred with mice carrying genetic risk factors for thrombotic disease, such as factor V Leiden. Multiple TFPI isoforms, termed TFPI alpha, TFPI beta, and TFPI delta in humans and TFPI alpha, TFPI beta, and TFP gamma in mice, have been described, which differ in their domain structure and method for cell surface attachment. A significant functional difference between these isoforms has yet to be described in vivo. Both human and mouse tissues produce, on average, approximately 10 times more TFPI alpha message when compared to that of TFPI beta. Consistent with this finding, several lines of evidence suggest that TFPI alpha is the predominant protein isoform in humans. In contrast, recent work from our laboratory demonstrates that TFPI beta is the major protein isoform produced in adult mice, suggesting that TFPI isoform production is translationally regulated. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:S52 / S56
页数:5
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