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Post-transcriptional, post-translational and pharmacological regulation of tissue factor pathway inhibitor.

作者信息

Subramaniam Saravanan, Kanse Sandip M, Kothari Hema, Reinhardt Christoph, Fletcher Craig

机构信息

Blood Research Institute, BloodCenter of Wisconsin, Milwaukee.

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Blood Coagul Fibrinolysis. 2018 Dec;29(8):668-682. doi: 10.1097/MBC.0000000000000775.

Abstract

: Tissue factor (TF) pathway inhibitor (TFPI) is an endogenous natural anticoagulant that readily inhibits the extrinsic coagulation initiation complex (TF-FVIIa-Xa) and prothrombinase (FXa, FVa and calcium ions). Alternatively, spliced TFPI isoforms (α, β and δ) are expressed by vascular and extravascular cells and regulate thrombosis and haemostasis, as well as cell signalling functions of TF complexes via protease-activated receptors (PARs). Proteolysis of TFPI plays an important role in regulating physiological roles of the TF pathway in host defense and possibly haemostasis. Elimination of TFPI inhibition has therefore been proposed as an approach to improve haemostasis in haemophilia patients. In this review, we focus on posttranscription and translational modification of TFPI and its function in thrombosis and how pharmacological inhibitors and endogenous proteases interfere with TFPI and alter haemostasis.

摘要

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