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

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.

Publication types

  • Review

MeSH terms

  • Animals
  • Hemostasis / drug effects*
  • Humans
  • Lipoproteins / drug effects
  • Lipoproteins / genetics
  • Lipoproteins / metabolism*
  • Protein Processing, Post-Translational
  • RNA Processing, Post-Transcriptional
  • Thrombosis / etiology

Substances

  • Lipoproteins
  • lipoprotein-associated coagulation inhibitor