Tissue factor pathway inhibitor deficiency enhances neointimal proliferation and formation in a murine model of vascular remodelling

Ripudamanjit Singh, Shuchong Pan, Cheryl S. Mueske, Tyra A. Witt, Laurel S. Kleppe, Timothy E. Peterson, Noel M. Caplice, Robert D. Simari

Research output: Contribution to journalArticlepeer-review

26 Scopus citations


Tissue factor (TF) is a small-molecular-weight glycoprotein that initiates the extrinsic coagulation pathway but may have important noncoagulation vascular functions as well. Tissue factor pathway inhibitor (TFPI) is a major physiological inhibitor of TF-initiated coagulation. Enhancement of vascular TFPI either by overexpression using gene transfer or delivery of protein to the vessel has been shown to reduce neointimal formation. However, the inherent role of TFPI in this process has not been defined. To do so, we utilized a murine model of vascular remodeling using flow cessation in mice, which are heterozygous for a genetic deletion of the first Kunitz domain of TFPI or wild type littermates. The heterozygotic mice had 50% of wild type TFPI activity in plasma as well as vascular homogenates. To study the effect of TFPI deficiency on neointimal formation, age matched TFPIKI+/- and wildtype littermates underwent unilateral common carotid artery ligation. Mice were sacrificed at 4 weeks and the ligated carotid arteries were analyzed. There was a significantly greater neointima to media ratio and less luminal area in the TFPIKI+/- mice compared to their TFPIKI+/+ littermates. The proliferative index of intimal cells in TFPIKI+/- mice at I week was significantly higher compared to TFPIKI+/+ mice. We conclude that TFPI deficiency enhances neointimal formation and proliferation associated with flow cessation. This suggests that TFPI may regulate vascular remodeling primarily through modulation of neointimal formation.

Original languageEnglish (US)
Pages (from-to)747-751
Number of pages5
JournalThrombosis and Haemostasis
Issue number4
StatePublished - Apr 1 2003


  • Inhibitors
  • Neointima
  • Remodeling
  • Thrombosis
  • Tissue factor

ASJC Scopus subject areas

  • Hematology


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