Endothelial PAI-1 (plasminogen activator inhibitor-1) blocks the intrinsic pathway of coagulation, inducing the clearance and degradation of FXIA (activated factor XI)

Cristina Puy, Anh T.P. Ngo, Jiaqing Pang, Ravi S. Keshari, Matthew W. Hagen, Monica T. Hinds, David Gailani, András Gruber, Florea Lupu, Owen J.T. McCarty

Research output: Contribution to journalArticle

4 Scopus citations


Objective-Activation of coagulation FXI (factor XI) by FXIIa (activated factor XII) is a prothrombotic process. The endothelium is known to play an antithrombotic role by limiting thrombin generation and platelet activation. It is unknown whether the antithrombotic role of the endothelium includes sequestration of FXIa (activated factor XI) activity. This study aims to determine the role of endothelial cells (ECs) in the regulation of the intrinsic pathway of coagulation. Approach and Results-Using a chromogenic assay, we observed that human umbilical veins ECs selectively blocked FXIa yet supported kallikrein and FXIIa activity. Western blotting and mass spectrometry analyses revealed that FXIa formed a complex with endothelial PAI-1 (plasminogen activator inhibitor-1). Blocking endothelial PAI-1 increased the cleavage of a chromogenic substrate by FXIa and the capacity of FXIa to promote fibrin formation in plasma. Western blot and immunofluorescence analyses showed that FXIa-PAI-1 complexes were either released into the media or trafficked to the early and late endosomes and lysosomes of ECs. When baboons were challenged with Staphylococcus aureus to induce a prothrombotic phenotype, an increase in circulating FXIa-PAI-1 complex levels was detected by ELISA within 2 to 8 hours postchallenge. Conclusions-PAI-1 forms a complex with FXIa on ECs, blocking its activity and inducing the clearance and degradation of FXIa. Circulating FXIa-PAI-1 complexes were detected in a baboon model of S. aureus sepsis. Although ECs support kallikrein and FXIIa activity, inhibition of FXIa by ECs may promote the clearance of intravascular FXIa.

Original languageEnglish (US)
Pages (from-to)1390-1401
Number of pages12
JournalArteriosclerosis, thrombosis, and vascular biology
Issue number7
StatePublished - Jan 1 2019



  • Endothelium
  • Fibrin
  • Kallikrein
  • Platelet activation
  • Thrombin

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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