Thromb Haemost 2018; 118(06): 990-1000
DOI: 10.1055/s-0038-1642031
Coagulation and Fibrinolysis
Schattauer GmbH Stuttgart

Tissue Factor Coagulant Activity is Regulated by the Plasma Membrane Microenvironment

Yuanjie Yu*
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
,
Anita N. Böing*
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
,
Chi M. Hau
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
,
Najat Hajji
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
,
Wolfram Ruf
2   Department of Immunology and Microbial Science, Scripps Research Institute, La Jolla, California, United States
3   Center for Thrombosis and Hemostasis, Johannes Gutenberg Medical Center, Mainz, Germany
,
Auguste Sturk
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
,
Rienk Nieuwland
1   Laboratory of Clinical Chemistry, and Vesicle Observation Centre, Academic Medical Centre of the University of Amsterdam, Amsterdam, The Netherlands
› Author Affiliations
Further Information

Publication History

30 October 2017

11 March 2018

Publication Date:
21 April 2018 (online)

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Abstract

Background Tissue factor (TF) can be present in a non-coagulant and coagulant form. Whether the coagulant activity is affected by the plasma membrane microenvironment is unexplored.

Objective This article studies the presence and coagulant activity of human TF in plasma membrane micro-domains.

Methods Plasma membranes were isolated from human MIA PaCa2 cells, MDA-MB-231 cells and human vascular smooth muscle cells by Percoll gradient ultracentrifugation after cell disruption. Plasma membranes were fractionated by OptiPrep gradient ultracentrifugation, and the presence of TF, flotillin, caveolin, clathrin, protein disulphide isomerase (PDI), TF pathway inhibitor (TFPI) and phosphatidylserine (PS) were determined.

Results Plasma membranes contain two detergent-resistant membrane (DRM) compartments differing in density and biochemical composition. High-density DRMs (DRM-H) have a density (ρ) of 1.15 to 1.20 g/mL and contain clathrin, whereas low-density DRMs (DRM-L) have a density between 1.09 and 1.13 g/mL and do not contain clathrin. Both DRMs contain TF, flotillin and caveolin. PDI is detectable in DRM-H, TFPI is not detectable in either DMR-H or DRM-L and PS is detectable in DRM-L. The DRM-H-associated TF (> 95% of the TF antigen) lacks detectable coagulant activity, whereas the DRM-L-associated TF triggers coagulation. This coagulant activity is inhibited by lactadherin and thus PS-dependent, but seemed insensitive to 16F16, an inhibitor of PDI.

Conclusion Non-coagulant and coagulant TF are present within different types of DRMs in the plasma membrane, and the composition of these DRMs may affect the TF coagulant activity.

* These authors contributed equally to the work.


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