Thromb Haemost 2006; 95(03): 462-468
DOI: 10.1160/TH05-06-0432
Platelets and Blood Cells
Schattauer GmbH

Truncated and microparticle-free soluble tissue factor bound to peripheral monocytes preferentially activate factor VII

Mohammad M. H. Khan*
1   From the Harrison Department of Surgical Research, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
,
Takashi Hattori*
1   From the Harrison Department of Surgical Research, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
,
Stefan Niewiarowski
2   The Sol Sherry Thrombosis Research Center, Hematology Division of the Department of Medicine, Temple University, Philadelphia, Pennsylvania, USA
,
L. Henry Edmunds Jr.
1   From the Harrison Department of Surgical Research, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
,
Robert W. Colman
2   The Sol Sherry Thrombosis Research Center, Hematology Division of the Department of Medicine, Temple University, Philadelphia, Pennsylvania, USA
› Institutsangaben
Financial support: This work was supported by HL 47186 from the National Heart Lung Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Weitere Informationen

Publikationsverlauf

Received 17. Juni 2005

Accepted after resubmission 16. Januar 2006

Publikationsdatum:
29. November 2017 (online)

Summary

Soluble plasma tissue factor (TF) circulates in picomolar concentrations in healthy individuals and increases in a wide spectrum of diseases. This study tests the hypothesis that both truncatedTF (rsTF) or soluble plasmaTF (pTF) in low concentration combine with monocytes or platelets to convert factorVII (fVII) to fVIIa. Both rsTF (33 kDa) and pTF (47 kDa), obtained from pericardial wounds of patients having cardiac surgery using cardiopulmonary bypass (CPB), were studied in association with blood cells and TF-bearing microparticles. Tissue factor was measured by ELISA. RsTF binds to erythrocytes, platelets, mononuclear cells and polymorphoneutrophils. The rate of fVII conversion with rsTF (1–103 nM) is highest with mononuclear cells, less with platelets, minimal with polymorphoneutrophils and undetectable with erythrocytes. Either stimulated or unstimulated mononuclear cells or platelets in the presence of 3.5 pM rsTF or pTF convert fVII (10 nM) to fVIIa, but the amounts of fVIIa produced differ. When leukocytes or platelets are absent, microparticles associated with 3.5 pM TF antigen derived from pericardial wound plasma do not activate fVII. Stimulated mononuclear cells convert nearly all available fVII (10 nM) to fVIIa with 3.5 nM pTF; unstimulated mononuclear cells convert small amounts of fVII with 1 pM rsTF. In all comparisons mononuclear cells more efficiently convert fVII to fVIIa than do platelets. This study shows that stimulated mononuclear cells provide the most efficient platform for activation of rsTF or pTF at low concentrations of TF antigen.

* Drs. Khan and Hattori contributed equally to this project.


+ Drs. Colman and Edmunds are equal senior authors.


 
  • References

  • 1 Koyama T, Nishida K, Ohdama S. et al. Determination of plasma tissue factor antigen and its clinical significance. Br J Haematol 1994; 87: 343-7.
  • 2 Giesen PLA, Rauch U, Bohrmann B. et al. Bloodborne tissue factor: another view of thrombosis. Proc Natl Acad Sci 1999; 96: 2311-5.
  • 3 Giesen PLA, Nemerson Y. Tissue factor on the loose. Sem Thromb Hemost 2000; 26: 379-84.
  • 4 Morrissey JH. Tissure factor: in at the start and the finish?. J Thromb Haemost 2003; 01: 878-80.
  • 5 Eilertsen K-E, Osterud B. Tissue factor: (patho)physiology and cellular biology. Blood Coagul Fibrinolysis 2004; 15: 521-38.
  • 6 Bogdanov VY, Balasubramanian V, Hathcock J. et al. Alternatively spliced human tissue factor: a circulating, soluble thrombogenic protein. Nat Med 2003; 04: 458-62.
  • 7 Sturk-Maquelin KN, Nieuwland R. Romijn FPHTM. et al. Proand non-coagulant forms of noncell-bound tissue factor in vivo. J Thromb Haemost 2003; 01: 1920-6.
  • 8 Muller I, Klocke A, Ales M. et al. Intravascular tissue factor initiates coagulation via circulating microvesicles and platelets. FASEB 2003; 17: 476-8.
  • 9 Hattori T, Khan MMH, Colman RW. et al. Plasma tissue factor plus activated peripheral mononuclear cells activate factors VII and X in cardiac surgical wounds. J Am Coll Cardiol 2005; 46: 707-13.
  • 10 Gregory SA, Morrissey JH, Edgington TS. Regulation of tissue factor gene expression in the monocyte procoagulant response to endotoxin. Mol Cell Biol 1989; 09: 2752-5.
  • 11 Parry GC, Mackman N. Transcriptional regulation of tissue factor expression in human endothelial cells. Arterioscler Thromb Vasc Biol 1995; 15: 612-21.
  • 12 Osterud B, Rao LV, Olsen JO. Induction of tissue factor expression in whole blood: lack of evidence for the presence of tissue factor expression in granulocytes. Thromb Haemost 2000; 83: 861-7.
  • 13 Zillmann A, Luther T, Muller I. et al. Platelet-associated tissue factor contributes to the collagen-triggered activation of blood coagulation. Biochem Biophys Res Com 2001; 281: 603-9.
  • 14 Engelmann B, Luther T, Muller I. Intravascular tissue factor pathway - a model for rapid initiation of coagulation with the blood. Thromb Haemost 2003; 89: 3-8.
  • 15 Rauch U, Bonderman D, Bohmann B. et al. Transfer of tissue factor from leukocytes to platelets is mediated by CD15 and tissue factor. Blood 2000; 96: 170-5.
  • 16 Siddiqui FA, Desai H, Amirkhosravi A. et al. The presence and release of tissue factor from human platelets. Platelets 2002; 13: 247-53.
  • 17 Berckmans RJ, Nieuwalnd R, Boing AN. et al. Cell-derived microparticles circulate in healthy humans and support low grade thrombin generation. Thromb Haemost 2001; 85: 639-46.
  • 18 Biro E, Sturk-Maquelin KN, Vogel GMT. et al. Human cell-derived microparticles promote thrombus formation in vivo ina tissue factor-dependent manner. J Thromb Haemost 2003; 01: 2561-8.
  • 19 Nieuwland R, Berckmans RJ, McGregor S. et al. Cellular origin and procoagulant properties of microparticles in meningococcal sepsis. Blood 2000; 95: 930-5.
  • 20 Joop K, Berckmans RJ, Nieuwland R. et al. Microparticles from patients with multiple organ dysfunction syndrome and sepsis support coagulation through multiple mechanisms. Thromb Haemost 2001; 85: 810-20.
  • 21 Philippou H, Adami A, Davidson SJ. et al. Tissue factor is rapidly elevated in plasma collected from the pericardial cavity during cardiopulmonary bypass. Thromb Haemost 2000; 84: 124-8.
  • 22 Nieuwland R, Berckmans RJ, Rotteveel-Eijkman R. et al. Cell-derived microparticles generated in patients during cardiopulmonary bypass are highly procoagulant. Circulation 1997; 96: 3534-41.
  • 23 Shibamiya A, Tabuchi N, Chung J. et al. Formation of tissue factor-bearing leukocytes during and after cardiopulmonary bypass. Thromb Haemost 2004; 92: 124-31.
  • 24 Fujimi S, Ogura H, Tanaka H. et al. Increased production of leukocyte microparticles with enhanced expression of adhesion molecules from activated polymorphonuclear leukocytes in severely injured patients. J Trauma 2003; 54: 114-9.
  • 25 Sase T, Wada H, Kamikura Y. et al. Tissue factor messenger RNA levels in leukocytes compared with tissue factor antigens in plasma from patients in hypercoagulable state caused by various diseases. Thromb Haemost 2004; 92: 132-9.
  • 26 Annex BH, Denning SM, Channon KM. et al. Differential expression of tissue factor protein in directional atherectomy specimens from patients with stable and unstable coronary syndromes. Circulation 1995; 91: 619-22.
  • 27 Mallat Z, Benamer H, Hugel B. et al. Elevated levels of shed membrane microparticles with procoagulant potential in the peripheral circulating blood of patients with acute coronary syndromes. Circulation 2000; 101: 841-3.
  • 28 Suefuji H, Ogawa H, Yasue H. et al. Increased plasma tissue factor levels in acute myocardial infarction. Am Heart J 1997; 134: 253-9.
  • 29 Soejima H, Ogawa H, Yasue H. et al. Heightened tissue factor associated with tissue factor pathway inhibitor and prognosis in patients with unstable angina. Circulation 1999; 99: 2908-13.
  • 30 Diamant M, Nieuwland R, Pablo RF. et al. Elevated numbers of tissue-factor exposing microparticles correlate with components of the metabolic syndrome in uncomplicated type 2 diabetes mellitus. Circulation 2002; 106: 2442-7.
  • 31 Mustard JF, Perry DW, Ardlie NG. et al. Preparation of suspensions of washed platelets from humans. Br J Haematol 1972; 22: 193-204.
  • 32 English D, Anderson BR. Single-step separation of red blood cells, granulocytes and mononuclear leukocytes on discontinuous density gradient of ficoll-hystopaque. J Immunol Methods 1974; 05: 249.
  • 33 Boyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of mononuclear cells by one centrifugation and of granulocytes by combining centrifugation and sedimentation at1 g. Scand J Clin Lab Invest 1968; 97: 77-88.
  • 34 Neuenschwander PF, Morrissey JH. Deletion of the membrane anchoring region of tissue factor abolishes autoactivation of factor VII but not cofactor function. J Biol Chem 1992; 267: 14477-82.
  • 35 Ryan EJ, Marshall AJ, Magaletti D. et al. Dendritic cell-associated lectin-1: a novel dendritic cell-associated, C-type lectin-like molecule enhances T cell secretion of IL-4. J Immunol 2002; 169: 5638-48.
  • 36 Ruf W, Rehemtulla A, Edgington TS. Phospholipid-independent and -dependent interactions required for tissue factor receptor and cofactor function. J Biol Chem 1991; 266: 2158-66.
  • 37 Morrissey JH, Revak D, Tejada P. et al. Resolution of monomeric and heterodimeric forms of tissue factor, the high-affinity cellular receptor for factor VII. Thromb Res 1988; 50: 481-93.
  • 38 Chung JH, Gikakis N, Rao AK. et al. Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass. Circulation 1996; 93: 2014-8.