Thromb Haemost 2022; 122(09): 1502-1512
DOI: 10.1055/s-0042-1744379
Cellular Haemostasis and Platelets

Platelet Activation via Glycoprotein VI Initiates Thrombin Generation: A Potential Role for Platelet-Derived Factor IX?

Li Li
1   Department of Platelet Pathophysiology, Synapse Research Institute, Maastricht, The Netherlands
2   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
,
Mark Roest
1   Department of Platelet Pathophysiology, Synapse Research Institute, Maastricht, The Netherlands
2   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
,
Joost C. M. Meijers
3   Department of Molecular Hematology, Sanquin Research, Amsterdam, The Netherlands
4   Department of Experimental Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands
,
Bas de Laat
1   Department of Platelet Pathophysiology, Synapse Research Institute, Maastricht, The Netherlands
2   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
,
Rolf T. Urbanus
5   Van Creveldkliniek, University Medical Center Utrecht, Utrecht, The Netherlands
,
Philip G. de Groot
1   Department of Platelet Pathophysiology, Synapse Research Institute, Maastricht, The Netherlands
,
1   Department of Platelet Pathophysiology, Synapse Research Institute, Maastricht, The Netherlands
2   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
› Author Affiliations
Funding Li Li is supported by a scholarship (No. 201706230245) from the China Scholarship Council.

Abstract

Collagen triggers coagulation via activation of factor (F) XII. In a platelet-rich environment, collagen can also trigger coagulation independently of FXII. We studied a novel mechanism of coagulation initiation via collagen-dependent platelet activation using thrombin generation (TG) in platelet-rich plasma. Collagen-induced coagulation is minimally affected by active-site inactivated FVIIa, anti-FVII antibodies, or FXIIa inhibition (corn trypsin inhibitor). Activation of platelets via specific glycoprotein (GP) VI agonists initiates TG, FX activation, and fibrin formation. To determine the platelet-derived trigger of coagulation, we systematically reconstituted factor-deficient plasmas with washed platelets. TG triggered by GPVI-activated platelets was significantly affected in FIX- and FVIII-deficient plasma but not in FVII- and FXII-deficient plasma. In a purified system composed of FX and FVIII, we observed that absence of FIX was compensated by GPVI-activated platelets, which could be inhibited by an anti-FIX antibody, suggesting FIXa activity from activated platelets. Furthermore, with the addition of FVIII in FIX-deficient plasma, TG induced by GPVI-activated platelets was restored, and was inhibited by the anti-FIX antibody. In conclusion, GPVI-activated platelets initiate TG, probably via platelet-derived FIXa activity.

Author Contributions

Contribution: L.L., D.H., M.R., R.T.U., P.G.d.G., and B.d.L. were involved in the conception and design of the experiments. J.C.M.M. was involved in the design of the experiments and provided essential reagents. L.L. performed the experiments. L.L. and D.H. interpreted the data and drafted the manuscript. M.R., P.G.d.G., B.d.L., R.T.U., and J.C.M.M. critically revised the manuscript. All authors approved the final version of the article.


Supplementary Material



Publication History

Received: 27 September 2021

Accepted: 03 February 2022

Article published online:
05 May 2022

© 2022. Thieme. All rights reserved.

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  • References

  • 1 Jung SM, Moroi M, Soejima K. et al. Constitutive dimerization of glycoprotein VI (GPVI) in resting platelets is essential for binding to collagen and activation in flowing blood. J Biol Chem 2012; 287 (35) 30000-30013
  • 2 Smethurst PA, Onley DJ, Jarvis GE. et al. Structural basis for the platelet-collagen interaction: the smallest motif within collagen that recognizes and activates platelet glycoprotein VI contains two glycine-proline-hydroxyproline triplets. J Biol Chem 2007; 282 (02) 1296-1304
  • 3 Knight CG, Morton LF, Onley DJ. et al. Collagen-platelet interaction: Gly-Pro-Hyp is uniquely specific for platelet Gp VI and mediates platelet activation by collagen. Cardiovasc Res 1999; 41 (02) 450-457
  • 4 Knight CG, Morton LF, Peachey AR, Tuckwell DS, Farndale RW, Barnes MJ. The collagen-binding A-domains of integrins alpha(1)beta(1) and alpha(2)beta(1) recognize the same specific amino acid sequence, GFOGER, in native (triple-helical) collagens. J Biol Chem 2000; 275 (01) 35-40
  • 5 van der Meijden PE, Munnix IC, Auger JM. et al. Dual role of collagen in factor XII-dependent thrombus formation. Blood 2009; 114 (04) 881-890
  • 6 Heemskerk JW, Kuijpers MJ, Munnix IC, Siljander PR. Platelet collagen receptors and coagulation. A characteristic platelet response as possible target for antithrombotic treatment. Trends Cardiovasc Med 2005; 15 (03) 86-92
  • 7 Emsley J, Knight CG, Farndale RW, Barnes MJ, Liddington RC. Structural basis of collagen recognition by integrin alpha2beta1. Cell 2000; 101 (01) 47-56
  • 8 Nieswandt B, Watson SP. Platelet-collagen interaction: is GPVI the central receptor?. Blood 2003; 102 (02) 449-461
  • 9 Watson SP, Auger JM, McCarty OJ, Pearce AC. GPVI and integrin alphaIIb beta3 signaling in platelets. J Thromb Haemost 2005; 3 (08) 1752-1762
  • 10 Gibbins JM, Okuma M, Farndale R, Barnes M, Watson SP. Glycoprotein VI is the collagen receptor in platelets which underlies tyrosine phosphorylation of the Fc receptor gamma-chain. FEBS Lett 1997; 413 (02) 255-259
  • 11 Jung SM, Tsuji K, Moroi M. Glycoprotein (GP) VI dimer as a major collagen-binding site of native platelets: direct evidence obtained with dimeric GPVI-specific Fabs. J Thromb Haemost 2009; 7 (08) 1347-1355
  • 12 Mackman N. Role of tissue factor in hemostasis, thrombosis, and vascular development. Arterioscler Thromb Vasc Biol 2004; 24 (06) 1015-1022
  • 13 Gibbins JM. Platelet adhesion signalling and the regulation of thrombus formation. J Cell Sci 2004; 117 (Pt 16): 3415-3425
  • 14 Broos K, Feys HB, De Meyer SF, Vanhoorelbeke K, Deckmyn H. Platelets at work in primary hemostasis. Blood Rev 2011; 25 (04) 155-167
  • 15 Versteeg HH, Heemskerk JW, Levi M, Reitsma PH. New fundamentals in hemostasis. Physiol Rev 2013; 93 (01) 327-358
  • 16 Müller F, Mutch NJ, Schenk WA. et al. Platelet polyphosphates are proinflammatory and procoagulant mediators in vivo. Cell 2009; 139 (06) 1143-1156
  • 17 Tracy PB, Eide LL, Bowie EJ, Mann KG. Radioimmunoassay of factor V in human plasma and platelets. Blood 1982; 60 (01) 59-63
  • 18 Marx G, Korner G, Mou X, Gorodetsky R. Packaging zinc, fibrinogen, and factor XIII in platelet alpha-granules. J Cell Physiol 1993; 156 (03) 437-442
  • 19 Chesney CM, Pifer D, Colman RW. Subcellular localization and secretion of factor V from human platelets. Proc Natl Acad Sci U S A 1981; 78 (08) 5180-5184
  • 20 Romp KG, Monroe DM, Hoffman M. Platelets contain releasable coagulation factor IX antigen. Blood Coagul Fibrinolysis 1993; 4 (06) 905-910
  • 21 Achison M, Joel C, Hargreaves PG, Sage SO, Barnes MJ, Farndale RW. Signals elicited from human platelets by synthetic, triple helical, collagen-like peptides. Blood Coagul Fibrinolysis 1996; 7 (02) 149-152
  • 22 Polgár J, Clemetson JM, Kehrel BE. et al. Platelet activation and signal transduction by convulxin, a C-type lectin from Crotalus durissus terrificus (tropical rattlesnake) venom via the p62/GPVI collagen receptor. J Biol Chem 1997; 272 (21) 13576-13583
  • 23 Reyes CD, García AJ. Engineering integrin-specific surfaces with a triple-helical collagen-mimetic peptide. J Biomed Mater Res A 2003; 65 (04) 511-523
  • 24 Hemker HC, Giesen P, Al Dieri R. et al. Calibrated automated thrombin generation measurement in clotting plasma. Pathophysiol Haemost Thromb 2003; 33 (01) 4-15
  • 25 Korporaal SJ, Van Eck M, Adelmeijer J. et al. Platelet activation by oxidized low density lipoprotein is mediated by CD36 and scavenger receptor-A. Arterioscler Thromb Vasc Biol 2007; 27 (11) 2476-2483
  • 26 Al Dieri R, Bloemen S, Kelchtermans H, Wagenvoord R, Hemker HC. A new regulatory function of activated factor V: inhibition of the activation by tissue factor/factor VII(a) of factor X. J Thromb Haemost 2013; 11 (03) 503-511
  • 27 Weitz JI, Fredenburgh JC. Platelet polyphosphate: the long and the short of it. Blood 2017; 129 (12) 1574-1575
  • 28 Smith SA, Mutch NJ, Baskar D, Rohloff P, Docampo R, Morrissey JH. Polyphosphate modulates blood coagulation and fibrinolysis. Proc Natl Acad Sci U S A 2006; 103 (04) 903-908
  • 29 Faxälv L, Boknäs N, Ström JO. et al. Putting polyphosphates to the test: evidence against platelet-induced activation of factor XII. Blood 2013; 122 (23) 3818-3824
  • 30 Verhoef JJ, Barendrecht AD, Nickel KF. et al. Polyphosphate nanoparticles on the platelet surface trigger contact system activation. Blood 2017; 129 (12) 1707-1717
  • 31 Kearney KJ, Butler J, Posada OM. et al. Kallikrein directly interacts with and activates Factor IX, resulting in thrombin generation and fibrin formation independent of Factor XI. Proc Natl Acad Sci U S A 2021; 118 (03) 118
  • 32 Burkhart JM, Vaudel M, Gambaryan S. et al. The first comprehensive and quantitative analysis of human platelet protein composition allows the comparative analysis of structural and functional pathways. Blood 2012; 120 (15) e73-e82
  • 33 Swieringa F, Spronk HMH, Heemskerk JWM, van der Meijden PEJ. Integrating platelet and coagulation activation in fibrin clot formation. Res Pract Thromb Haemost 2018; 2 (03) 450-460
  • 34 Gailani D, Zivelin A, Sinha D, Walsh PN. Do platelets synthesize factor XI?. J Thromb Haemost 2004; 2 (10) 1709-1712
  • 35 Hsu T-C, Shore SK, Seshsmma T, Bagasra O, Walsh PN. Molecular cloning of platelet factor XI, an alternative splicing product of the plasma factor XI gene. J Biol Chem 1998; 273 (22) 13787-13793
  • 36 Podmore A, Smith M, Savidge G, Alhaq A. Real-time quantitative PCR analysis of factor XI mRNA variants in human platelets. J Thromb Haemost 2004; 2 (10) 1713-1719
  • 37 Martincic D, Kravtsov V, Gailani D. Factor XI messenger RNA in human platelets. Blood 1999; 94 (10) 3397-3404
  • 38 Zucker M, Hauschner H, Seligsohn U, Rosenberg N. Platelet factor XI: intracellular localization and mRNA splicing following platelet activation. Blood Cells Mol Dis 2018; 69: 30-37
  • 39 Weeterings C, de Groot PG, Adelmeijer J, Lisman T. The glycoprotein Ib-IX-V complex contributes to tissue factor-independent thrombin generation by recombinant factor VIIa on the activated platelet surface. Blood 2008; 112 (08) 3227-3233
  • 40 Butenas S, Orfeo T, Gissel MT, Brummel KE, Mann KG. The significance of circulating factor IXa in blood. J Biol Chem 2004; 279 (22) 22875-22882
  • 41 Prior SM, Mann KG, Freeman K, Butenas S. Continuous thrombin generation in whole blood: New applications for assessing activators and inhibitors of coagulation. Anal Biochem 2018; 551: 19-25
  • 42 Zhang G, Shi Q, Fahs SA, Kuether EL, Walsh CE, Montgomery RR. Factor IX ectopically expressed in platelets can be stored in alpha-granules and corrects the phenotype of hemophilia B mice. Blood 2010; 116 (08) 1235-1243
  • 43 Maynard DM, Heijnen HF, Horne MK, White JG, Gahl WA. Proteomic analysis of platelet alpha-granules using mass spectrometry. J Thromb Haemost 2007; 5 (09) 1945-1955
  • 44 Maynard DM, Heijnen HF, Gahl WA, Gunay-Aygun M. The α-granule proteome: novel proteins in normal and ghost granules in gray platelet syndrome. J Thromb Haemost 2010; 8 (08) 1786-1796
  • 45 Cremer SE, Catalfamo JL, Goggs R, Seemann SE, Kristensen AT, Brooks MB. Proteomic profiling of the thrombin-activated canine platelet secretome (CAPS). PLoS One 2019; 14 (11) e0224891
  • 46 Ramstrom S, O'Neill S, Dunne E, Kenny D. Annexin V binding to platelets is agonist, time and temperature dependent. Platelets 2010; 21 (04) 289-296
  • 47 Heemskerk JW, Mattheij NJ, Cosemans JM. Platelet-based coagulation: different populations, different functions. J Thromb Haemost 2013; 11 (01) 2-16
  • 48 Heemskerk JW, Bevers EM, Lindhout T. Platelet activation and blood coagulation. Thromb Haemost 2002; 88 (02) 186-193