Thromb Haemost 2006; 96(02): 160-166
DOI: 10.1160/TH06-01-0019
Platelets and Blood Cells
Schattauer GmbH

ADAMTS-13 regulates platelet adhesion under flow

A new method for differentiation between inherited and acquired thrombotic thrombocytopenic purpura
Boris Shenkman
1   Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel-Hashomer, Israel
,
Ulrich Budde
2   Laboratory Prof. Dr. Arndt & Partner, Hamburg, Germany
,
Dorothea Angerhaus
2   Laboratory Prof. Dr. Arndt & Partner, Hamburg, Germany
,
Aharon Lubetsky
1   Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel-Hashomer, Israel
,
Naphtali Savion
4   Goldschleger Eye Research Institute, Tel-Aviv University, Tel-Aviv, Israel
,
Uri Seligsohn
1   Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel-Hashomer, Israel
,
David Varon
3   Coagulation Unit, Hadassah Hebrew University Medical Center, Jerusalem, Israel
› Author Affiliations
Further Information

Publication History

Received 12 January 2006

Accepted after resubmission 07 July 2006

Publication Date:
28 November 2017 (online)

Summary

ADAMTS-13 cleaves large and ultra-large vonWillebrand factor multimers normally secreted by endothelial cells. Severe deficiency of this enzyme leads to thrombotic thrombocytopenic purpura (TTP). We applied the Impact-R system [Cone and plate(let) Analyzer, CPA] to determine optimal conditions for ADAMTS-13 function, to assess it’s activity in TTP patients and to distinguish inheritedTTP (inTTP) from acquiredTTP (acTTP). The role of ADAMTS-13 in platelet adhesion under different conditions was investigated applying recombinant forms of VWF and ADAMTS-13. rVWF was first treated by rADAMTS-13 either in solution or when immobilized on the surface of the well, under static or flow conditions, in the presence or absence of BaCl2. The resulting cleavedVWF fragments were then immobilized and served to assess type 3 von Willebrand disease whole blood platelet adhesion under flow. Maximal effect of the rADAMTS-13 (decrease of platelet adhesion in the absence compared to the presence of BaCl2), was observed when the rVWF was pre-immobilized and the cleavage step took place under flow (85%). Mixing plasma ofTTP patients with normal blood (1:3) yielded a 1.6 to 2-fold increase of platelet adhesion under flow compared to mixing normal plasma with normal blood, at shear rate range of 1,800–2,500s−1. Maximal increase of platelet adhesion was observed under 2,050s−1. Under these conditions, the extent of adhesion was similarly higher in patients with inTTP and acTTP versus control [surface coverage (SC) 14.5 ± 2.8% and 14.6 ± 2.5% vs. 7.4 ± 1.7%, respectively]. ADAMTS-13 activity measured by collagen-binding test was similarly low (4.2 ± 3.8% and 3.5 ± 2.4% vs. 72.2 ± 8.0%, respectively). An inverse correlation between SC and ADAMTS-13 activity was observed in a patient with inTTP assayed eight times during plasma infusion treatment. Addition of BaCl2 to the mixture of TTP plasma and normal whole blood yieldeda decrease in platelet adhesion in inTTP (by 51%) but not in acTTP. The lack of reduction of platelet adhesion in acTTP could presumably be due to the presence of ADAMTS-13 inhibitor in these patients. These results suggest that VWF immobilization and high shear flow yielded optimal conditions for ADAMTS-13 activity, and that introduction of BaCl2 in the Impact-R (CPA) test may be useful for differentiation between inherited and acquired TTP.

 
  • References

  • 1 Furlan M. Willebrand factor: molecular size and functional activity. Ann Hematol 1996; 72: 341-8.
  • 2 Manucci PM, Canciani MT, Forza I. et al. Changes in health and disease of the metalloprotease that cleaves von Willebrand factor. Blood 2001; 98: 2730-5.
  • 3 Dong JF, Whitelock J, Bernardo A. et al. Variations among normal individuals in the cleavage of endothelial-derived ultra-large von Willebrand factor under flow. J Thromb Haemost 2004; 02: 1460-6.
  • 4 George JN. How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Blood 2000; 96: 1223-9.
  • 5 Levy GG, Nichols WC, Lian EC. et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001; 413: 488-94.
  • 6 Tsai HM, Lian EC. Antibodies to von Willebrand factor cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 1998; 339: 1585-9.
  • 7 Hovinga JA, Studt JD, Alberio L. et al. Von Willebrand-cleaving protease (ADAMTS-13) activity determination in the diagnosis of thrombotic microangiopathies: the Swiss experience. Semin Hematol 2004; 41: 75-82.
  • 8 Moake JL, Rudy CK, Troll JH. et al. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 1982; 307: 1432-5.
  • 9 Chow TW, Turner NA, Chintagumpala M. et al. Increased von Willebrand factor binding to platelets in single episode and recurrent types of thrombotic thrombocytopenic purpura. Am J Hematol 1998; 57: 293-302.
  • 10 Moake JL, Turner NA, Stathopoulos NA. et al. Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear-stress-induced platelet aggregation. J Clin Invest 1986; 78: 1456-61.
  • 11 Dong JF, Moake JL, Nolasco L. et al. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. Blood 2002; 100: 4033-9.
  • 12 Obert B, Tout H, Veyradier A. et al. Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF. Thromb Haemost 1999; 82: 1382-5.
  • 13 Gerritsen HE, Turecek PL, Schwarz HP. et al. Assay of von Willebrand factor (VWF)-cleaving protease based on decreased collagen binding affinity of degtadedVWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP). Thromb Haemost 1999; 82: 1386-9.
  • 14 Bohm M, Vigh T, Scharrer I. Evaluation and clinical application ofa new method for measuring activity of von Willebrand factor-cleaving metalloprotease (ADAMTS13). Ann Hematol 2002; 81: 430-5.
  • 15 Shenkman B, Inbal A, Tamarin I. et al. Diagnosis of thrombotic thrombocytopenic purpura based on modulation by patient plasma of normal platelet adhesion under flow condition. Brit J Haematol 2003; 120: 597-604.
  • 16 Varon D, Dardik R, Shenkman B. et al. A new method for quantitative analysis of whole blood platelet interaction with extracellular matrix under flow conditions. Thromb Res 1997; 85: 283-94.
  • 17 Shenkman B, Savion N, Dardik R. et al. Testing of platelet deposition on polystyrene surface under flow conditions by the Cone and Plate(let) Analyzer: role of platelet activation, fibrinogen and von Willebrand factor. Thromb Res 2000; 99: 353-61.
  • 18 Schneppenheim R, Budde U, Obser T. et al. Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease. Blood 2001; 97: 2059-66.
  • 19 Moore JC, Hayward CPM, Warkentin TE. et al. Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders. Blood 2001; 98: 1842-5.
  • 20 Veyradier A, Obert B, Houllier A. et al. Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases. Blood 2001; 98: 1765-72.
  • 21 Tsai HM, Sussman II, Nagel RL. Shear stress enhances the proteolysis of von Willebrand factor in normal plasma. Blood 1994; 83: 2171-9.
  • 22 Siedlecki CA, Lestini BJ, Kottke-Marchant K. et al. Shear-dependent changes in the three-dimensional structure of human von Willebrand factor. Blood 1996; 88: 2939-50.
  • 23 Ruggeri ZM. New insights into the mechanisms of platelet adhesion and aggregation. Semin Hematol 1994; 31: 229-39.
  • 24 Li F, Li ChQ, Moake JL. et al. Shear stress-induced binding of large and unusually large von Willebrand factor to human platelet glycoprotein Iba. Ann Biomed Engineering 2004; 23: 961-9.
  • 25 Ajzenberg N, Denis CV, Veyradier A. et al. Complete defect in VWF-cleaving protease activity associated with increased shear-induced platelet aggregation in thrombotic microangiopathy. Thromb Haemost 2002; 87: 808-11.
  • 26 Galbusera M, Remuzzi A, Binigni A. et al. A novel interpretation of the role of von Willebrand factor in thrombotic microangiopathies based on platelet adhesion studies at high shear rate flow. Am J Kidney Dis 2000; 36: 695-702.
  • 27 Galbusera M, Noris M, Rossi C. et al. Increased fragmentation of von Willebrand factor, due to abnormal cleavage of the subunit, parallels desease activity in recurent hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and discloses predisposition in families. Blood 1999; 94: 610-20.
  • 28 Xie L, Chesterman CN, Hogg PJ. Control of von Willebrand factor multimer size by thrombospondin-1. J Exp Med 2001; 193: 1341-9.
  • 29 Daghistani D, Jimenez JJ, Moake JL. et al. Familial infantile thrombotic thrombocytopenic purpura. J Pediatr Hematol Oncol 1996; 18: 171-4.
  • 30 Savassan S, Taub JW, Buck S. et al. Congenital micriangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease. J Pediatr Hematol Oncol 2001; 23: 364-7.
  • 31 Studt J-D, Boehm M, Budde U. et al. Measurement of von Willebrand factor-cleaving protease (ADAMTS-13) activity in plasma: a multicenter comparison of different assay methods. J Thromb Haemost 2003; 01: 1882-7.