Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions

Blood

Volumn 97, Issue 1, 2001, Pages 162-168

  Dong, Jing Fei ^b   Berndt, Michael C ^a   Schade, Alicia ^c   Mclntire, Larry V ^c   Andrews, Robert K ^c   López, José A ^c  

^a BAKER IDI HEART AND DIABETES INSTITUTE   (Australia)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 9; BOTROCETIN; GLYCOPROTEIN IB; RISTOCETIN; VON WILLEBRAND FACTOR;

ANIMAL CELL; ARTICLE; HEMOSTASIS; HYDRODYNAMICS; NONHUMAN; PRIORITY JOURNAL; SHEAR STRESS; THROMBOCYTE AGGREGATION; THROMBOCYTE MEMBRANE; THROMBOSIS;

EID: 0035174016     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V97.1.162     Document Type: Article

References (39)

1. Developing relationships: Arterial platelet adhesion, glycoprotein Ib, and leucine-rich glycoproteins
2. Structure function of von Willebrand factor
3. Platelets and shear stress
4. Identification of aspartic acid 514 through glutamic acid 542 as a glycoprotein Ib-IX complex receptor recognition sequence in von Willebrand factor: Mechanism of modulation of von Willebrand factor by ristocetin and botrocetin
5. Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib
6. A role for von Willebrand factor proline residues 702-704 in ristocetin-mediated binding to platelet glycoprotein Ib
7. Structure and function of the von Willebrand factor A1 domain: Analysis with monoclonal antibodies reveals distinct binding sites involved in recognition of the platelet membrane glycoprotein Ib-IX-V complex and ristocetin-dependent activation
8. Identification of discontinuous von Willebrand factor sequences involved in complex for motion with botrocetin: A model for the regulation of von Willebrand factor binding to platelet glycoprotein Ib
9. Epitope and functional characterization of the CD42 (gpIb/IX) mAb panel
10. Requirement of leucine-rich repeats of glycoprotein (GP) Ibα for shear-dependent and static binding of von Willebrand factor to the platelet membrane GP Ib-IX-V complex
11. Mocarhagin, a novel cobra venom metalloproteinase, cleaves the platelet von Willebrand factor receptor glycoprotein Ibα: Identification of the sulfated tyrosine/anionic sequence Tyr-276 - Glu-282 of glycoprotein Ibα as a binding site for von Willebrand factor and α-thrombin
12. Antiplatelet glycoprotein Ib monoclonal antibody (OP-F1) totally abolishes ristocetin-induced von Willebrand factor binding, but has minimal effect on the botrocetin-induced binding
13. Tyrosine sulfation of the GP Ib-IX complex: Identification of sulfated residues and effect on ligand binding
14. Identification of three tyrosine residues of glycoprotein Ibα with distinct roles in von Willebrand factor and α-thrombin binding
15. Initiation of platelet adhesion by arrest onto fibrinogen or translocation on von Willebrand factor
16. Shear-dependent rolling on von Willebrand factor of mammalian cells expressing the platelet glycoprotein Ib-IX-V-complex
17. Glycoprotein (GP) Ib-IX-transfected cells roll on a von Willebrand factor matrix under flow: Importance of the GPIb/actin-binding protein (ABP-280) interaction in maintaining adhesion under high shear
18. Expression of platelet glycoprotein (GP) V in heterologous cells and evidence for its association with GP Ibα in forming a GP Ib-IX-V complex on the cell surface
19. Glycoprotein V-deficient platelets have undiminished thrombin responsiveness and do not exhibit a Bernard-Soulier phenotype
20. Increased thrombin responsiveness in platelets from mice lacking glycoprotein V
21. A mouse model of severe von Willebrand disease: Defects in hemostasis and thrombosis
22. Shear-induced platelet aggregation requires von Willebrand factor and platelet membrane glycoproteins Ib and IIb-IIIa
23. Direct demonstration of radiolabeled von Willebrand factor binding to platelet glycoprotein Ib and IIb-IIIa in the presence of shear stress
24. Characterization of the unique mechanism mediating the shear-dependent binding of soluble von Willebrand factor to platelets
25. Distinct mechanisms of platelet aggregation as a consequence of different shearing flow conditions
26. Efficient plasma membrane expression of a functional platelet glycoprotein Ib-IX complex requires the presence of its three subunits
27. Glycoprotein (GP) Ibβ is the critical subunit linking GP Ibα and GP IX in the GP Ib-IX complex: Analysis of partial complexes
28. The GP Ib-IX "complex-specific" monoclonal antibody SZ1 binds to a conformation-sensitive epitope on GP IX: Implications for the target antigen of quinine/quinidine-dependent autoantibodies
29. Ristocetin-dependent reconstitution of binding of von Willebrand factor to purified human platelet membrane glycoprotein Ib-IX complex
30. Characterization of an antiglycoprotein Ib monoclonal antibody that specifically inhibits platelet-thrombin interaction
31. Increased platelet sensitivity to ristocetin is predicted by the binding characteristics of a GPIb/IX determinant
32. A murine antiglycoprotein Ib complex monoclonal antibody, SZ 2, inhibits platelet aggregation induced by both ristocetin and collagen
33. Monoclonal antibody to human platelet glycoprotein I, part 2: Effects on human platelet function
34. Purification of the factor VIII complex
35. Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation
36. Molecular mechanisms of monocyte adhesion to interleukin-1β-stimulated endothelial cells under physiologic flow conditions
37. Necessity of conserved asparagine residues in the leucine-rich repeats of platelet glycoprotein Ibα for the proper conformation and function of the ligand-binding region
38. Von Willebrand disease: A database of point mutations, insertions and deletions: For the Consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
39. Crystal structure of the von Willebrand factor A1 domain and implications for the binding of platelet glyocoprotein Ib