Thrombotic thrombocytopenia induced in dogs and pigs. The role of plasma and platelet vWF in animal models of thrombotic thrombocytopenic purpura.

Thrombotic thrombocytopenia with severe depletion of plasma von Willebrand factor (vWF) was induced in normal large animals (5 dogs and 2 pigs) by botrocetin, a Bothrops factor requiring vWF for platelet agglutination. Botrocetin (90 to 100 U/kg, 2.14 to 2.38 mg/kg, in a single i.v. injection) reduced plasma vWF activity to < 0.1 U/mL for 24 hours. During this period, multimeric analysis of plasma vWF antigen (Ag) revealed the loss of intermediate- and high-molecular-weight forms with a concomitant increase in lower molecular weight forms. A moderate reduction in factor VIII (FVIII) activity was observed. The vWF reduction was accompanied by transient thrombocytopenia and prolonged bleeding times during the deficiency state. Occlusive platelet thrombi were detected by transmission electron microscopy in the microcirculation of lung and spleen but not kidney or brain 30 minutes after the botrocetin injection. Recovery of plasma vWF and platelet count occurred within 48 hours and was associated with the appearance in the plasma of unusually large forms of vWF:Ag multimers. The vWF:Ag multimer distribution was normal at 72 hours. The ultrastructural distribution of vWF in unstimulated normal porcine and canine platelets was examined by using immunogold staining. VWF was detected in the alpha-granules of normal pig platelets but was not observed in platelets from normal dogs. However, both animals developed thrombotic thrombocytopenia when injected with botrocetin. A second group of animals (2 dogs and 3 pigs) with von Willebrand disease (vWD) was given a single botrocetin injection (90 to 100 U/kg). No thrombocytopenia occurred.(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  D. Bellinger,et al.  Preservation of hemostatic and structural properties of rehydrated lyophilized platelets: potential for long-term storage of dried platelets for transfusion. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. Meyer,et al.  von Willebrand Factor: Structure and Function , 1993, Thrombosis and Haemostasis.

[3]  D. Bellinger,et al.  The roles of von Willebrand factor and factor VIII in arterial thrombosis: studies in canine von Willebrand disease and hemophilia A , 1993 .

[4]  Pille Harrison,et al.  Porcine platelets contain an increased quantity of ultra‐high molecular weight von Willebrand factor and numerous alpha‐granular tubular structures , 1993, British journal of haematology.

[5]  C. Ward,et al.  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. , 1992, Biochemistry.

[6]  J. Moake,et al.  Hemolytic uremic syndrome and thrombotic thrombocytopenic purpura , 1992 .

[7]  H. Mohri,et al.  Identification of discontinuous von Willebrand factor sequences involved in complex formation with botrocetin. A model for the regulation of von Willebrand factor binding to platelet glycoprotein Ib. , 1991, The Journal of biological chemistry.

[8]  J. Scott,et al.  Dimeric ristocetin flocculates proteins, binds to platelets, and mediates von Willebrand factor-dependent agglutination of platelets. , 1991, The Journal of biological chemistry.

[9]  Read Ms,et al.  Glycoprotein Ib bioassays. Activity levels in Bernard-Soulier syndrome and in stored blood bank platelets. , 1991 .

[10]  F. Siddiqui,et al.  Platelet Agglutinating Protein p37 Causes Platelet Agglutination through its Binding to Membrane Glycoprotein IV , 1991, Thrombosis and Haemostasis.

[11]  F. Siddiqui,et al.  Binding of Platelet Agglutinating Protein p 37 from the Plasma of a Patient with Thrombotic Thrombocytopenic Purpura to Human Platelets , 1991, Thrombosis and Haemostasis.

[12]  R. Cartun,et al.  A Simplified Technique for the Ultrastructural Localization of Cytoskeletal Filament Proteins By Immunogold Electron Microscopy , 1990 .

[13]  J. Moake Recent observations on the pathophysiology of thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. , 1990, Hematologic pathology.

[14]  J. Moake,et al.  Abnormalities of von Willebrand factor multimers in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. , 1989, The American journal of medicine.

[15]  M. Read,et al.  Role of botrocetin in platelet agglutination: formation of an activated complex of botrocetin and von Willebrand factor , 1989 .

[16]  R. Reddick,et al.  Thrombotic thrombocytopenia with von Willebrand factor deficiency induced by botrocetin. An animal model. , 1988, Laboratory investigation; a journal of technical methods and pathology.

[17]  J. Moake,et al.  Shear-induced platelet aggregation can be mediated by vWF released from platelets, as well as by exogenous large or unusually large vWF multimers, requires adenosine diphosphate, and is resistant to aspirin , 1988 .

[18]  J. Kelton,et al.  Relationship between platelet aggregating factor and von Willebrand factor in thrombotic thrombocytopenic purpura , 1987, British journal of haematology.

[19]  E. Lian Pathogenesis of thrombotic thrombocytopenic purpura. , 1987, Seminars in hematology.

[20]  J. Moake,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. , 1986, The Journal of clinical investigation.

[21]  L. Drouet,et al.  Absence of tubular structures and immunolabeling for von Willebrand factor in the platelet alpha-granules from porcine von Willebrand disease. , 1986, Blood.

[22]  R. D. Wade,et al.  Amino acid sequence of human von Willebrand factor. , 1986, Biochemistry.

[23]  R. Wagner,et al.  Visualization of von Willebrand Factor Multimers by Immunoenzymatic Stain Using Avidin-Biotin Peroxidase Complex , 1986, Thrombosis and Haemostasis.

[24]  J. Moake,et al.  Case Report: Von Willebrand Factor Abnormalities and Endothelial Cell Perturbation in a Patient with Acute Thrombotic Thrombocytopenic Purpura , 1986 .

[25]  J. Moake,et al.  Thrombotic thrombocytopenic purpura and the haemolytic-uraemic syndrome: evolving concepts of pathogenesis and therapy. , 1986, Clinics in haematology.

[26]  M. Read,et al.  Determinants of von Willebrand factor activity elicited by ristocetin and botrocetin: studies on a human von Willebrand factor-binding antibody. , 1985, Seminars in thrombosis and hemostasis.

[27]  D. Meyer,et al.  Eccentric localization of von Willebrand factor in an internal structure of platelet alpha-granule resembling that of Weibel-Palade bodies. , 1985, Blood.

[28]  J. Kelton,et al.  The detection of a platelet-agglutinating factor in thrombotic thrombocytopenic purpura. , 1984, Annals of internal medicine.

[29]  M. Weinstein,et al.  Abnormal VIII: von Willebrand factor patterns in the plasma of patients with the hemolytic-uremic syndrome , 1984 .

[30]  D. Deykin,et al.  Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. , 1982, The New England journal of medicine.

[31]  R. Reddick,et al.  Platelet adhesion to damaged coronary arteries: Comparison in normal and von Willebrand disease swine. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Z. Ruggeri,et al.  The complex multimeric composition of factor VIII/von Willebrand factor , 1981 .

[33]  M. Read,et al.  Von Willebrand syndrome induced by a Bothrops venom factor: bioassay for venom coagglutinin. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[34]  H. Reisner,et al.  The multimeric distribution of factor VIII-related antigen studied by an improved crossed-immunoelectrophoresis technique. , 1981, The Journal of laboratory and clinical medicine.

[35]  M. Read,et al.  Use of venom coagglutinin and lyophilized platelets in testing for platelet-aggregating von Willebrand factor. , 1980, Blood.

[36]  M. Kennedy,et al.  PLATELET AGGREGATING FACTOR IN THROMBOCYTOPENIC PURPURA , 1979, The Lancet.

[37]  P. Blatt,et al.  Thrombotic thrombocytopenic purpura: a pathology review. , 1979, JAMA.

[38]  J. Byrnes,et al.  Presence of a platelet aggregating factor in the plasma of patients with thrombotic thrombocytopenic purpura (TTP) and its inhibition by normal plasma. , 1979, Blood.

[39]  K M Brinkhous,et al.  Preservation of platelet receptors for platelet aggregating factor/von Willebrand factor by air drying, freezing, or lyophilization: new stable platelet preparations for von Willebrand factor assays. , 1978, Thrombosis research.

[40]  M. Read,et al.  Venom coagglutinin: an activator of platelet aggregation dependent on von Willebrand factor. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[41]  E. Moschcowitz,et al.  AN ACUTE FEBRILE PLEIOCHROMIC ANEMIA WITH HYALINE THROMBOSIS OF THE TERMINAL ARTERIOLES AND CAPILLARIES: AN UNDESCRIBED DISEASE , 1925 .

[42]  C. Laurell,et al.  Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies. , 1966, Analytical biochemistry.

[43]  E. Gangarosa,et al.  Ristocetin-induced thrombocytopenia: site and mechanism of action. , 1960, Archives of internal medicine.

[44]  K. Brinkhous,et al.  Effect of antihemophilic factor on one-stage clotting tests; a presumptive test for hemophilia and a simple one-stage antihemophilic factor assy procedure. , 1953, The Journal of laboratory and clinical medicine.

[45]  E. Mertz THE ANOMALY OF A NORMAL DUKE'S AND A VERY PROLONGED SALINE BLEEDING TIME IN SWINE SUFFERING FROM AN INHERITED BLEEDING DISEASE , 1942 .