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. 1985 Nov 15;232(1):305–308. doi: 10.1042/bj2320305

Mechanisms of thrombin-induced modifications of human platelet cytoskeleton.

F Sinigaglia, C L Balduini, A Bisio, C Balduini
PMCID: PMC1152877  PMID: 4084237

Abstract

Thrombin treated with phenylmethanesulphonyl fluoride, like active enzyme, promotes modifications to human platelet cytoskeleton. The removal of active thrombin by hirudin partially reverses this process. Chymotrypsin-treated platelets do not modify their cytoskeleton after thrombin stimulus, but are still able to increase their adhesiveness to collagen. It is concluded that thrombin influences the cytoskeleton and adhesion by non-enzymic mechanisms which may be mediated by different modulators.

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Selected References

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  1. Balduini C. L., Sinigaglia F., Salvini P., Balduini C. The role of plasma fibronectin in platelet adhesion to collagen. Haemostasis. 1984;14(2):158–163. doi: 10.1159/000215051. [DOI] [PubMed] [Google Scholar]
  2. Berndt M. C., Phillips D. R. Purification and preliminary physicochemical characterization of human platelet membrane glycoprotein V. J Biol Chem. 1981 Jan 10;256(1):59–65. [PubMed] [Google Scholar]
  3. Brass L. F., Faile D., Bensusan H. B. Direct measurement of the platelet:collagen interaction by affinity chromatography on collagen/Sepharose. J Lab Clin Med. 1976 Mar;87(3):525–534. [PubMed] [Google Scholar]
  4. Casella J. F., Masiello N. C., Lin S., Bell W., Zucker M. B. Identification of fibrinogen derivatives in the Triton-insoluble residue of human blood platelets. Cell Motil. 1983;3(1):21–30. doi: 10.1002/cm.970030103. [DOI] [PubMed] [Google Scholar]
  5. Collen D., Lijnen H. R., De Cock F., Durieux J. P., Loffet A. Kinetic properties of tripeptide lysyl chloromethyl ketone and lysyl p-nitroanilide derivatives towards trypsin-like serine proteinases. Biochim Biophys Acta. 1980 Sep 9;615(1):158–166. doi: 10.1016/0005-2744(80)90019-4. [DOI] [PubMed] [Google Scholar]
  6. Fox J. E., Goll D. E., Reynolds C. C., Phillips D. R. Identification of two proteins (actin-binding protein and P235) that are hydrolyzed by endogenous Ca2+-dependent protease during platelet aggregation. J Biol Chem. 1985 Jan 25;260(2):1060–1066. [PubMed] [Google Scholar]
  7. Ganguly P., Gould N. L. Thrombin receptors of human platelets: thrombin binding and antithrombin properties of glycoprotein I. Br J Haematol. 1979 May;42(1):137–145. doi: 10.1111/j.1365-2141.1979.tb03706.x. [DOI] [PubMed] [Google Scholar]
  8. Holmsen H., Dangelmaier C. A., Rongved S. Tight coupling of thrombin-induced acid hydrolase secretion and phosphatidate synthesis to receptor occupancy in human platelets. Biochem J. 1984 Aug 15;222(1):157–167. doi: 10.1042/bj2220157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kreuzer K. N. Recognition of single-stranded DNA by the bacteriophage T4-induced type II topoisomerase. J Biol Chem. 1984 Apr 25;259(8):5347–5354. [PubMed] [Google Scholar]
  10. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  11. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  12. Lundblad R. L. A rapid method for the purification of bovine thrombin and the inhibition of the purified enzyme wtih phenylmethylsulfonyl fluoride. Biochemistry. 1971 Jun 22;10(13):2501–2506. doi: 10.1021/bi00789a012. [DOI] [PubMed] [Google Scholar]
  13. Martin B. M., Feinman R. D., Detwiler T. C. Platelet stimulation by thrombin and other proteases. Biochemistry. 1975 Mar 25;14(6):1308–1314. doi: 10.1021/bi00677a032. [DOI] [PubMed] [Google Scholar]
  14. Okumura T., Hasitz M., Jamieson G. A. Platelet glycocalicin. Interaction with thrombin and role as thrombin receptor of the platelet surface. J Biol Chem. 1978 May 25;253(10):3435–3443. [PubMed] [Google Scholar]
  15. Okumura T., Jamieson G. A. Platelet glycocalicin. I. Orientation of glycoproteins of the human platelet surface. J Biol Chem. 1976 Oct 10;251(19):5944–5949. [PubMed] [Google Scholar]
  16. Phillips D. R., Jennings L. K., Edwards H. H. Identification of membrane proteins mediating the interaction of human platelets. J Cell Biol. 1980 Jul;86(1):77–86. doi: 10.1083/jcb.86.1.77. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Rotman A. Receptor and non receptor-mediated activation of blood platelets. Effect on membrane-cytoskeleton interaction. Biochem Biophys Res Commun. 1984 May 16;120(3):898–906. doi: 10.1016/s0006-291x(84)80192-8. [DOI] [PubMed] [Google Scholar]
  18. Sinigaglia F., Balduini C. L., Bisio A., Balduini C. Thrombin increases the adhesion of washed human platelets to collagen. Br J Haematol. 1985 Apr;59(4):587–592. doi: 10.1111/j.1365-2141.1985.tb07352.x. [DOI] [PubMed] [Google Scholar]
  19. Tam S. W., Fenton J. W., 2nd, Detwiler T. C. Dissociation of thrombin from platelets by hirudin. Evidence for receptor processing. J Biol Chem. 1979 Sep 25;254(18):8723–8725. [PubMed] [Google Scholar]
  20. Tam S. W., Fenton J. W., 2nd, Detwiler T. C. Platelet thrombin receptors. Binding of alpha-thrombin is coupled to signal generation by a chymotrypsin-sensitive mechanism. J Biol Chem. 1980 Jul 25;255(14):6626–6632. [PubMed] [Google Scholar]
  21. Tollefsen D. M., Feagler J. R., Majerus P. W. The binding of thrombin to the surface of human platelets. J Biol Chem. 1974 Apr 25;249(8):2646–2651. [PubMed] [Google Scholar]
  22. Tsujinaka T., Sakon M., Kambayashi J., Kosaki G. Cleavage of cytoskeletal proteins by two forms of Ca2+ activated neutral proteases in human platelets. Thromb Res. 1982 Oct 15;28(2):149–156. doi: 10.1016/0049-3848(82)90257-2. [DOI] [PubMed] [Google Scholar]
  23. Wang C., Smith R. L. Lowry determination of protein in the presence of Triton X-100. Anal Biochem. 1975 Feb;63(2):414–417. doi: 10.1016/0003-2697(75)90363-2. [DOI] [PubMed] [Google Scholar]
  24. Zavoico G. B., Feinstein M. B. Cytoplasmic Ca2+ in platelets is controlled by cyclic AMP: antagonism between stimulators and inhibitors of adenylate cyclase. Biochem Biophys Res Commun. 1984 Apr 30;120(2):579–585. doi: 10.1016/0006-291x(84)91294-4. [DOI] [PubMed] [Google Scholar]

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