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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1982 Dec;79(23):7297–7301. doi: 10.1073/pnas.79.23.7297

Transient kinetics of the rapid shape change of unstirred human blood platelets stimulated with ADP.

D A Deranleau, D Dubler, C Rothen, E F Lüscher
PMCID: PMC347326  PMID: 6961409

Abstract

Unstirred (isotropic) suspensions of human blood platelets stimulated with ADP in a stopped-flow laser turbidimeter exhibit a distinct extinction maximum during the course of the classical rapid conversion of initially smooth flat discoid cells to smaller-body spiny spheres. This implies the existence of a transient intermediate having a larger average light scattering cross section (extinction coefficient) than either the disc or the spiny sphere. Monophasic extinction increases reaching the same final value were observed when either discoid or spiny sphere platelets were converted to smooth spheres by treatment with chlorpromazine, and sphering of discoid cells was accompanied by a larger total extinction change than the retraction of pseudopods by already spherical cells. These and other results suggest that the ADP-induced transient state represents platelets that are approximately as "spherical" as the irregular spiny sphere but lack the characteristic long pseudopods and as a consequence are larger bodied. Fitting the ADP progress curves to the series reaction A leads to B leads to C by means of the light scattering equivalent of the Beer-Lambert law yielded scattering cross sections that are consistent with this explanation. The rate constants for the two reaction steps were identical, indicating that ADP activation corresponds to a continuous random (Poisson) process with successive apparent states "disc," "sphere," and "spiny sphere," whose individual probabilities are determined by a single rate-limiting step.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BORN G. V., CROSS M. J. THE AGGREGATION OF BLOOD PLATELETS. J Physiol. 1963 Aug;168:178–195. doi: 10.1113/jphysiol.1963.sp007185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Born G. V., Dearnley R., Foulks J. G., Sharp D. E. Quantification of the morphological reaction of platelets to aggregating agents and of its reversal by aggregation inhibitors. J Physiol. 1978 Jul;280:193–212. doi: 10.1113/jphysiol.1978.sp012380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Born G. V. Observations on the change in shape of blood platelets brought about by adenosine diphosphate. J Physiol. 1970 Aug;209(2):487–511. doi: 10.1113/jphysiol.1970.sp009176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Deranleau D. A., Dubler D. Time-dependent total extinction analysis for simple reactions involving intermediates. Anal Biochem. 1981 Jul 1;114(2):411–414. doi: 10.1016/0003-2697(81)90503-0. [DOI] [PubMed] [Google Scholar]
  5. Deranleau D. A., Rothen C., Streit M., Dubler D., Lüscher E. F. A stopped-flow laser turbidimeter for studying changes in the shape of cells stimulated by external agents. Anal Biochem. 1980 Mar 1;102(2):288–290. doi: 10.1016/0003-2697(80)90154-2. [DOI] [PubMed] [Google Scholar]
  6. Frojmovic M. M., Panjwani R. Geometry of normal mammalian platelets by quantitative microscopic studies. Biophys J. 1976 Sep;16(9):1071–1089. doi: 10.1016/S0006-3495(76)85756-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Graf M., Richards J. G., Colombo V., Pletscher A. Shape change reaction of platelets in protein-free medium: ultramorphology. Experientia. 1979 Jun 15;35(6):840–842. doi: 10.1007/BF01968285. [DOI] [PubMed] [Google Scholar]
  8. Latimer P., Born G. V., Michal F. Application of light-scattering theory to the optical effects associated with the morphology of blood platelets. Arch Biochem Biophys. 1977 Apr 15;180(1):151–159. doi: 10.1016/0003-9861(77)90019-4. [DOI] [PubMed] [Google Scholar]
  9. Latimer P. Light scattering vs. microscopy for measuring average cell size and shape. Biophys J. 1979 Jul;27(1):117–126. doi: 10.1016/S0006-3495(79)85206-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Latimer P., Moore D. M., Bryant F. D. Changes in total light scattering and absorption caused by changes in particle conformation. J Theor Biol. 1968 Dec;21(3):348–367. doi: 10.1016/0022-5193(68)90120-3. [DOI] [PubMed] [Google Scholar]
  11. Laufer N., Grover N. B., Ben-Sasson S., Freund H. Effects of adenosine diphosphate, colchicine and temperature on size of human platelets. Thromb Haemost. 1979 May 25;41(3):491–497. [PubMed] [Google Scholar]
  12. Massini P., Lüscher E. F. The induction of the release reaction in human blood platelets by close cell contact. Thromb Diath Haemorrh. 1971;25(1):13–20. [PubMed] [Google Scholar]
  13. Milton J. G., Frojmovic M. M. Shape-changing agents produce abnormally large platelets in a hereditary "giant platelets syndrome (MPS)". J Lab Clin Med. 1979 Jan;93(1):154–161. [PubMed] [Google Scholar]
  14. O'brien J. R. Platelet aggregation: Part I Some effects of the adenosine phosphates, thrombin, and cocaine upon platelet adhesiveness. J Clin Pathol. 1962 Sep;15(5):446–452. doi: 10.1136/jcp.15.5.446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. White J. G. Effects of ethylenediamine tetracetic acid (EDTA) on platelet structure. Scand J Haematol. 1968;5(4):241–254. doi: 10.1111/j.1600-0609.1968.tb01743.x. [DOI] [PubMed] [Google Scholar]
  16. White J. G. Fine structural alterations induced in platelets by adenosine diphosphate. Blood. 1968 May;31(5):604–622. [PubMed] [Google Scholar]

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