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. 1985 Dec;56(4):667–672.

Thrombin-induced degranulation of cultured bone marrow-derived mast cells: effect on calcium uptake.

R Pervin, B I Kanner, G Marx, E Razin
PMCID: PMC1453796  PMID: 2416681

Abstract

The role of calcium in the mechanism of thrombin activation of bone marrow-derived mast cells (BMMC) was explored by measuring the changes in the uptake of 45Ca2+ into quiescent BMMC and into cells stimulated by thrombin or by IgE-antigen. The results indicate that activation of BMMC by either thrombin or IgE-antigen is Ca2+-dependent. One million BMMC, activated by 0.05-5 U thrombin, accumulated 45Ca2+ in a concentration-dependent manner, which levelled off at around 1 U thrombin. Extracellular 45Ca2+ uptake of thrombin-stimulated cells is saturable within 90 seconds and corresponds to the kinetics of histamine release, whereas that of IgE-antigen exposed cells continues unabated for over 5 min. The pattern of 45Ca2+ uptake of IgE-sensitized BMMC exposed to thrombin suggests that the pro-stimulatory locus of thrombin action on the surface membrane is distinct from that of IgE.

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Selected References

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

  1. Anton A. H., Sayre D. F. A modified fluorometric procedure for tissue histamine and its distribution in various animals. J Pharmacol Exp Ther. 1969 Apr;166(2):285–290. [PubMed] [Google Scholar]
  2. Awbrey B. J., Hoak J. C., Owen W. G. Binding of human thrombin to cultured human endothelial cells. J Biol Chem. 1979 May 25;254(10):4092–4095. [PubMed] [Google Scholar]
  3. Bar-Shavit R., Kahn A., Wilner G. D., Fenton J. W., 2nd Monocyte chemotaxis: stimulation by specific exosite region in thrombin. Science. 1983 May 13;220(4598):728–731. doi: 10.1126/science.6836310. [DOI] [PubMed] [Google Scholar]
  4. Becker E. L., Austen K. F. Mechanisms of immunologic injury of rat peritoneal mast cells. I. The effect of phosphonate inhibitors on the homocytotropic antibody-mediated histamine release and the first component of rat complement. J Exp Med. 1966 Sep 1;124(3):379–395. doi: 10.1084/jem.124.3.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Foreman J. C., Hallett M. B., Mongar J. L. The relationship between histamine secretion and 45calcium uptake by mast cells. J Physiol. 1977 Sep;271(1):193–214. doi: 10.1113/jphysiol.1977.sp011996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Holgate S. T., Lewis R. A., Austen K. F. 3',5'-Cyclic adenosine monophosphate-dependent protein kinase of the rat serosal mast cell and its immunologic activation. J Immunol. 1980 May;124(5):2093–2099. [PubMed] [Google Scholar]
  7. Ishizaka T., Hirata F., Ishizaka K., Axelrod J. Stimulation of phospholipid methylation, Ca2+ influx, and histamine release by bridging of IgE receptors on rat mast cells. Proc Natl Acad Sci U S A. 1980 Apr;77(4):1903–1906. doi: 10.1073/pnas.77.4.1903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ishizaka T., Ishizaka K., Conrad D. H., Froese A. A new concept of triggering mechanisms of IgE-mediated histamine release. Monogr Allergy. 1979;14:268–270. [PubMed] [Google Scholar]
  9. Kanno T., Cochrane D. E., Douglas W. W. Exocytosis (secretory granule extrusion) induced by injection of calcium into mast cells. Can J Physiol Pharmacol. 1973 Dec;51(12):1001–1004. doi: 10.1139/y73-153. [DOI] [PubMed] [Google Scholar]
  10. Lewis R. A., Holgate S. T., Roberts L. J., 2nd, Maguire J. F., Oates J. A., Austen K. F. Effects of indomethacin on cyclic nucleotide levels and histamine release from rat serosal mast cells. J Immunol. 1979 Oct;123(4):1663–1668. [PubMed] [Google Scholar]
  11. Metzger H. The IgE-mast cell system as a paradigm for the study of antibody mechanisms. Immunol Rev. 1978;41:186–199. doi: 10.1111/j.1600-065x.1978.tb01465.x. [DOI] [PubMed] [Google Scholar]
  12. Razin E., Ihle J. N., Seldin D., Mencia-Huerta J. M., Katz H. R., LeBlanc P. A., Hein A., Caulfield J. P., Austen K. F., Stevens R. L. Interleukin 3: A differentiation and growth factor for the mouse mast cell that contains chondroitin sulfate E proteoglycan. J Immunol. 1984 Mar;132(3):1479–1486. [PubMed] [Google Scholar]
  13. Razin E., Marx G. Thrombin-induced degranulation of cultured bone marrow-derived mast cells. J Immunol. 1984 Dec;133(6):3282–3285. [PubMed] [Google Scholar]
  14. Razin E., Mencia-Huerta J. M., Lewis R. A., Corey E. J., Austen K. F. Generation of leukotriene C4 from a subclass of mast cells differentiated in vitro from mouse bone marrow. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4665–4667. doi: 10.1073/pnas.79.15.4665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Razin E., Mencia-Huerta J. M., Stevens R. L., Lewis R. A., Liu F. T., Corey E., Austen K. F. IgE-mediated release of leukotriene C4, chondroitin sulfate E proteoglycan, beta-hexosaminidase, and histamine from cultured bone marrow-derived mouse mast cells. J Exp Med. 1983 Jan 1;157(1):189–201. doi: 10.1084/jem.157.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Razin E., Stevens R. L., Austen K. F., Caulfield J. P., Hein A., Liu F. T., Clabby M., Nabel G., Cantor H., Friedman S. Cloned mouse mast cells derived from immunized lymph node cells and from foetal liver cells exhibit characteristics of bone marrow-derived mast cells containing chondroitin sulphate E proteoglycan. Immunology. 1984 Jul;52(3):563–575. [PMC free article] [PubMed] [Google Scholar]
  17. Sullivan T. J., Parker K. L., Kulczycki A., Jr, Parker C. W. Modulation of cyclic AMP in purified rat mast cells. III. Studies on the effects of concanavalin A and anti-IgE on cyclic AMP concentrations during histamine release. J Immunol. 1976 Sep;117(3):713–716. [PubMed] [Google Scholar]
  18. Weksler B. B., Ley C. W., Jaffe E. A. Stimulation of endothelial cell prostacyclin production by thrombin, trypsin, and the ionophore A 23187. J Clin Invest. 1978 Nov;62(5):923–930. doi: 10.1172/JCI109220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. White J. R., Ishizaka T., Ishizaka K., Sha'afi R. Direct demonstration of increased intracellular concentration of free calcium as measured by quin-2 in stimulated rat peritoneal mast cell. Proc Natl Acad Sci U S A. 1984 Jul;81(13):3978–3982. doi: 10.1073/pnas.81.13.3978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. White R. P., Chapleau C. E., Dugdale M., Robertson J. T. Cerebral arterial contractions induced by human and bovine thrombin. Stroke. 1980 Jul-Aug;11(4):363–368. doi: 10.1161/01.str.11.4.363. [DOI] [PubMed] [Google Scholar]
  21. Winslow C. M., Lewis R. A., Austen K. F. Mast cell mediator release as a function of cyclic AMP-dependent protein kinase activation. J Exp Med. 1981 Oct 1;154(4):1125–1133. doi: 10.1084/jem.154.4.1125. [DOI] [PMC free article] [PubMed] [Google Scholar]

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