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Sodium fluoride evoked histamine release from mast cells. A study of cyclic AMP levels and effects of catecholamines

  • Histamine Release and Mast Cells
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Abstract

Calcium triggers the secretion of histamine from mast cells after previous exposure to sodium fluoride. The secretory process can be divided into a fluoride-activation step and a calcium-induced secretory step. It was observed that the fluoride-activation step is accompanied by an elevation of cAMP levels within the cells. The attained high levels of cAMP persist during histamine release. It was further found that catecholamines do not markedly alter the fluoride-induced histamine release. It was also confirmed that the second, but not the first, step in sodium fluoride-induced histamine secretion is inhibited by theophylline.

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References

  1. M. Kaliner andK.F. Austen,Cyclic AMP, ATP, and reversed anaphylactic histamine release from rat mast cells, J. Immun.112, 664–674 (1970).

    Google Scholar 

  2. T.J. Sullivan, K.L. Parker, S.A. Eisen andC.W. Parker,Modulation of cyclic AMP in purified rat mast cells. II. Studies of the relationship between intracellular cyclic AMP concentrations and histamine release, J. Immun.114, 1480–1485 (1975).

    PubMed  Google Scholar 

  3. T.J. Sullivan, K.L. Parker, A. Kulczycki Jr. andC.W. Parker,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. Immun.117, 713–716 (1976).

    PubMed  Google Scholar 

  4. J.C. Foreman, M.B. Hallett andJ.L. Mongar,The relationship between histamine secretion and 45 calcium uptake by mast cells, J. Physiol., Lond.271, 193–214 (1977).

    Google Scholar 

  5. J.C. Foreman, J.L. Mongar, B.D. Gomperts andL.G. Garland,A possible role for cyclic AMP in the regulation of histamine secretion and the action of cromoglycate, Biochem. Pharmac.24, 538–540 (1975).

    Article  Google Scholar 

  6. J.C. Foreman, L.G. Garland andJ.L. Mongar, The role of calcium in secretory process: model studies in mast cells. InCalcium in Biological Systems. 30th Symp. Soc. Exp. Biol., vol. 193 (EdDuncan). Cambridge University Press, Cambridge 1976.

    Google Scholar 

  7. J.A. Chabot, P.S. Riback andD.E. Cochrane,Elevated cyclic AMP levels fail to inhibit extracellular calcium-dependent histamine secretion from rat mast cells, Life Sci.28, 1155–1162 (1981).

    Article  PubMed  Google Scholar 

  8. S.A. Patkar, W. Kazimierczak andB. Diamant,Sodium fluoride — a stimulus for a calcium-triggered secretory process, Int. Archs Allergy appl. Immun.55, 193–200 (1977).

    Google Scholar 

  9. T.J. Sullivan andC.W. Parker,Pharmacologic modulation of inflammatory mediator release by rat mast cells, Am. J. Path.85, 437–463 (1976).

    PubMed  Google Scholar 

  10. P.E. Alm andG.D. Bloom,Effect of norepinephrine on in vitro histamine release from rat mast cells, Int. Archs Allergy appl. Immun.60, 60–67 (1979).

    Google Scholar 

  11. P.A. Shore, A. Burkhalter andV.H. Cohn,A method for the fluorometric assay of histamine in tissue, J. Pharmac. exp. Ther.127, 182–186 (1959).

    Google Scholar 

  12. T.J. Sullivan, K.L. Parker, W. Stenson andC.W. Parker,Modulation of cyclic AMP in purified rat mast cells. I. Responses to pharmacological, metabolic and physical stimuli, J. Immun.144, 1473–1479 (1975).

    Google Scholar 

  13. P.E. Alm andG.D. Bloom,What—if any—is the role of adrenergic mechanisms in histamine release from rat mast cells? Agents and Actions11, 60–66 (1981).

    Article  PubMed  Google Scholar 

  14. P.E. Alm andG.D. Bloom,Effects of norepinephrine on transmembrane calcium transport in rat mast cells, Int. Archs. Allergy appl. Immun.66, 427–438 (1981).

    Google Scholar 

  15. W.W. Douglas andR.D. Ueda,Mast cell secretion (histamine release) induced by 48/80: calcium-dependent exocytosis inhibited strongly by cytochalasin only when glycolysis is rate-limiting, J. Physiol., Lond.234, 97–98P (1973).

    Google Scholar 

  16. S.A. Patkar, W. Kazimierczak andB. Diamant,Histamine release by calcium from sodium fluoride-activated rat mast cells. Further evidence for a secretory process, Int. Archs Allergy appl. Immun.57, 146–154 (1978).

    Google Scholar 

  17. F.L. Pearce, M. Ennis, A. Truneh andJ.R. White,Role of Intra- and extracellular calcium in histamine release from rat peritoneal mast cells, Agents and Actions11, 51–54 (1981).

    Article  PubMed  Google Scholar 

  18. R.A. Lewis, S.T. Holgate, L.J. Roberts II, I.F. Maguire, J.A. Oates andK.F. Austen,Effects of indomethacin on cyclic nucleotide levels and histamine release from rat serosal mast cells, J. Immun.123, 1663–1668 (1979).

    PubMed  Google Scholar 

  19. B.A. Fredriksson, P.E. Alm andG.D. Bloom,Changes in mast cell plasma membrane surface structure in relation to isolation procedures and histamine secretion. In manuscript.

  20. S.J. Burwen andB.H. Satir,Plasma membrane folds on the mast cell surface and their relationship to secretory activity, J. Cell. Biol.74, 690–697 (1977).

    Article  PubMed  Google Scholar 

  21. J.C. Foreman andB.D. Gomperts,The relationship between anaphylactic histamine secretion and the permeability of the mast cell membrane to calcium, Int. Archs Allergy appl. Immun.49, 179–182 (1975).

    Google Scholar 

  22. S. Taniguchi, K. Nakazawa andM. Fujiwara,Characterization of adenylate and guanylate cyclases in rat peritoneal mast cells, Life Sci.29, 1485–1491 (1981).

    Article  PubMed  Google Scholar 

  23. D.E. Cochrane andW.W. Douglas,Calcium-induced extrusion of secretory granules (exocytosis) in mast cells exposed to 48/80 or the ionophores A23187 and X-537A, Proc. Natn. Acad. Sci. USA71, 408–412 (1974).

    Google Scholar 

  24. M. Kagayama andW.W. Douglas,Electron microscope evidence of calcium-induced exocytosis in mast cells treated with 48/80 or the ionophores A23187 and X-537A, J. Cell. Biol.62, 519–526 (1974).

    Article  PubMed  Google Scholar 

  25. D.E. Cochrane andW.W. Douglas,Histamine release by exocytosis from rat mast cells on reduction of extracellular sodium: a secretory response inhibited by calcium, strontium, barium, or magnesium, J. Physiol., Lond.257, 433–448 (1976).

    Google Scholar 

  26. M.A. Brostrom, C.H. Brostrom, B. McL. Breckenridge andD.J. Wolff,Calcium-dependent regulation of brain adenylate cyclase, Adv. Cyclic Nucleotide Res.9, 85–99 (1978).

    PubMed  Google Scholar 

  27. W.Y. Cheung, T.J. Lynch andR.W. Wallace,An endogenous Ca 2+-dependent activator protein of brain adenylate cyclase and cyclic nucleotide phosphodiesterase, Adv. Cyclic Nucleotide Res.9, 232–251 (1978).

    Google Scholar 

  28. M. Ennis, A. Truneh, J.R. White andF.L. Pearce,Inhibition of histamine secretion from mast cells, Nature289, 186–187 (1981).

    Article  PubMed  Google Scholar 

  29. P.E. Alm andG.D. Bloom,Cyclic nucleotide involvement in histamine release from mast cells — a re-evaluation, Life Sci.30, 213–218 (1982).

    Article  PubMed  Google Scholar 

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Alm, P.E. Sodium fluoride evoked histamine release from mast cells. A study of cyclic AMP levels and effects of catecholamines. Agents and Actions 13, 132–137 (1983). https://doi.org/10.1007/BF01967316

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