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Characterization of purification-associated reduction in IgE-dependent histamine release from rat peritoneal mast cells

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Abstract

Histamine release from purified rat peritoneal mast cells (PMC) was examined and compared to that from a non-purified preparation (PEC). Both PEC and PMC released similar amounts of histamine upon stimulation with compound 48/80, calcium ionophore A23187 and substance P. In contrast, IgE-dependent histamine release from PMC caused by antigen, anti-IgE and concanavalin A was very low compared to that of PEC. The reduced IgE-dependent histamine release from PMC, however, was recovered when PMC was reconstituted with non-mast cells (NMC) present in the peritoneal cavity. The effect was time-dependent and reached a plateau in 30 min. NMC from both sensitized and non-sensitized rats recovered the reduced histamine release from PMC dose-dependently. The potentiating effect of NMC was observed even in the presence of excess amount of phosphatidylserine. Supernatants of NMC and a mixture of PMC and NMC incubated for 1 hr at 37°C, however, failed to potentiate the histamine release. These results demonstrate that IgE-dependent histamine release from rat peritoneal mast cells is upregulated by other cells present in the peritoneal cavity, and that the mechanism involved is distinct from that of phosphatidylserine.

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References

  1. Ishizaka K, Ishizaka T. Immunology of IgE-mediated hypersensitivity. In: Middleton E Jr, Reed CE, Ellis EF, editors. Allergy, principles and practice. St. Louis: CV Mosby Company, 1983:43–73.

    Google Scholar 

  2. Church MK, Caufield JP. Mast cell and basophil function. In: Holgate ST, Church MK, editors. Allergy. London: Gower Medical Publishing, 1993:5.1–12.

    Google Scholar 

  3. Brostoff J, Hall T. Hypersensitivity-type I. In: Roitt I, Brostoff J, Male D, editors. Immunology. London: Mosby-Year Book Europe, 1993:19.1–22.

    Google Scholar 

  4. White MV. Mast cell secretagogues. In: Kaliner MA, Metcalfe DD, editors. The mast cell in health and disease. New York: Marcel Dekker, 1993:109–28.

    Google Scholar 

  5. Cochrane DE, Douglas WW. Calcium-induced extrusion of secretory granules (exocytosis) in mast cells exposed to 48/80 or the ionophore A-23187 and X-537A. Proc Natl Acad Sci USA 1974;71:408–12.

    PubMed  Google Scholar 

  6. Fewtrell CMS, Forman JC, Jordan CC, Oehme P, Renner H, Stewart JM. The effects of substance P on histamine and 5-hydroxytryptamine release in the rat. J Physiol 1983;320:393–411.

    Google Scholar 

  7. Moodley I, Mongar JL, Foreman JC. Histamine release induced by dextran: the nature of the dextran receptor. Eur J Pharmacol 1982;83:69–81.

    PubMed  Google Scholar 

  8. Shanahan F, Lee TDG, Bienenstock J, Befus AD. The influence of endorphins on peritoneal and mucosal mast cell secretion. J All Clin Immunol 1984;74:499–504.

    Google Scholar 

  9. Koibuchi Y, Ichikawa A, Nakagawa N, Tomita K. Histamine release induced from mast cells by active components of compound 48/80. Eur J Pharmacol 1985;115:163–70.

    PubMed  Google Scholar 

  10. Nakajima K, Hirai K, Yamaguchi K, et al. Stem cell factor has histamine releasing activity in rat connective tissue-type mast cells. Biochim Biophys Res Commun 1992;183:1078–83.

    Google Scholar 

  11. Bischoff SC, Dahinden CA.c-Kit ligand: a unique potentiator of mediator release by human lung mast cells. J Exp Med 1993;175:237–44.

    Google Scholar 

  12. Sullivan TJ, Parker KL, Kulczycki A Jr, Parker CW. 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;117:713–6.

    PubMed  Google Scholar 

  13. Wells E, Mann J. Phosphorylation of a mast cell protein in response to treatment with anti-allergic compounds. Implications for the mode of action of sodium cromoglycate. Biochem Pharmacol 1983;32:837–42.

    PubMed  Google Scholar 

  14. Swieter M, Ghali WA, Rimmer C, Befus D. Interferon-α/β inhibits IgE-dependent histamine release from rat mast cells. Immunol 1989;66:606–10.

    Google Scholar 

  15. Saito H, Ishizaka K, Ishizaka T. Effect of nonhydrolyzable guanosine phosphate on IgE-mediated activation of phospholipase C and histamine release from rodent mast cells. J Immunol 1989;143:250–8.

    PubMed  Google Scholar 

  16. Sullivan TJ, Parker KL, Stenson W, Parker CW. Modulation of cyclic AMP in purified rat mast cells. I. Responses to pharmacologic, metabolic, and physical stimuli. J Immunol 1975;114:1473–9.

    PubMed  Google Scholar 

  17. Enerbäck L, Svensson I. Isolation of rat peritoneal mast cells by centrifugation on density gradients of Percoll. J Immunol Meth 1980;39:135–45.

    Google Scholar 

  18. Nishida H, Matsui H, Nagai H. Effect of triphenyltin chloride on the release of histamine from mast cells. Arch Toxicol 1992;66:514–7.

    PubMed  Google Scholar 

  19. Mackay GA, Pearce FL. A comparison of rat peritoneal mast cells purified using Percoll and Path-O-Cyte 4. Agents Actions 1992:C315–7.

  20. Kohno S, Nakao S, Ogawa K, Yamamura H, Nabe T, Ohata K. Possible participation of histamine H3-receptors in the regulation of anaphylactic histamine release from isolated rat peritoneal mast cells. Japan J Pharmacol 1994;66:173–80.

    Google Scholar 

  21. Inagaki N, Kawasaki H, Ueno M, Nagai H, Koda A. Potentiation of antigen-induced histamine release from rat peritoneal mast cells through a direct interaction between mast cells and non-mast cells. Life Sci 1994;54:1403–9.

    PubMed  Google Scholar 

  22. Eisen HN, Belman S, Carsten ME. The reaction of 2,4-dinitrobenzenesulfonic acid with free amino groups of proteins. J Am Chem Soc 1953;75:4583–5.

    Google Scholar 

  23. May CD, Lyman M, Alberto R, Cheng J. Procedures for immunochemical study of histamine release from leukocytes with small volume of blood. J All 1970;46:12–20.

    Google Scholar 

  24. Yamatodani A, Fukuda H, Wada H, Iwaeda T, Watanabe T. High-performance liquid chromatographic determination of plasma and brain histamine without previous purification of biological samples; cation-exchange chromatography coupled with post-column derivatization fluorometry. J Chromatogr 1985;344:115–23.

    PubMed  Google Scholar 

  25. Inagaki N, Miura T, Nagai H, Koda A. Antiallergic mechanisms of beta-adrenergic stimulants in rats. Life Sci 1992; 51:PL201–5.

    PubMed  Google Scholar 

  26. Goth A, Adams HR, Knoohuizen M. Phosphatidylserine: selective enhancer of histamine release. Science 1971;173:1034–5.

    PubMed  Google Scholar 

  27. Grosman N, Diamant B. The influence of phosphatidyl serine on the release of histamine from isolated rat mast cells induced by different agents. Agents Actions 1975;5:296–301.

    PubMed  Google Scholar 

  28. Sullivan TJ, Greene WC, Parker CW. Concanavalin A-induced histamine release from normal rat mast cells. J Immunol 1975;115:278–82.

    PubMed  Google Scholar 

  29. Thompson HL, Burbelo PD, Yamada Y, Kleinman HK, Metcalfe DD. Mast cells chemotax to laminin with enhancement after IgE-mediated activation. J Immunol 1989;143:4188–92.

    PubMed  Google Scholar 

  30. Dastych J, Costa JJ, Thompson HL, Metcalfe DD. Mast cell adhesion to fibronectin. Immunol 1991;73:478–84.

    Google Scholar 

  31. Thompson HL, Thomas L, Metcalfe DD. Murine mast cells attach to and migrate on laminin-, fibronectin-, and matrigelcoated surfaces in response to Fc∈RI-mediated signals. Clin Exp All 1993;23:270–5.

    Google Scholar 

  32. Yasuda M, Hasunuma Y, Adachi H, et al. Expression and function of fibronectin receptors on mast cells. Proc Jpn Soc Immunol 1992;22:346.

    Google Scholar 

  33. Ra C, Yasuda M, Yagita H, Okumura K. Fibronectin receptor integrins are involved in mast cell activation. J All Clin Immunol 1994;94:625–8.

    Google Scholar 

  34. Yasuda M, Hasunuma Y, Adachi H, et al. Expression and function of fibronectin binding integrins on rat mast cells. Int Immunol 1995;7:251–8.

    PubMed  Google Scholar 

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Inagaki, N., Kawasaki, H. & Nagai, H. Characterization of purification-associated reduction in IgE-dependent histamine release from rat peritoneal mast cells. Inflamm Res 44, 541–547 (1995). https://doi.org/10.1007/BF01757359

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