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.
Similar content being viewed by others
References
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.
Church MK, Caufield JP. Mast cell and basophil function. In: Holgate ST, Church MK, editors. Allergy. London: Gower Medical Publishing, 1993:5.1–12.
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.
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.
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.
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.
Moodley I, Mongar JL, Foreman JC. Histamine release induced by dextran: the nature of the dextran receptor. Eur J Pharmacol 1982;83:69–81.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Enerbäck L, Svensson I. Isolation of rat peritoneal mast cells by centrifugation on density gradients of Percoll. J Immunol Meth 1980;39:135–45.
Nishida H, Matsui H, Nagai H. Effect of triphenyltin chloride on the release of histamine from mast cells. Arch Toxicol 1992;66:514–7.
Mackay GA, Pearce FL. A comparison of rat peritoneal mast cells purified using Percoll and Path-O-Cyte 4. Agents Actions 1992:C315–7.
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.
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.
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.
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.
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.
Inagaki N, Miura T, Nagai H, Koda A. Antiallergic mechanisms of beta-adrenergic stimulants in rats. Life Sci 1992; 51:PL201–5.
Goth A, Adams HR, Knoohuizen M. Phosphatidylserine: selective enhancer of histamine release. Science 1971;173:1034–5.
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.
Sullivan TJ, Greene WC, Parker CW. Concanavalin A-induced histamine release from normal rat mast cells. J Immunol 1975;115:278–82.
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.
Dastych J, Costa JJ, Thompson HL, Metcalfe DD. Mast cell adhesion to fibronectin. Immunol 1991;73:478–84.
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.
Yasuda M, Hasunuma Y, Adachi H, et al. Expression and function of fibronectin receptors on mast cells. Proc Jpn Soc Immunol 1992;22:346.
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.
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.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
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
Received:
Revised:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF01757359