Skip to main content
Immunology logoLink to Immunology
. 1982 Jun;46(2):353–359.

Characteristics of histamine secretion from rat peritoneal mast cells sensitized to the nematode Nippostrongylus brasiliensis.

J R White, F L Pearce
PMCID: PMC1555375  PMID: 6177624

Abstract

Peritoneal mast cells from rats immunized with the nematode Nippostrongylus brasiliensis released histamine on challenge with antigen in both the presence and absence of added calcium. The response under the latter conditions was abolished by depletion of sequestered stores of the cation and probably reflected mobilization of these stores. The release was potentiated by brief pretreatment with chelating agents and inhibited (in the absence of phosphatidyl serine, PS) by supramaximal concentrations of calcium. Calcium bound to superficial sites in the membrane may then regulate the secretory process. Histamine release in both the presence and absence of calcium was enhanced by adenosine. Only the former response was potentiated by PS, in keeping with the view that the lipid promotes influx of the cation from the extracellular environment. The activated state induced by antigen decayed with time but PS slowed this process. Histamine secretion in the absence of calcium was more rapid than in the presence of the cation, consistent with the release of bound calcium in a pulse of short duration.

Full text

PDF
353

Selected References

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

  1. Atkinson G., Ennis M., Pearce F. L. The effect of alkaline earth cations on the release of histamine from rat peritoneal mast cells treated with compound 48/80 and peptide 401. Br J Pharmacol. 1979 Mar;65(3):395–402. doi: 10.1111/j.1476-5381.1979.tb07843.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ennis M., Truneh A., White J. R., Pearce F. L. Calcium pools involved in histamine release from rat mast cells. Int Arch Allergy Appl Immunol. 1980;62(4):467–471. doi: 10.1159/000232551. [DOI] [PubMed] [Google Scholar]
  3. Foreman J. C., Mongar J. L. The role of the alkaline earth ions in anaphylactic histamine secretion. J Physiol. 1972 Aug;224(3):753–769. doi: 10.1113/jphysiol.1972.sp009921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kazimierczak W., Diamant B. Mechanisms of histamine release in anaphylactic and anaphylactoid reactions. Prog Allergy. 1978;24:295–365. [PubMed] [Google Scholar]
  5. Keller R. Immune reactions to Nippostrongylus brasiliensis in the rat. I. Characteristics of primary and secondary immune response in vivo. Int Arch Allergy Appl Immunol. 1970;37(2):197–215. doi: 10.1159/000230233. [DOI] [PubMed] [Google Scholar]
  6. Marquardt D. L., Parker C. W., Sullivan T. J. Potentiation of mast cell mediator release by adenosine. J Immunol. 1978 Mar;120(3):871–878. [PubMed] [Google Scholar]
  7. Ogilvie B. M. Reagin-like antibodies in rats infected with the nematode parasite Nippostrongylus brasiliensis. Immunology. 1967 Feb;12(2):113–131. [PMC free article] [PubMed] [Google Scholar]
  8. SHORE P. A., BURKHALTER A., COHN V. H., Jr A method for the fluorometric assay of histamine in tissues. J Pharmacol Exp Ther. 1959 Nov;127:182–186. [PubMed] [Google Scholar]
  9. Truneh A., Pearce F. L. Characteristics of and calcium requirements for histamine release from rat peritoneal mast cells treated with concanavalin A. Int Arch Allergy Appl Immunol. 1981;66(1):68–75. doi: 10.1159/000232801. [DOI] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES