Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1987 Oct 1;247(1):95–99. doi: 10.1042/bj2470095

A major role for phospholipase A2 in antigen-induced arachidonic acid release in rat mast cells.

K Yamada 1, Y Okano 1, K Miura 1, Y Nozawa 1
PMCID: PMC1148374  PMID: 3120703

Abstract

Cross-linking of IgE receptors by antigen stimulation leads to histamine release and arachidonic acid release in rat peritoneal mast cells. Investigators have reported a diverse distribution of [3H]arachidonate that is dependent on labelling conditions. Mast cells from rat peritoneal cavity were labelled with [3H]arachidonic acid for different periods of time at either 30 or 37 degrees C. Optimum labelling was found to be after 4 h incubation with [3H]arachidonate at 30 degrees C, as judged by cell viability (Trypan Blue uptake), responsiveness (histamine release) and distribution of radioactivity. Alterations in 3H-radioactivity distribution in mast cells labelled to equilibrium were examined on stimulation with antigen (2,4-dinitrophenyl-conjugated Ascaris suum extract). The results indicated that [3H]arachidonic acid was lost mainly from phosphatidylcholine and, to a lesser extent, from phosphatidylinositol. A transient appearance of radiolabelled phosphatidic acid and diacylglycerol indicated phosphatidylinositol hydrolysis by phospholipase C. Pretreatment with a phospholipase A2 inhibitor, mepacrine, substantially prevented the antigen-induced liberation of [3H]arachidonic acid from phosphatidylcholine. It can be thus concluded that, in the release of arachidonic acid by antigen-stimulated mast cells, the phospholipase A2 pathway, in which phosphatidylcholine is hydrolysed, serves as the major one, the phospholipase C/diacylglycerol lipase pathway playing only a minor role.

Full text

PDF
95

Selected References

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

  1. BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
  2. Benjamin C. W., Tarpley W. G., Gorman R. R. Loss of platelet-derived growth factor-stimulated phospholipase activity in NIH-3T3 cells expressing the EJ-ras oncogene. Proc Natl Acad Sci U S A. 1987 Jan;84(2):546–550. doi: 10.1073/pnas.84.2.546. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Besterman J. M., Duronio V., Cuatrecasas P. Rapid formation of diacylglycerol from phosphatidylcholine: a pathway for generation of a second messenger. Proc Natl Acad Sci U S A. 1986 Sep;83(18):6785–6789. doi: 10.1073/pnas.83.18.6785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Colard O., Breton M., Bereziat G. Arachidonate mobilization in diacyl, alkylacyl and alkenylacyl phospholipids on stimulation of rat platelets by thrombin and the Ca2+ ionophore A23187. Biochem J. 1986 Feb 1;233(3):691–695. doi: 10.1042/bj2330691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Daniel L. W., Waite M., Wykle R. L. A novel mechanism of diglyceride formation. 12-O-tetradecanoylphorbol-13-acetate stimulates the cyclic breakdown and resynthesis of phosphatidylcholine. J Biol Chem. 1986 Jul 15;261(20):9128–9132. [PubMed] [Google Scholar]
  6. Dixon J. F., Hokin L. E. Secretogogue-stimulated phosphatidylinositol breakdown in the exocrine pancreas liberates arachidonic acid, stearic acid, and glycerol by sequential actions of phospholipase C and diglyceride lipase. J Biol Chem. 1984 Dec 10;259(23):14418–14425. [PubMed] [Google Scholar]
  7. Emilsson A., Sundler R. Evidence for a catalytic role of phospholipase A in phorbol diester- and zymosan-induced mobilization of arachidonic acid in mouse peritoneal macrophages. Biochim Biophys Acta. 1986 May 21;876(3):533–542. doi: 10.1016/0005-2760(86)90041-x. [DOI] [PubMed] [Google Scholar]
  8. Flesch I., Ecker B., Ferber E. Acyltransferase-catalyzed cleavage of arachidonic acid from phospholipids and transfer to lysophosphatides in macrophages derived from bone marrow. Comparison of different donor- and acceptor substrate combinations. Eur J Biochem. 1984 Mar 15;139(3):431–437. doi: 10.1111/j.1432-1033.1984.tb08023.x. [DOI] [PubMed] [Google Scholar]
  9. Garcia-Gil M., Siraganian R. P. Source of the arachidonic acid released on stimulation of rat basophilic leukemia cells. J Immunol. 1986 May 15;136(10):3825–3828. [PubMed] [Google Scholar]
  10. Higgs G. A., Flower R. J., Vane J. R. A new approach to anti-inflammatory drugs. Biochem Pharmacol. 1979 Jun 15;28(12):1959–1961. doi: 10.1016/0006-2952(79)90651-8. [DOI] [PubMed] [Google Scholar]
  11. Hofmann S. L., Prescott S. M., Majerus P. W. The effects of mepacrine and p-bromophenacyl bromide on arachidonic acid release in human platelets. Arch Biochem Biophys. 1982 Apr 15;215(1):237–244. doi: 10.1016/0003-9861(82)90300-9. [DOI] [PubMed] [Google Scholar]
  12. Imai A., Yano K., Kameyama Y., Nozawa Y. Evidence for predominance of phospholipase A2 in release of arachidonic acid in thrombin-activated platelets: phosphatidylinositol-specific phospholipase C may play a minor role in arachidonate liberation. Jpn J Exp Med. 1982 Apr;52(2):99–105. [PubMed] [Google Scholar]
  13. Kannagi R., Koizumi K. Phospholipid-deacylating enzymes of rabbit platelets. Arch Biochem Biophys. 1979 Sep;196(2):534–542. doi: 10.1016/0003-9861(79)90305-9. [DOI] [PubMed] [Google Scholar]
  14. Lapetina E. G., Billah M. M., Cuatrecasas P. The initial action of thrombin on platelets. Conversion of phosphatidylinositol to phosphatidic acid preceding the production of arachidonic acid. J Biol Chem. 1981 May 25;256(10):5037–5040. [PubMed] [Google Scholar]
  15. Moscat J., Herrero C., Garcia-Barreno P., Municio A. M. Phospholipase C-diglyceride lipase is a major pathway for arachidonic acid release in macrophages. Biochem Biophys Res Commun. 1986 Nov 26;141(1):367–373. doi: 10.1016/s0006-291x(86)80378-3. [DOI] [PubMed] [Google Scholar]
  16. Okano Y., Ishizuka Y., Nakashima S., Tohmatsu T., Takagi H., Nozawa Y. Arachidonic acid release in rat peritoneal mast cells stimulated with antigen, ionophore A23187, and compound 48/80. Biochem Biophys Res Commun. 1985 Mar 29;127(3):726–732. doi: 10.1016/s0006-291x(85)80003-6. [DOI] [PubMed] [Google Scholar]
  17. Parker C. W. Allergic activation of mast cells. Arerugi. 1986 May;35(5):305–312. [PubMed] [Google Scholar]
  18. Prescott S. M., Majerus P. W. Characterization of 1,2-diacylglycerol hydrolysis in human platelets. Demonstration of an arachidonoyl-monoacylglycerol intermediate. J Biol Chem. 1983 Jan 25;258(2):764–769. [PubMed] [Google Scholar]
  19. 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]
  20. Strejan G., Campbell D. H. Hypersensitivity to Ascaris antigens. I. Skin-sensitizing activity of serum fractions from guinea pigs sensitized to crude extracts. J Immunol. 1967 May;98(5):893–900. [PubMed] [Google Scholar]
  21. Tada T., Okumura K. Regulation of homocytotropic antibody formation in the rat. I. Feed-back regulation by passively administered antibody. J Immunol. 1971 Apr;106(4):1002–1011. [PubMed] [Google Scholar]
  22. Takenawa T., Homma Y., Nagai Y. Role of Ca2+ in phosphatidylinositol response and arachidonic acid release in formylated tripeptide- or Ca2+ ionophore A23187-stimulated guinea pig neutrophils. J Immunol. 1983 Jun;130(6):2849–2855. [PubMed] [Google Scholar]
  23. 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 Mar 1;32(5):837–842. doi: 10.1016/0006-2952(83)90585-3. [DOI] [PubMed] [Google Scholar]
  24. Yamada K., Okano Y., Miura K., Nozawa Y. Arachidonic acid release in BW755C-pretreated rat peritoneal mast cells stimulated with A23187, concanavalin A and compound 48/80. Biochim Biophys Acta. 1987 Feb 14;917(2):290–295. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES