Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1981 May 1;195(2):427–433. doi: 10.1042/bj1950427

[Identification and characterization of two phospholipase A2 activities in resident mouse peritoneal macrophages.]

P D Wightman, J L Humes, P Davies, R J Bonney
PMCID: PMC1162906  PMID: 7316959

Abstract

Resident mouse peritoneal macrophages synthesize and release large amounts of prostaglandins in response to inflammatory stimuli. Release of prostaglandin E2 and 6-oxoprostaglandin F1 alpha occurs at a rate of 1 nmol/h per mg of cell protein. The mechanisms by which substrate arachidonic acid is released have yet to be established. We have therefore initiated studies to characterize those enzymes that can catalyse its release from phospholipid and may be of significance at the cellular level. We report initially the characterization of two phospholipase A2 activities in homogenates of mouse peritoneal macrophages. The first is active at pH 4.5 and is not dependent on Ca2+. The second is Ca2+-dependent and is optimally active at pH 8.5. Either phospholipase A2 activity is capable of hydrolysing [14C] arachidonic acid from [14C] arachidonic acid-labelled phospholipids in quantities sufficient to account for the amounts of prostaglandins by macrophages in culture. Phospholipid substrates are prepared from mouse LM fibroblasts in serum-free Higuchi medium containing radiolabelled phospholipid precursors. Single-labelled phospholipids bear the 14C label in the arachidonic acid moiety. Dual-labelled phospholipids bear a 14C label in the polar head group and a 3H label in the arachidonic acid moiety. Experiments with dual-labelled substrates establish that both phospholipase activities are of the A2 type as indicated by the equimolar recovery of [3H] arachidonic acid and [14C] lysophospholipid. Studies with aqueous sonicated dispersions of purified [14C] arachidonic acid-labelled phospholipid or mixed liposomal substrates formed from mixtures of cellular polar lipids reveal that the pH 4.5 activity hydrolyses phosphatidylethanolamine and phosphatidylcholine more efficiently when they are present in a mixture of other polar lipids. The pH 8.5 activity, however, hydrolyses the purified phospholipids more efficiently.

Full text

PDF
427

Selected References

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

  1. Adamich M., Roberts M. F., Dennis E. A. Phospholipid activation of cobra venom phospholipase A2. 2. Characterization of the phospholipid--enzyme interaction. Biochemistry. 1979 Jul 24;18(15):3308–3314. doi: 10.1021/bi00582a017. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Bell R. L., Kennerly D. A., Stanford N., Majerus P. W. Diglyceride lipase: a pathway for arachidonate release from human platelets. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3238–3241. doi: 10.1073/pnas.76.7.3238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bonney R. J., Naruns P., Davies P., Humes J. L. Antigen-antibody complexes stimulate the synthesis and release of prostaglandins by mouse peritoneal macrophages. Prostaglandins. 1979 Oct;18(4):605–616. doi: 10.1016/0090-6980(79)90027-3. [DOI] [PubMed] [Google Scholar]
  5. Bonney R. J., Wightman P. D., Davies P., Sadowski S. J., Kuehl F. A., Jr, Humes J. L. Regulation of prostaglandin synthesis and of the selective release of lysosomal hydrolases by mouse peritoneal macrophages. Biochem J. 1978 Nov 15;176(2):433–442. doi: 10.1042/bj1760433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bonney R. J., Wightman P. D., Davies P. Selective inhibitors of lecithin biosynthesis in mouse peritoneal macrophages. Biochem Pharmacol. 1979 Aug 15;28(16):2471–2478. doi: 10.1016/0006-2952(79)90010-8. [DOI] [PubMed] [Google Scholar]
  7. Brune K., Glatt M., Kälin H., Peskar B. A. Pharmacological control of prostaglandin and thromboxane release from macrophages. Nature. 1978 Jul 20;274(5668):261–263. doi: 10.1038/274261a0. [DOI] [PubMed] [Google Scholar]
  8. Chap H., Douste-Blazy L. Réaction de libération plaquettaire induite par la phospholipase C. Eur J Biochem. 1974 Oct 2;48(2):351–355. doi: 10.1111/j.1432-1033.1974.tb03776.x. [DOI] [PubMed] [Google Scholar]
  9. Franson R. C., Waite M. Lysosomal phospholipase A 1 and A 2 of normal and bacillus calmette guerin-induced alveolar macrophages. J Cell Biol. 1973 Mar;56(3):621–627. doi: 10.1083/jcb.56.3.621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Franson R., Waite M. Relation between calcium requirement, substrate charge, and rabbit polymorphonuclear leukocyte phospholipase A2 activity. Biochemistry. 1978 Sep 19;17(19):4029–4033. doi: 10.1021/bi00612a024. [DOI] [PubMed] [Google Scholar]
  11. Franson R., Waite M., Weglicki W. Phospholipase A activity of lysosomes of rat myocardial tissue. Biochemistry. 1972 Feb 1;11(3):472–476. doi: 10.1021/bi00753a028. [DOI] [PubMed] [Google Scholar]
  12. Gatt S., Barenholz Y. Enzymes of complex lipid metabolism. Annu Rev Biochem. 1973;42(0):61–90. doi: 10.1146/annurev.bi.42.070173.000425. [DOI] [PubMed] [Google Scholar]
  13. Helenius A., Simons K. Solubilization of membranes by detergents. Biochim Biophys Acta. 1975 Mar 25;415(1):29–79. doi: 10.1016/0304-4157(75)90016-7. [DOI] [PubMed] [Google Scholar]
  14. Humes J. L., Bonney R. J., Pelus L., Dahlgren M. E., Sadowski S. J., Kuehl F. A., Jr, Davies P. Macrophages synthesis and release prostaglandins in response to inflammatory stimuli. Nature. 1977 Sep 8;269(5624):149–151. doi: 10.1038/269149a0. [DOI] [PubMed] [Google Scholar]
  15. Kraml M. A semi-automated determination of phospholipids. Clin Chim Acta. 1966 Apr;13(4):442–448. doi: 10.1016/0009-8981(66)90235-x. [DOI] [PubMed] [Google Scholar]
  16. Kunze H., Vogt W. Significance of phospholipase A for prostaglandin formation. Ann N Y Acad Sci. 1971 Apr 30;180:123–125. doi: 10.1111/j.1749-6632.1971.tb53191.x. [DOI] [PubMed] [Google Scholar]
  17. Lapetina E. G., Cuatrecasas P. Stimulation of phosphatidic acid production in platelets precedes the formation of arachidonate and parallels the release of serotonin. Biochim Biophys Acta. 1979 May 25;573(2):394–402. doi: 10.1016/0005-2760(79)90072-9. [DOI] [PubMed] [Google Scholar]
  18. Mason R. J., Stossel T. P., Vaughan M. Lipids of alveolar macrophages, polymorphonuclear leukocytes, and their phagocytic vesicles. J Clin Invest. 1972 Sep;51(9):2399–2407. doi: 10.1172/JCI107052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Mauco G., Chap H., Douste-Blazy L. Characterization and properties of a phosphatidylinositol phosphodiesterase (phospholipase C) from platelet cytosol. FEBS Lett. 1979 Apr 15;100(2):367–370. doi: 10.1016/0014-5793(79)80371-3. [DOI] [PubMed] [Google Scholar]
  20. McMurray W. C., Magee W. L. Phospholipid metabolism. Annu Rev Biochem. 1972;41(10):129–160. doi: 10.1146/annurev.bi.41.070172.001021. [DOI] [PubMed] [Google Scholar]
  21. Nachbaur J., Colbeau A., Vignais P. M. Distribution of membrane-confined phospholipases A in the rat hepatocyte. Biochim Biophys Acta. 1972 Aug 9;274(2):426–446. doi: 10.1016/0005-2736(72)90189-7. [DOI] [PubMed] [Google Scholar]
  22. Nieuwenhuizen W., Kunze H., de Haas G. H. Phospholipase A2 (phosphatide acylhydrolase, EC 3.1.1.4) from porcine pancreas. Methods Enzymol. 1974;32:147–154. doi: 10.1016/0076-6879(74)32018-6. [DOI] [PubMed] [Google Scholar]
  23. Rittenhouse-Simmons S. Production of diglyceride from phosphatidylinositol in activated human platelets. J Clin Invest. 1979 Apr;63(4):580–587. doi: 10.1172/JCI109339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stossel T. P., Mason R. J., Smith A. L. Lipid peroxidation by human blood phagocytes. J Clin Invest. 1974 Sep;54(3):638–645. doi: 10.1172/JCI107801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Tyson C. A., Vande Zande H., Green D. E. Phospholipids as ionophores. J Biol Chem. 1976 Mar 10;251(5):1326–1332. [PubMed] [Google Scholar]
  26. Verkleij A. J., Zwaal R. F., Roelofsen B., Comfurius P., Kastelijn D., van Deenen L. L. The asymmetric distribution of phospholipids in the human red cell membrane. A combined study using phospholipases and freeze-etch electron microscopy. Biochim Biophys Acta. 1973 Oct 11;323(2):178–193. doi: 10.1016/0005-2736(73)90143-0. [DOI] [PubMed] [Google Scholar]
  27. Waite M., Scherphof G. L., Boshouwers F. M., van Deenen L. L. Differentiation of phospholipases A in mitochondria and lysosomes of rat liver. J Lipid Res. 1969 Jul;10(4):411–420. [PubMed] [Google Scholar]
  28. Waite M., van Deenen L. L. Hydrolysis of phospholipids and glycerides by rat-liver preparations. Biochim Biophys Acta. 1967 Jun 6;137(3):498–517. doi: 10.1016/0005-2760(67)90131-2. [DOI] [PubMed] [Google Scholar]
  29. Ziboh V. A., Lord J. T. Phospholipase A activity in the skin. Modulators of arachidonic acid release from phosphatidylcholine. Biochem J. 1979 Nov 15;184(2):283–290. doi: 10.1042/bj1840283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. van den Bosch H. Phosphoglyceride metabolism. Annu Rev Biochem. 1974;43(0):243–277. doi: 10.1146/annurev.bi.43.070174.001331. [DOI] [PubMed] [Google Scholar]

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

RESOURCES