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. 1990 May 1;267(3):795–802. doi: 10.1042/bj2670795

Activation of superoxide formation and lysozyme release in human neutrophils by the synthetic lipopeptide Pam3Cys-Ser-(Lys)4. Involvement of guanine-nucleotide-binding proteins and synergism with chemotactic peptides.

R Seifert 1, G Schultz 1, M Richter-Freund 1, J Metzger 1, K H Wiesmüller 1, G Jung 1, W G Bessler 1, S Hauschildt 1
PMCID: PMC1131368  PMID: 2160237

Abstract

Upon exposure to the bacterial chemotactic peptide fMet-Leu-Phe, human neutrophils release lysozyme and generate superoxide anions (O2.-). The synthetic lipoamino acid N-palmitoyl-S-[2,3-bis(palmitoyloxy)-(2RS)-propyl]-(R)-cysteine (Pam3Cys), which is derived from the N-terminus of bacterial lipoprotein, when attached to Ser-(Lys)4 [giving Pam3Cys-Ser-(Lys)4], activated O2.- formation and lysozyme release in human neutrophils with an effectiveness amounting to about 15% of that of fMet-Leu-Phe. Palmitic acid, muramyl dipeptide, lipopolysaccharide and the lipopeptides Pam3Cys-Ala-Gly, Pam3Cys-Ser-Gly, Pam3Cys-Ser, Pam3Cys-OMe and Pam3Cys-OH did not activate O2.- formation. Pertussis toxin, which ADP-ribosylates guanine-nucleotide-binding proteins (G-proteins) and functionally uncouples formyl peptide receptors from G-proteins, prevented activation of O2.- formation by fMet-Leu-Phe and inhibited Pam3Cys-Ser-(Lys)4-induced O2.- formation by 85%. Lipopeptide-induced exocytosis was pertussis-toxin-insensitive. O2.- formation induced by Pam3Cys-Ser-(Lys)4 and fMet-Leu-Phe was enhanced by cytochalasin B, by a phorbol ester and by a diacylglycerol kinase inhibitor. Addition of activators of adenylate cyclase and removal of extracellular Ca2+ inhibited O2.- formation by fMet-Leu-Phe and Pam3Cys-Ser-(Lys)4 to different extents. Pam3Cys-Ser-(Lys)4 synergistically enhanced fMet-Leu-Phe-induced O2.- formation and primed neutrophils to respond to the chemotactic peptide at non-stimulatory concentrations. Our data suggest the following. (1) Pam3Cys-Ser-(Lys)4 activates neutrophils through G-proteins, involving pertussis-toxin-sensitive and -insensitive processes. (2) The signal transduction pathways activated by fMet-Leu-Phe and Pam3Cys-Ser-(Lys)4 are similar but not identical. (3) In inflammatory processes, bacterial lipoproteins and chemotactic peptides may interact synergistically to activate O2.- formation, leading to enhanced bactericidal activity.

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Selected References

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  1. Absolom D. R. Basic methods for the study of phagocytosis. Methods Enzymol. 1986;132:95–180. doi: 10.1016/s0076-6879(86)32005-6. [DOI] [PubMed] [Google Scholar]
  2. Ashkenazi A., Peralta E. G., Winslow J. W., Ramachandran J., Capon D. J. Functionally distinct G proteins selectively couple different receptors to PI hydrolysis in the same cell. Cell. 1989 Feb 10;56(3):487–493. doi: 10.1016/0092-8674(89)90251-1. [DOI] [PubMed] [Google Scholar]
  3. Bessler W. G., Cox M., Lex A., Suhr B., Wiesmüller K. H., Jung G. Synthetic lipopeptide analogs of bacterial lipoprotein are potent polyclonal activators for murine B lymphocytes. J Immunol. 1985 Sep;135(3):1900–1905. [PubMed] [Google Scholar]
  4. Biesert L., Scheuer W., Bessler W. G. Interaction of mitogenic bacterial lipoprotein and a synthetic analogue with mouse lymphocytes. Isolation and characterization of binding proteins. Eur J Biochem. 1987 Feb 2;162(3):651–657. doi: 10.1111/j.1432-1033.1987.tb10687.x. [DOI] [PubMed] [Google Scholar]
  5. Blackburn W. D., Jr, Heck L. W. Neutrophil activation by surface bound IgG: pertussis toxin insensitive activation. Biochem Biophys Res Commun. 1988 Apr 15;152(1):136–142. doi: 10.1016/s0006-291x(88)80690-9. [DOI] [PubMed] [Google Scholar]
  6. Bokoch G. M., Parkos C. A. Identification of novel GTP-binding proteins in the human neutrophil. FEBS Lett. 1988 Jan 18;227(1):66–70. doi: 10.1016/0014-5793(88)81415-7. [DOI] [PubMed] [Google Scholar]
  7. Braun V. Covalent lipoprotein from the outer membrane of Escherichia coli. Biochim Biophys Acta. 1975 Oct 31;415(3):335–377. doi: 10.1016/0304-4157(75)90013-1. [DOI] [PubMed] [Google Scholar]
  8. Burde R., Seifert R., Buschauer A., Schultz G. Histamine inhibits activation of human neutrophils and HL-60 leukemic cells via H2-receptors. Naunyn Schmiedebergs Arch Pharmacol. 1989 Dec;340(6):671–678. doi: 10.1007/BF00717743. [DOI] [PubMed] [Google Scholar]
  9. Dahinden C. A., Fehr J., Hugli T. E. Role of cell surface contact in the kinetics of superoxide production by granulocytes. J Clin Invest. 1983 Jul;72(1):113–121. doi: 10.1172/JCI110948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Deres K., Schild H., Wiesmüller K. H., Jung G., Rammensee H. G. In vivo priming of virus-specific cytotoxic T lymphocytes with synthetic lipopeptide vaccine. Nature. 1989 Nov 30;342(6249):561–564. doi: 10.1038/342561a0. [DOI] [PubMed] [Google Scholar]
  11. Dewald B., Baggiolini M. Activation of NADPH oxidase in human neutrophils. Synergism between fMLP and the neutrophil products PAF and LTB4. Biochem Biophys Res Commun. 1985 Apr 16;128(1):297–304. doi: 10.1016/0006-291x(85)91678-x. [DOI] [PubMed] [Google Scholar]
  12. Dubyak G. R., Cowen D. S., Meuller L. M. Activation of inositol phospholipid breakdown in HL60 cells by P2-purinergic receptors for extracellular ATP. Evidence for mediation by both pertussis toxin-sensitive and pertussis toxin-insensitive mechanisms. J Biol Chem. 1988 Dec 5;263(34):18108–18117. [PubMed] [Google Scholar]
  13. Forehand J. R., Pabst M. J., Phillips W. A., Johnston R. B., Jr Lipopolysaccharide priming of human neutrophils for an enhanced respiratory burst. Role of intracellular free calcium. J Clin Invest. 1989 Jan;83(1):74–83. doi: 10.1172/JCI113887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Gabler W. L., Creamer H. R., Bullock W. W. Fluoride activation of neutrophils: similarities to formylmethionyl-leucyl-phenylalanine. Inflammation. 1989 Feb;13(1):47–58. doi: 10.1007/BF00918962. [DOI] [PubMed] [Google Scholar]
  15. Guthrie L. A., McPhail L. C., Henson P. M., Johnston R. B., Jr Priming of neutrophils for enhanced release of oxygen metabolites by bacterial lipopolysaccharide. Evidence for increased activity of the superoxide-producing enzyme. J Exp Med. 1984 Dec 1;160(6):1656–1671. doi: 10.1084/jem.160.6.1656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hauschildt S., Hoffmann P., Beuscher H. U., Dufhues G., Heinrich P., Wiesmüller K. H., Jung G., Bessler W. G. Activation of bone marrow-derived mouse macrophages by bacterial lipopeptide: cytokine production, phagocytosis and Ia expression. Eur J Immunol. 1990 Jan;20(1):63–68. doi: 10.1002/eji.1830200110. [DOI] [PubMed] [Google Scholar]
  17. Hauschildt S., Steffens U., Wagner-Roos L., Bessler W. G. Role of proteinkinase C and phosphatidylinositol metabolism in lipopeptide-induced leukocyte activation as signal transducing mechanism. Mol Immunol. 1988 Nov;25(11):1081–1086. doi: 10.1016/0161-5890(88)90141-1. [DOI] [PubMed] [Google Scholar]
  18. Higashijima T., Uzu S., Nakajima T., Ross E. M. Mastoparan, a peptide toxin from wasp venom, mimics receptors by activating GTP-binding regulatory proteins (G proteins). J Biol Chem. 1988 May 15;263(14):6491–6494. [PubMed] [Google Scholar]
  19. Hoffmann P., Heinle S., Schade U. F., Loppnow H., Ulmer A. J., Flad H. D., Jung G., Bessler W. G. Stimulation of human and murine adherent cells by bacterial lipoprotein and synthetic lipopeptide analogues. Immunobiology. 1988 May;177(2):158–170. doi: 10.1016/S0171-2985(88)80036-6. [DOI] [PubMed] [Google Scholar]
  20. Jesaitis A. J., Tolley J. O., Allen R. A. Receptor-cytoskeleton interactions and membrane traffic may regulate chemoattractant-induced superoxide production in human granulocytes. J Biol Chem. 1986 Oct 15;261(29):13662–13669. [PubMed] [Google Scholar]
  21. Malech H. L., Gallin J. I. Current concepts: immunology. Neutrophils in human diseases. N Engl J Med. 1987 Sep 10;317(11):687–694. doi: 10.1056/NEJM198709103171107. [DOI] [PubMed] [Google Scholar]
  22. Markert M., Andrews P. C., Babior B. M. Measurement of O2- production by human neutrophils. The preparation and assay of NADPH oxidase-containing particles from human neutrophils. Methods Enzymol. 1984;105:358–365. doi: 10.1016/s0076-6879(84)05048-5. [DOI] [PubMed] [Google Scholar]
  23. McLeish K. R., Gierschik P., Schepers T., Sidiropoulos D., Jakobs K. H. Evidence that activation of a common G-protein by receptors for leukotriene B4 and N-formylmethionyl-leucyl-phenylalanine in HL-60 cells occurs by different mechanisms. Biochem J. 1989 Jun 1;260(2):427–434. doi: 10.1042/bj2600427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Melchers F., Braun V., Galanos C. The lipoprotein of the outer membrane of Escherichia coli: a B-lymphocyte mitogen. J Exp Med. 1975 Aug 1;142(2):473–482. doi: 10.1084/jem.142.2.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Nathan C. F. Neutrophil activation on biological surfaces. Massive secretion of hydrogen peroxide in response to products of macrophages and lymphocytes. J Clin Invest. 1987 Dec;80(6):1550–1560. doi: 10.1172/JCI113241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Okano Y., Takagi H., Tohmatsu T., Nakashima S., Kuroda Y., Saito K., Nozawa Y. A wasp venom mastoparan-induced polyphosphoinositide breakdown in rat peritoneal mast cells. FEBS Lett. 1985 Sep 2;188(2):363–366. doi: 10.1016/0014-5793(85)80403-8. [DOI] [PubMed] [Google Scholar]
  27. Prass W., Ringsdorf H., Bessler W., Wiesmüller K. H., Jung G. Lipopeptides of the N-terminus of Escherichia coli lipoprotein: synthesis, mitogenicity and properties in monolayer experiments. Biochim Biophys Acta. 1987 Jun 12;900(1):116–128. doi: 10.1016/0005-2736(87)90283-5. [DOI] [PubMed] [Google Scholar]
  28. Reitermann A., Metzger J., Wiesmüller K. H., Jung G., Bessler W. G. Lipopeptide derivatives of bacterial lipoprotein constitute potent immune adjuvants combined with or covalently coupled to antigen or hapten. Biol Chem Hoppe Seyler. 1989 Apr;370(4):343–352. doi: 10.1515/bchm3.1989.370.1.343. [DOI] [PubMed] [Google Scholar]
  29. Resch K., Bessler W. Activation of lymphocyte populations with concanavalin A or with lipoprotein and lipopeptide from the outer cell wall of Escherichia coli: correlation of early membrane changes with induction of macromolecular synthesis. Eur J Biochem. 1981 Apr;115(2):247–252. doi: 10.1111/j.1432-1033.1981.tb05230.x. [DOI] [PubMed] [Google Scholar]
  30. Richter J., Andersson T., Olsson I. Effect of tumor necrosis factor and granulocyte/macrophage colony-stimulating factor on neutrophil degranulation. J Immunol. 1989 May 1;142(9):3199–3205. [PubMed] [Google Scholar]
  31. Rossi F. The O2- -forming NADPH oxidase of the phagocytes: nature, mechanisms of activation and function. Biochim Biophys Acta. 1986 Nov 4;853(1):65–89. doi: 10.1016/0304-4173(86)90005-4. [DOI] [PubMed] [Google Scholar]
  32. Rüegg U. T., Burgess G. M. Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases. Trends Pharmacol Sci. 1989 Jun;10(6):218–220. doi: 10.1016/0165-6147(89)90263-0. [DOI] [PubMed] [Google Scholar]
  33. Schächtele C., Seifert R., Osswald H. Stimulus-dependent inhibition of platelet aggregation by the protein kinase C inhibitors polymyxin B, H-7 and staurosporine. Biochem Biophys Res Commun. 1988 Feb 29;151(1):542–547. doi: 10.1016/0006-291x(88)90628-6. [DOI] [PubMed] [Google Scholar]
  34. Seifert R., Burde R., Schultz G. Activation of NADPH oxidase by purine and pyrimidine nucleotides involves G proteins and is potentiated by chemotactic peptides. Biochem J. 1989 May 1;259(3):813–819. doi: 10.1042/bj2590813. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Seifert R., Burde R., Schultz G. Lack of effect of opioid peptides, morphine and naloxone on superoxide formation in human neutrophils and HL-60 leukemic cells. Naunyn Schmiedebergs Arch Pharmacol. 1989 Jul;340(1):101–106. doi: 10.1007/BF00169214. [DOI] [PubMed] [Google Scholar]
  36. Seifert R., Rosenthal W., Schultz G. Guanine nucleotides stimulate NADPH oxidase in membranes of human neutrophils. FEBS Lett. 1986 Sep 1;205(1):161–165. doi: 10.1016/0014-5793(86)80886-9. [DOI] [PubMed] [Google Scholar]
  37. Seifert R., Schultz G. Fatty-acid-induced activation of NADPH oxidase in plasma membranes of human neutrophils depends on neutrophil cytosol and is potentiated by stable guanine nucleotides. Eur J Biochem. 1987 Feb 2;162(3):563–569. doi: 10.1111/j.1432-1033.1987.tb10676.x. [DOI] [PubMed] [Google Scholar]
  38. Seifert R., Schultz G. Reversible activation of NADPH oxidase in membranes of HL-60 human leukemic cells. Biochem Biophys Res Commun. 1987 Aug 14;146(3):1296–1302. doi: 10.1016/0006-291x(87)90790-x. [DOI] [PubMed] [Google Scholar]
  39. Seifert R., Schächtele C. Studies with protein kinase C inhibitors presently available cannot elucidate the role of protein kinase C in the activation of NADPH oxidase. Biochem Biophys Res Commun. 1988 Apr 29;152(2):585–592. doi: 10.1016/s0006-291x(88)80078-0. [DOI] [PubMed] [Google Scholar]
  40. Seifert R., Wenzel K., Eckstein F., Schultz G. Purine and pyrimidine nucleotides potentiate activation of NADPH oxidase and degranulation by chemotactic peptides and induce aggregation of human neutrophils via G proteins. Eur J Biochem. 1989 Apr 15;181(1):277–285. doi: 10.1111/j.1432-1033.1989.tb14722.x. [DOI] [PubMed] [Google Scholar]
  41. Steffens U., Bessler W., Hauschild S. B cell activation by synthetic lipopeptide analogues of bacterial lipoprotein bypassing phosphatidylinositol metabolism and proteinkinase C translocation. Mol Immunol. 1989 Sep;26(9):897–904. doi: 10.1016/0161-5890(89)90146-6. [DOI] [PubMed] [Google Scholar]
  42. Tyagi S. R., Tamura M., Burnham D. N., Lambeth J. D. Phorbol myristate acetate (PMA) augments chemoattractant-induced diglyceride generation in human neutrophils but inhibits phosphoinositide hydrolysis. Implications for the mechanism of PMA priming of the respiratory burst. J Biol Chem. 1988 Sep 15;263(26):13191–13198. [PubMed] [Google Scholar]
  43. Wiesmüller K. H., Bessler W., Jung G. Synthesis of the mitogenic S-[2,3-bis(palmitoyloxy)propyl]-N-palmitoylpentapeptide from Escherichia coli lipoprotein. Hoppe Seylers Z Physiol Chem. 1983 May;364(5):593–606. doi: 10.1515/bchm2.1983.364.1.593. [DOI] [PubMed] [Google Scholar]
  44. Wilson S. P. Effects of mastoparan on catecholamine release from chromaffin cells. FEBS Lett. 1989 Apr 24;247(2):239–241. doi: 10.1016/0014-5793(89)81343-2. [DOI] [PubMed] [Google Scholar]
  45. Wojcikiewicz R. J., Nahorski S. R. Phosphoinositide hydrolysis in permeabilized SH-SY5Y human neuroblastoma cells is inhibited by mastoparan. FEBS Lett. 1989 Apr 24;247(2):341–344. doi: 10.1016/0014-5793(89)81366-3. [DOI] [PubMed] [Google Scholar]
  46. Yokokawa N., Komatsu M., Takeda T., Aizawa T., Yamada T. Mastoparan, a wasp venom, stimulates insulin release by pancreatic islets through pertussis toxin sensitive GTP-binding protein. Biochem Biophys Res Commun. 1989 Feb 15;158(3):712–716. doi: 10.1016/0006-291x(89)92779-4. [DOI] [PubMed] [Google Scholar]
  47. Yuo A., Kitagawa S., Suzuki I., Urabe A., Okabe T., Saito M., Takaku F. Tumor necrosis factor as an activator of human granulocytes. Potentiation of the metabolisms triggered by the Ca2+-mobilizing agonists. J Immunol. 1989 Mar 1;142(5):1678–1684. [PubMed] [Google Scholar]
  48. de Chaffoy de Courcelles D. C., Roevens P., Van Belle H. R 59 022, a diacylglycerol kinase inhibitor. Its effect on diacylglycerol and thrombin-induced C kinase activation in the intact platelet. J Biol Chem. 1985 Dec 15;260(29):15762–15770. [PubMed] [Google Scholar]

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