Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1990 Dec 1;111(6):2885–2891. doi: 10.1083/jcb.111.6.2885

Neomycin is a potent secretagogue of mast cells that directly activates a GTP-binding protein involved in exocytosis

PMCID: PMC2116356  PMID: 1702786

Abstract

When loaded alongside GTP-gamma-S into ATP-permeabilized cells, neomycin, at concentrations below 1 mM, inhibits GTP-gamma-S-induced histamine secretion and phosphatidic acid formation (Cockcroft, S., and B. D. Gomperts, 1985. Nature (Lond.). 314: 534-536; Aridor, M., L. M. Traub, and R. Sagi-Eisenberg. 1990. J. Cell Biol. 111:909-917). However, at higher concentrations internally applied neomycin induces histamine secretion in a process that is: (a) dose dependent; (b) dependent on the internal application of GTP; (c) independent of phosphoinositide breakdown; and (d) inhibited by pertussis toxin (PtX) treatment. These results indicate that neomycin can stimulate histamine secretion in a mechanism that bypasses phospholipase C (PLC) activation and yet involves a PtX-sensitive GTP-binding protein (G protein). Unlike its dual effects, when internally applied, neomycin induces histamine secretion from intact mast cells in a dose-dependent manner. Half-maximal and maximal effects are obtained at 0.5 and 1 mM neomycin, respectively. This process is rapid (approximately 30 s), is independent of external Ca2+, and is associated with phosphatidic acid formation, implying that neomycin can activate histamine secretion by a mechanism similar to that utilized by other basic secretagogues of mast cells. Neomycin stimulates fourfold the GTPase activity of cholate- solubilized rat brain membranes in a PtX-inhibitable manner. In addition neomycin, as well as the basic secretagogues of mast cells, compound 48/80, and mastoparan, significantly reduce (by approximately 80%) the ADP ribosylation of PtX substrates present in rat brain membranes. Taken together these data suggest that neomycin can stimulate secretion from mast cells by directly activating G proteins that play a role in stimulus-secretion coupling. When internally applied, neomycin presumably stimulates secretion by activating a G protein that is located downstream to PLC. This G protein serves as a substrate for PtX.

Full Text

The Full Text of this article is available as a PDF (989.9 KB).

Selected References

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

  1. Aridor M., Traub L. M., Sagi-Eisenberg R. Exocytosis in mast cells by basic secretagogues: evidence for direct activation of GTP-binding proteins. J Cell Biol. 1990 Sep;111(3):909–917. doi: 10.1083/jcb.111.3.909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. 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]
  3. Barrowman M. M., Cockcroft S., Gomperts B. D. Two roles for guanine nucleotides in the stimulus-secretion sequence of neutrophils. Nature. 1986 Feb 6;319(6053):504–507. doi: 10.1038/319504a0. [DOI] [PubMed] [Google Scholar]
  4. Cockcroft S., Gomperts B. D. Role of guanine nucleotide binding protein in the activation of polyphosphoinositide phosphodiesterase. Nature. 1985 Apr 11;314(6011):534–536. doi: 10.1038/314534a0. [DOI] [PubMed] [Google Scholar]
  5. 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]
  6. Fernandez J. M., Neher E., Gomperts B. D. Capacitance measurements reveal stepwise fusion events in degranulating mast cells. 1984 Nov 29-Dec 5Nature. 312(5993):453–455. doi: 10.1038/312453a0. [DOI] [PubMed] [Google Scholar]
  7. Fewtrell C. M., Foreman J. C., Jordan C. C., Oehme P., Renner H., Stewart J. M. The effects of substance P on histamine and 5-hydroxytryptamine release in the rat. J Physiol. 1982 Sep;330:393–411. doi: 10.1113/jphysiol.1982.sp014347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gibbs J. B., Schaber M. D., Allard W. J., Sigal I. S., Scolnick E. M. Purification of ras GTPase activating protein from bovine brain. Proc Natl Acad Sci U S A. 1988 Jul;85(14):5026–5030. doi: 10.1073/pnas.85.14.5026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gomperts B. D. Involvement of guanine nucleotide-binding protein in the gating of Ca2+ by receptors. Nature. 1983 Nov 3;306(5938):64–66. doi: 10.1038/306064a0. [DOI] [PubMed] [Google Scholar]
  10. Herrmann E., Gierschik P., Jakobs K. H. Neomycin induces high-affinity agonist binding of G-protein-coupled receptors. Eur J Biochem. 1989 Nov 20;185(3):677–683. doi: 10.1111/j.1432-1033.1989.tb15165.x. [DOI] [PubMed] [Google Scholar]
  11. Herrmann E., Jakobs K. H. Stimulation and inhibition of human platelet membrane high-affinity GTPase by neomycin. FEBS Lett. 1988 Feb 29;229(1):49–53. doi: 10.1016/0014-5793(88)80795-6. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Howell T. W., Cockcroft S., Gomperts B. D. Essential synergy between Ca2+ and guanine nucleotides in exocytotic secretion from permeabilized rat mast cells. J Cell Biol. 1987 Jul;105(1):191–197. doi: 10.1083/jcb.105.1.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Katada T., Oinuma M., Ui M. Two guanine nucleotide-binding proteins in rat brain serving as the specific substrate of islet-activating protein, pertussis toxin. Interaction of the alpha-subunits with beta gamma-subunits in development of their biological activities. J Biol Chem. 1986 Jun 25;261(18):8182–8191. [PubMed] [Google Scholar]
  15. Mousli M., Bronner C., Landry Y., Bockaert J., Rouot B. Direct activation of GTP-binding regulatory proteins (G-proteins) by substance P and compound 48/80. FEBS Lett. 1990 Jan 1;259(2):260–262. doi: 10.1016/0014-5793(90)80023-c. [DOI] [PubMed] [Google Scholar]
  16. Nakashima S., Tohmatsu T., Shirato L., Takenaka A., Nozawa Y. Neomycin is a potent agent for arachidonic acid release in human platelets. Biochem Biophys Res Commun. 1987 Jul 31;146(2):820–826. doi: 10.1016/0006-291x(87)90604-8. [DOI] [PubMed] [Google Scholar]
  17. Ohki S., Düzgüneş N., Leonards K. Phospholipid vesicle aggregation: effect of monovalent and divalent ions. Biochemistry. 1982 Apr 27;21(9):2127–2133. doi: 10.1021/bi00538a022. [DOI] [PubMed] [Google Scholar]
  18. Polascik T., Godfrey P. P., Watson S. P. Neomycin cannot be used as a selective inhibitor of inositol phospholipid hydrolysis in intact or semi-permeabilized human platelets. Aminoglycosides activate semi-permeabilized platelets. Biochem J. 1987 May 1;243(3):815–819. doi: 10.1042/bj2430815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Repke H., Piotrowski W., Bienert M., Foreman J. C. Histamine release induced by Arg-Pro-Lys-Pro(CH2)11CH3 from rat peritoneal mast cells. J Pharmacol Exp Ther. 1987 Oct;243(1):317–321. [PubMed] [Google Scholar]
  20. Sagi-Eisenberg R., Ben-Neriah Z., Pecht I., Terry S., Blumberg S. Structure-activity relationship in the mast cell degranulating capacity of neurotensin fragments. Neuropharmacology. 1983 Feb;22(2):197–201. doi: 10.1016/0028-3908(83)90009-6. [DOI] [PubMed] [Google Scholar]
  21. Sagi-Eisenberg R., Foreman J. C., Shelly R. Histamine release induced by histone and phorbol ester from rat peritoneal mast cells. Eur J Pharmacol. 1985 Jul 11;113(1):11–17. doi: 10.1016/0014-2999(85)90337-1. [DOI] [PubMed] [Google Scholar]
  22. Sargent D. F., Schwyzer R. Membrane lipid phase as catalyst for peptide-receptor interactions. Proc Natl Acad Sci U S A. 1986 Aug;83(16):5774–5778. doi: 10.1073/pnas.83.16.5774. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schacht J. Purification of polyphosphoinositides by chromatography on immobilized neomycin. J Lipid Res. 1978 Nov;19(8):1063–1067. [PubMed] [Google Scholar]
  24. Shibata H., Mio M., Tasaka K. Analysis of the mechanism of histamine release induced by substance P. Biochim Biophys Acta. 1985 Jul 30;846(1):1–7. doi: 10.1016/0167-4889(85)90102-8. [DOI] [PubMed] [Google Scholar]
  25. Shibata H., Mio M., Tasaka K. Permeability increase in black lipid membrane induced by compound 48/80. Biochim Biophys Acta. 1984 Sep 14;805(1):127–130. doi: 10.1016/0167-4889(84)90045-4. [DOI] [PubMed] [Google Scholar]
  26. Siess W., Lapetina E. G. Neomycin inhibits inositol phosphate formation in human platelets stimulated by thrombin but not other agonists. FEBS Lett. 1986 Oct 20;207(1):53–57. doi: 10.1016/0014-5793(86)80011-4. [DOI] [PubMed] [Google Scholar]
  27. 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]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES