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. 1988 Oct;82(4):1376–1382. doi: 10.1172/JCI113741

Botulinum C2 toxin ADP-ribosylates actin and enhances O2- production and secretion but inhibits migration of activated human neutrophils.

J Norgauer 1, E Kownatzki 1, R Seifert 1, K Aktories 1
PMCID: PMC442694  PMID: 2844854

Abstract

The binary botulinum C2 toxin ADP-ribosylated the actin of human neutrophils. Treatment of human neutrophils with botulinum C2 toxin for 45 min increased FMLP-stimulated superoxide anion (O2-) production 1.5-5-fold, whereas only a minor fraction of the cellular actin pool (approximately 20%) was ADP-ribosylated. Effects of botulinum C2 toxin depended on toxin concentrations, presence of both components of the toxin, and incubation time. Cytochalasin B similarly enhanced O2- production. The effects of botulinum C2 toxin and cytochalasin B were additive at submaximally, but not maximally effective concentrations and incubation time of either toxin. Botulinum C2 toxin also enhanced stimulation of O2- production by Con A and platelet-activating factor, but not by phorbol 12-myristate 13-acetate (PMA). Botulinum C2 toxin increased FMLP-induced release of N-acetyl-glucosaminidase by 100-250%; release of vitamin B12-binding protein induced by FMLP and PMA was enhanced by approximately 150 and 50%, respectively. Botulinum C2 toxin blocked both random migration of neutrophils and migration induced by FMLP, complement C5a, leukotriene B4, and a novel monocyte-derived chemotactic agent. The data suggest that botulinum C2 toxin-catalyzed ADP-ribosylation of a minor actin pool has a pronounced effect on the activation of human neutrophils by various stimulants.

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Selected References

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  1. Aktories K., Ankenbauer T., Schering B., Jakobs K. H. ADP-ribosylation of platelet actin by botulinum C2 toxin. Eur J Biochem. 1986 Nov 17;161(1):155–162. doi: 10.1111/j.1432-1033.1986.tb10136.x. [DOI] [PubMed] [Google Scholar]
  2. Aktories K., Bärmann M., Ohishi I., Tsuyama S., Jakobs K. H., Habermann E. Botulinum C2 toxin ADP-ribosylates actin. Nature. 1986 Jul 24;322(6077):390–392. doi: 10.1038/322390a0. [DOI] [PubMed] [Google Scholar]
  3. Al-Mohanna F. A., Hallett M. B. Actin polymerization modifies stimulus-oxidase coupling in rat neutrophils. Biochim Biophys Acta. 1987 Mar 11;927(3):366–371. doi: 10.1016/0167-4889(87)90101-7. [DOI] [PubMed] [Google Scholar]
  4. Al-Mohanna F. A., Ohishi I., Hallett M. B. Botulinum C2 toxin potentiates activation of the neutrophil oxidase. Further evidence of a role for actin polymerization. FEBS Lett. 1987 Jul 13;219(1):40–44. doi: 10.1016/0014-5793(87)81187-0. [DOI] [PubMed] [Google Scholar]
  5. Bennett J. P., Cockcroft S., Gomperts B. D. Use of cytochalasin B to distinguish between early and late events in neutrophil activation. Biochim Biophys Acta. 1980 Oct 2;601(3):584–591. doi: 10.1016/0005-2736(80)90560-x. [DOI] [PubMed] [Google Scholar]
  6. Burgoyne R. D., Cheek T. R. Reorganisation of peripheral actin filaments as a prelude to exocytosis. Biosci Rep. 1987 Apr;7(4):281–288. doi: 10.1007/BF01121449. [DOI] [PubMed] [Google Scholar]
  7. Böttinger H., Reuner K. H., Aktories K. Inhibition of histamine release from rat mast cells by botulinum C2 toxin. Int Arch Allergy Appl Immunol. 1987;84(4):380–384. doi: 10.1159/000234453. [DOI] [PubMed] [Google Scholar]
  8. Cooper J. A. Effects of cytochalasin and phalloidin on actin. J Cell Biol. 1987 Oct;105(4):1473–1478. doi: 10.1083/jcb.105.4.1473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fehr J., Moser R., Leppert D., Groscurth P. Antiadhesive properties of biological surfaces are protective against stimulated granulocytes. J Clin Invest. 1985 Aug;76(2):535–542. doi: 10.1172/JCI112003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ingraham L. M., Coates T. D., Allen J. M., Higgins C. P., Baehner R. L., Boxer L. A. Metabolic, membrane, and functional responses of human polymorphonuclear leukocytes to platelet-activating factor. Blood. 1982 Jun;59(6):1259–1266. [PubMed] [Google Scholar]
  11. Jennings L. K., Fox J. E., Edwards H. H., Phillips D. R. Changes in the cytoskeletal structure of human platelets following thrombin activation. J Biol Chem. 1981 Jul 10;256(13):6927–6932. [PubMed] [Google Scholar]
  12. 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]
  13. Jesaitis A. J., Tolley J. O., Painter R. G., Sklar L. A., Cochrane C. G. Membrane-cytoskeleton interactions and the regulation of chemotactic peptide-induced activation of human granulocytes: the effects of dihydrocytochalasin B. J Cell Biochem. 1985;27(3):241–253. doi: 10.1002/jcb.240270306. [DOI] [PubMed] [Google Scholar]
  14. Kownatzki E., Kapp A., Uhrich S. Novel neutrophil chemotactic factor derived from human peripheral blood mononuclear leucocytes. Clin Exp Immunol. 1986 Apr;64(1):214–222. [PMC free article] [PubMed] [Google Scholar]
  15. Kownatzki E., Weil B., Uhrich S. The effects of bovine serum albumin and the chemotactic peptide formyl-methionyl-leucyl-phenylalanine on the adherence of guinea pig polymorphonuclear leukocytes to nylon fiber columns. Immunobiology. 1981;159(4-5):392–401. doi: 10.1016/s0171-2985(81)80095-2. [DOI] [PubMed] [Google Scholar]
  16. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  17. Lad P. M., Olson C. V., Grewal I. S. Role of a pertussis toxin substrate in the control of lectin-induced cap formation in human neutrophils. Biochem J. 1986 Aug 15;238(1):29–36. doi: 10.1042/bj2380029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. 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]
  19. O'Flaherty J. T., Schmitt J. D., Wykle R. L., Redman J. F., Jr, McCall C. E. Diacylglycerols and mezerein activate neutrophils by a phorbol myristate acetate-like mechanism. J Cell Physiol. 1985 Nov;125(2):192–199. doi: 10.1002/jcp.1041250204. [DOI] [PubMed] [Google Scholar]
  20. Ohishi I., Iwasaki M., Sakaguchi G. Purification and characterization of two components of botulinum C2 toxin. Infect Immun. 1980 Dec;30(3):668–673. doi: 10.1128/iai.30.3.668-673.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Omann G. M., Allen R. A., Bokoch G. M., Painter R. G., Traynor A. E., Sklar L. A. Signal transduction and cytoskeletal activation in the neutrophil. Physiol Rev. 1987 Jan;67(1):285–322. doi: 10.1152/physrev.1987.67.1.285. [DOI] [PubMed] [Google Scholar]
  22. Reuner K. H., Presek P., Boschek C. B., Aktories K. Botulinum C2 toxin ADP-ribosylates actin and disorganizes the microfilament network in intact cells. Eur J Cell Biol. 1987 Feb;43(1):134–140. [PubMed] [Google Scholar]
  23. Rider L. G., Niedel J. E. Diacylglycerol accumulation and superoxide anion production in stimulated human neutrophils. J Biol Chem. 1987 Apr 25;262(12):5603–5608. [PubMed] [Google Scholar]
  24. 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]
  25. Singer S. J., Kupfer A. The directed migration of eukaryotic cells. Annu Rev Cell Biol. 1986;2:337–365. doi: 10.1146/annurev.cb.02.110186.002005. [DOI] [PubMed] [Google Scholar]
  26. Sklar L. A., Omann G. M., Painter R. G. Relationship of actin polymerization and depolymerization to light scattering in human neutrophils: dependence on receptor occupancy and intracellular Ca++. J Cell Biol. 1985 Sep;101(3):1161–1166. doi: 10.1083/jcb.101.3.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Vandekerckhove J., Schering B., Bärmann M., Aktories K. Clostridium perfringens iota toxin ADP-ribosylates skeletal muscle actin in Arg-177. FEBS Lett. 1987 Dec 10;225(1-2):48–52. doi: 10.1016/0014-5793(87)81129-8. [DOI] [PubMed] [Google Scholar]
  28. White J. R., Naccache P. H., Sha'afi R. I. Stimulation by chemotactic factor of actin association with the cytoskeleton in rabbit neutrophils. Effects of calcium and cytochalasin B. J Biol Chem. 1983 Nov 25;258(22):14041–14047. [PubMed] [Google Scholar]

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