Skip to main content
Log in

Quartz-dust-induced production of reactive oxygen metabolites by human granulocytes

  • Published:
Lung Aims and scope Submit manuscript

Abstract

We studied the effect of quartz on the production of reactive oxygen species by human polymorphonuclear leukocytes (PMN) in vitro by a chemiluminescence (CL) assay. Quartz caused a rapid dose-dependent CL response in the cells. Diamond dust used as an inert control did not stimulate the production of reactive oxygen metabolites by PMN. The quartz-induced activation of oxygen metabolism was also demonstrated by measuring oxygen consumption, nitroblue tetrazolium reduction, and superoxide and hydrogen peroxide production by PMN. Poly-vinyl-pyridine N-oxide (a quartz surface modifying agent) completely abolished the quartz-induced response, but had no effect on opsonized zymosan-induced CL response of PMN. The effect of N-acetylcysteine (a known antioxidant) was inhibitory to the CL formation induced by both quartz and opsonized zymosan. Our results are in agreement with the hypothesis that quartz-induced production of reactive oxygen metabolites is a possible mechanism by which quartz dust produces chronic inflammation and tissue injury of the lung. Agents interfering with the generation of reactive oxygen metabolites may provide a rationale for treatment of mineral-dust-induced pulmonary disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Allison AC, Harrington JS, Birbeck M (1966) An examination of the cytotoxic effects of silica on macrophages. J Exp Med 124:141–154

    Article  PubMed  CAS  Google Scholar 

  2. Babior BM, Kipnes RS, Curnutte JT (1973) Biological defence mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent. J Clin Invest 52:741–744

    PubMed  CAS  Google Scholar 

  3. Bailey KR, Sheffner AL (1967) The reduction of experimentally induced inflammation by sulfhydryl compounds. Biochem Pharmacol 16:1175–1182

    Article  PubMed  CAS  Google Scholar 

  4. Bernard GR, Lucht WD, Niedermeyer ME, Snapper JR, Ogletree ML, Brogham KL (1984) Effect of N-acetylcysteine on the pulmonary response to endotoxin in the awake sheep and upon in vitro granulocyte function. J Clin Invest 73:1772–1784

    PubMed  CAS  Google Scholar 

  5. Böyum A (1968) Separation of leucocytes from blood and bone marrow. Scand J Clin Lab Invest 21:suppl 97

    Google Scholar 

  6. Cheson BD, Christensen RL, Sperling R, Kohler BE, Babior BM (1976) The origin of the chemiluminescence of phagocytosing granulocytes. J Clin Invest 58:789–796

    PubMed  CAS  Google Scholar 

  7. Dauber JH, Rossman MD, Peitra GG, Jimenez SA, Daniele RP (1980) Morphologic and biochemical abnormalities produced by the intracheal instillation of quartz. Am J Pathol 101:595–607

    PubMed  CAS  Google Scholar 

  8. Doll NJ, Stankus RP, Goldbach S, Salvaggio JE (1982) In vitro effect of asbestos fibers on polymorphonuclear leukocyte function. Int Arch Allergy Appl Immunol 68:17–21

    PubMed  CAS  Google Scholar 

  9. Fantone JC, Ward PA (1982) Role of oxygen-derived free radicals and metabolites in leukocyte-dependent inflammatory reactions. Am J Pathol 107:395–418

    PubMed  CAS  Google Scholar 

  10. Ferrante A, Nandoskar M, Bates EJ, Gor DHB (1987) Staphylococcus aureus-stimulated human mononuclear leucocyte-conditioned medium augments the basal and stimuli-induced neutrophil respiratory burst and degranulation. Immunology 60:431–438

    PubMed  CAS  Google Scholar 

  11. Freeman BA, Crapo JD (1982) Free radicals and tissue injury. Lab Invest 47:412–426

    PubMed  CAS  Google Scholar 

  12. Gee JB (1980) Cellular mechanisms in occupational lung disease. Chest 78:384–387

    PubMed  CAS  Google Scholar 

  13. Gupta GSD, Kaw JL (1982) Formation of lipid peroxides in the subcellular fractions of silicotic lungs in rats. Eur J Respir Dis 63:183–187

    PubMed  CAS  Google Scholar 

  14. Halliwell B, Gutteridge JMC (1984) Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J 291:1–14

    Google Scholar 

  15. Harington JS, Allison AC (1977) Tissue and cellular reactions to particles, fibers and aerosols retained after inhalation. In: Handbook of Physiology, Chapter 17, Section Editor: DHK Lee. American Physiological Society, Bethesda, Maryland, USA, 1977:263–283

    Google Scholar 

  16. Hedenborg M, Klockars M (1987) Asbestos fiber-induced production of reactive oxygen metabolites by human polymorphonuclear leukocytes. J Clin Pathol 40:1189–1193

    Article  PubMed  CAS  Google Scholar 

  17. Jahrstrand C (1977) The NBT (nitroblue tetrazolium) activity of neutrophil granulocytes in patients with influenza A infection. Scand J Infect Dis 9:5–7

    Google Scholar 

  18. Johnson KJ, Fantone JC, Kaplan J, Ward PA (1981) In vivo damage of rat lungs by oxygen metabolites. J Clin Invest 6:983–993

    Google Scholar 

  19. Keisari Y, Pick E (1981) Macrophage-mediated cytolysis of erythrocytes in the guinea pig: activation by stimulation of the oxidative burst. Cell Immunol 62:172–185

    Article  PubMed  CAS  Google Scholar 

  20. Langer AM, Nolan RP (1985) Physicochemical properties of minerals relevant to biological activities: State of the art. In: Beck EG, Bignon J (eds) In vitro effects of mineral dusts, Berlin Heidelberg: Springer-Verlag, pp 9–24

    Google Scholar 

  21. Lugano EM, Dauber JH, Daniele RP (1982) Acute experimental silicosis. Lung morphology, histology and macrophage chemotaxin secretion. Am J Pathol 109:27–36

    PubMed  CAS  Google Scholar 

  22. Margolis J, Margolis LS (1974) Silicosis—can the course of the disease be modified? Chest 66:107

    PubMed  CAS  Google Scholar 

  23. Moldéus P, Cotgrave IA, Berggren M (1986) Lung protection by a thiol-containing antioxidant: N-acetylcysteine. Respiration suppl 1:31–42

    Google Scholar 

  24. Morgan A, Moores RS, Holmes A, Evans JC, Evans NH, Black A (1980) The effect of quartz, administered by intratracheal instillation on the rat lung. I. The cellular response. Environ Res 22:1–12

    Article  PubMed  CAS  Google Scholar 

  25. Nash T, Allison AC, Harington JS (1966) Physicochemical properties of silica in relation to its toxicity. Nature 210:259–261

    Article  PubMed  CAS  Google Scholar 

  26. Osserman EF, Lawlor DP (1966) Serum and urinary lysozyme (muramidase) in monocytic and monomyelocytic leukemia. J Exp Med 124:921–952

    Article  PubMed  CAS  Google Scholar 

  27. Privalova LI, Katsnelson BA, Osipenko AB, Yushkow BN, Babuskina LC (1980) Response of a phagocyte cell system to products of macrophage breakdown as a probable mechanism of alveolar phagocytosis adaptation of deposition of particles of different cytotoxicity. Environ Health Perspect 35:205–218

    Article  PubMed  CAS  Google Scholar 

  28. Rook GAW, Steele J, Umar S, Dockrell HM (1985) A simple method for the solubilisation of reduced NBT, and its use as a colorimetric assay for activation of human macrophages byα-interferon. J Immunol Methods 82:161–167

    Article  PubMed  CAS  Google Scholar 

  29. Rossi F, Bellavite P, Berton G, Grzeskowiak M, Papini E (1985) Mechanism of production of toxic oxygen radicals by granulocytes and macrophages and their function in the inflammatory process. Pathol Res Pract 180:136–142

    PubMed  CAS  Google Scholar 

  30. Sachs T, Moldow CF, Craddock PR, Bowers JK, Jacob HS (1978) Oxygen radical mediated endothelial cell damage by complement-stimulated granulocytes: an in vitro model of immune vascular damage. J Clin Invest 61:1161–1167

    Article  Google Scholar 

  31. Tossavainen A (1979) Determination of quartz on membrane filters by x-ray diffraction. Scand J Work Environ Health 5:379–385

    PubMed  CAS  Google Scholar 

  32. Vilim V, Wilhelm J, Brzak P, Hurych J (1984) The chemiluminescence of rabbit alveolar macrophages induced by quartz dust particles. Immunol Lett 8:69–73

    Article  PubMed  CAS  Google Scholar 

  33. Weening RS, Roos D, Loos Jr (1974) Oxygen consumption of phagocytozing cells in human leukocyte and granulocyte preparations; a comparative study. J Lab Clin Med 83:570–576

    PubMed  CAS  Google Scholar 

  34. Weiss SJ, LoBuglio AF (1980) An oxygen dependent mechanism of neutrophil-mediated cytotoxicity. Blood 55:1020–1024

    PubMed  CAS  Google Scholar 

  35. Weitberg AB, Weitzman SA, Destrempes M, Latt SA, Stossel TP (1983) Stimulated human phagocytes produce cytogenetic changes in cultured mammalian cells. N Engl J Med 308:26–30

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hedenborg, M., Klockars, M. Quartz-dust-induced production of reactive oxygen metabolites by human granulocytes. Lung 167, 23–32 (1989). https://doi.org/10.1007/BF02714927

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02714927

Key words

Navigation