Abstract
Microorganisms cause varying degrees of stimulation of superoxide (O2-) production (respiratory burst [RB]) in macrophages but in some cases apparently inhibit the RB induced in the same monolayers by a conventional stimulator. We have explored these differences. A mycobacterium model, the slowly multiplying mouse pathogen Mycobacterium microti, induced a modest RB in resident macrophage monolayers, compared with the substantial RB induced by opsonized zymosan (Zy). However, if the 1-h M. microti pulse immediately preceded the Zy assay (instead of being concurrent), the RB was consistently less than that elicited by the Zy alone. Cytochalasin (an inhibitor of phagocytosis) enhanced Zy-induced RB, supporting the view that the burst is cell surface mediated, but this agent apparently eliminated the inhibition of the Zy-induced RB caused by prior M. microti exposure, suggesting that this inhibition may have an intracellular origin. The inhibition described extended not only to another mycobacterium (Mycobacterium bovis BCG) but also to a previous application of Zy itself. The general implications for macrophage functions of these observations on timing and sites of initiation are briefly discussed.
Full text
PDF

Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allison A. C., Davies P., De Petris S. Role of contractile microfilaments in macrophage movement and endocytosis. Nat New Biol. 1971 Aug 4;232(31):153–155. doi: 10.1038/newbio232153a0. [DOI] [PubMed] [Google Scholar]
- Brett S. J., Butler R. Interactions of Mycobacterium lepraemurium with resident peritoneal macrophages; phagocytosis and stimulation of the oxidative burst. Clin Exp Immunol. 1988 Jan;71(1):32–38. [PMC free article] [PubMed] [Google Scholar]
- Buchmüller-Rouiller Y., Mauël J. Impairment of the oxidative metabolism of mouse peritoneal macrophages by intracellular Leishmania spp. Infect Immun. 1987 Mar;55(3):587–593. doi: 10.1128/iai.55.3.587-593.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang H. R., Pechère J. C. Macrophage oxidative metabolism and intracellular Toxoplasma gondii. Microb Pathog. 1989 Jul;7(1):37–44. doi: 10.1016/0882-4010(89)90109-5. [DOI] [PubMed] [Google Scholar]
- Charnetzky W. T., Shuford W. W. Survival and growth of Yersinia pestis within macrophages and an effect of the loss of the 47-megadalton plasmid on growth in macrophages. Infect Immun. 1985 Jan;47(1):234–241. doi: 10.1128/iai.47.1.234-241.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deshpande R. G., Khan M. B., Savariar L. S., Windham Y. Z., Navalkar R. G. Superoxide dismutase activity of Mycobacterium avium complex (MAC) strains isolated from AIDS patients. Tuber Lung Dis. 1993 Oct;74(5):305–309. doi: 10.1016/0962-8479(93)90104-6. [DOI] [PubMed] [Google Scholar]
- Eissenberg L. G., Goldman W. E. Histoplasma capsulatum fails to trigger release of superoxide from macrophages. Infect Immun. 1987 Jan;55(1):29–34. doi: 10.1128/iai.55.1.29-34.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hart P. D., Young M. R., Gordon A. H., Sullivan K. H. Inhibition of phagosome-lysosome fusion in macrophages by certain mycobacteria can be explained by inhibition of lysosomal movements observed after phagocytosis. J Exp Med. 1987 Oct 1;166(4):933–946. doi: 10.1084/jem.166.4.933. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holzer T. J., Nelson K. E., Crispen R. G., Andersen B. R. Mycobacterium leprae fails to stimulate phagocytic cell superoxide anion generation. Infect Immun. 1986 Feb;51(2):514–520. doi: 10.1128/iai.51.2.514-520.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnston R. B., Jr, Lehmeyer J. E., Guthrie L. A. Generation of superoxide anion and chemiluminescence by human monocytes during phagocytosis and on contact with surface-bound immunoglobulin G. J Exp Med. 1976 Jun 1;143(6):1551–1556. doi: 10.1084/jem.143.6.1551. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCabe R. E., Mullins B. T. Failure of Trypanosoma cruzi to trigger the respiratory burst of activated macrophages. Mechanism for immune evasion and importance of oxygen-independent killing. J Immunol. 1990 Mar 15;144(6):2384–2388. [PubMed] [Google Scholar]
- Mor N., Goren M. B., Pabst M. J. Mycobacterium lepraemurium activates macrophages but fails to trigger release of superoxide anion. J Immunol. 1988 Jun 1;140(11):3956–3961. [PubMed] [Google Scholar]
- O'Brien S., Jackett P. S., Lowrie D. B., Andrew P. W. Guinea-pig alveolar macrophages kill Mycobacterium tuberculosis in vitro, but killing is independent of susceptibility to hydrogen peroxide or triggering of the respiratory burst. Microb Pathog. 1991 Mar;10(3):199–207. doi: 10.1016/0882-4010(91)90054-e. [DOI] [PubMed] [Google Scholar]
- Sugimoto M., Higuchi S., Ando M., Horio S., Tokuomi H. The effect of cytochalasin B on the superoxide production by alveolar macrophages obtained from normal rabbit lungs. J Reticuloendothel Soc. 1982 Feb;31(2):117–130. [PubMed] [Google Scholar]
- Wilson C. B., Tsai V., Remington J. S. Failure to trigger the oxidative metabolic burst by normal macrophages: possible mechanism for survival of intracellular pathogens. J Exp Med. 1980 Feb 1;151(2):328–346. doi: 10.1084/jem.151.2.328. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolf J. E., Kerchberger V., Kobayashi G. S., Little J. R. Modulation of the macrophage oxidative burst by Histoplasma capsulatum. J Immunol. 1987 Jan 15;138(2):582–586. [PubMed] [Google Scholar]