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. 2000 Jul 1;349(Pt 1):99–104. doi: 10.1042/0264-6021:3490099

Indirect induction of suppressor of cytokine signalling-1 in macrophages stimulated with bacterial lipopolysaccharide: partial role of autocrine/paracrine interferon-alpha/beta.

A Crespo 1, M B Filla 1, S W Russell 1, W J Murphy 1
PMCID: PMC1221125  PMID: 10861216

Abstract

It has previously been reported by us that a brief prior exposure of mouse bone marrow culture-derived macrophages to bacterial lipopolysaccharide (LPS) resulted in a dramatic reduction in their ability to produce NO in response to a subsequent stimulus with either interferon-gamma (IFN-gamma) or IFN-gamma plus LPS. We show here that this brief exposure to LPS results in an impaired response to subsequently added IFN-gamma. A 2--4 h pretreatment with LPS leads to a dramatic reduction in the IFN-gamma-induced DNA-binding of the transcription factor, signal transducer and activator of transcription 1 alpha (STAT1 alpha). This loss in ability to activate STAT1 alpha temporally correlates with the LPS-induced accumulation of mRNA encoding the suppressor of cytokine signalling-1 (SOCS-1). However, LPS does not directly induce the synthesis of SOCS-1. Rather, LPS induces the synthesis of autocrine/paracrine factors that are the true mediators of SOCS-1 induction. IFN-alpha/beta is one of these mediators, but plays only a partial role in the induction of SOCS-1 because neutralization of LPS-induced IFN-alpha/beta production incompletely inhibits the induction of SOCS-1. We show that mouse IFN-beta directly induces the synthesis of SOCS-1, without the need for prior protein synthesis, and does so with faster kinetics than does LPS. Our results are consistent with the non-specific nature of LPS-induced tolerance and provide a mechanistic insight into nonspecificity; LPS indirectly induces the synthesis of a protein mediator, SOCS-1, which inhibits the signalling that is induced by IFN-gamma.

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Selected References

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  1. Alexander W. S., Starr R., Fenner J. E., Scott C. L., Handman E., Sprigg N. S., Corbin J. E., Cornish A. L., Darwiche R., Owczarek C. M. SOCS1 is a critical inhibitor of interferon gamma signaling and prevents the potentially fatal neonatal actions of this cytokine. Cell. 1999 Sep 3;98(5):597–608. doi: 10.1016/s0092-8674(00)80047-1. [DOI] [PubMed] [Google Scholar]
  2. Barber S. A., Fultz M. J., Salkowski C. A., Vogel S. N. Differential expression of interferon regulatory factor 1 (IRF-1), IRF-2, and interferon consensus sequence binding protein genes in lipopolysaccharide (LPS)-responsive and LPS-hyporesponsive macrophages. Infect Immun. 1995 Feb;63(2):601–608. doi: 10.1128/iai.63.2.601-608.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berczi I. Neurohormonal host defense in endotoxin shock. Ann N Y Acad Sci. 1998 May 1;840:787–802. doi: 10.1111/j.1749-6632.1998.tb09617.x. [DOI] [PubMed] [Google Scholar]
  4. Blackwell T. S., Blackwell T. R., Christman J. W. Induction of endotoxin tolerance depletes nuclear factor-kappaB and suppresses its activation in rat alveolar macrophages. J Leukoc Biol. 1997 Dec;62(6):885–891. doi: 10.1002/jlb.62.6.885. [DOI] [PubMed] [Google Scholar]
  5. Bode J. G., Nimmesgern A., Schmitz J., Schaper F., Schmitt M., Frisch W., Häussinger D., Heinrich P. C., Graeve L. LPS and TNFalpha induce SOCS3 mRNA and inhibit IL-6-induced activation of STAT3 in macrophages. FEBS Lett. 1999 Dec 17;463(3):365–370. doi: 10.1016/s0014-5793(99)01662-2. [DOI] [PubMed] [Google Scholar]
  6. Carvalho G. L., Wakabayashi G., Shimazu M., Karahashi T., Yoshida M., Yamamoto S., Matsushima K., Mukaida N., Clark B. D., Takabayashi T. Anti-interleukin-8 monoclonal antibody reduces free radical production and improves hemodynamics and survival rate in endotoxic shock in rabbits. Surgery. 1997 Jul;122(1):60–68. doi: 10.1016/s0039-6060(97)90265-8. [DOI] [PubMed] [Google Scholar]
  7. Cavaillon J. M. The nonspecific nature of endotoxin tolerance. Trends Microbiol. 1995 Aug;3(8):320–324. doi: 10.1016/s0966-842x(00)88963-5. [DOI] [PubMed] [Google Scholar]
  8. Chang C. C., McCormick C. C., Lin A. W., Dietert R. R., Sung Y. J. Inhibition of nitric oxide synthase gene expression in vivo and in vitro by repeated doses of endotoxin. Am J Physiol. 1996 Oct;271(4 Pt 1):G539–G548. doi: 10.1152/ajpgi.1996.271.4.G539. [DOI] [PubMed] [Google Scholar]
  9. Dickensheets H. L., Venkataraman C., Schindler U., Donnelly R. P. Interferons inhibit activation of STAT6 by interleukin 4 in human monocytes by inducing SOCS-1 gene expression. Proc Natl Acad Sci U S A. 1999 Sep 14;96(19):10800–10805. doi: 10.1073/pnas.96.19.10800. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fahmi H., Chaby R. Selective refractoriness of macrophages to endotoxin-induced production of tumor necrosis factor, elicited by an autocrine mechanism. J Leukoc Biol. 1993 Jan;53(1):45–52. doi: 10.1002/jlb.53.1.45. [DOI] [PubMed] [Google Scholar]
  11. Fujihara M., Ito N., Pace J. L., Watanabe Y., Russell S. W., Suzuki T. Role of endogenous interferon-beta in lipopolysaccharide-triggered activation of the inducible nitric-oxide synthase gene in a mouse macrophage cell line, J774. J Biol Chem. 1994 Apr 29;269(17):12773–12778. [PubMed] [Google Scholar]
  12. Gao J. J., Filla M. B., Fultz M. J., Vogel S. N., Russell S. W., Murphy W. J. Autocrine/paracrine IFN-alphabeta mediates the lipopolysaccharide-induced activation of transcription factor Stat1alpha in mouse macrophages: pivotal role of Stat1alpha in induction of the inducible nitric oxide synthase gene. J Immunol. 1998 Nov 1;161(9):4803–4810. [PubMed] [Google Scholar]
  13. Gao J., Morrison D. C., Parmely T. J., Russell S. W., Murphy W. J. An interferon-gamma-activated site (GAS) is necessary for full expression of the mouse iNOS gene in response to interferon-gamma and lipopolysaccharide. J Biol Chem. 1997 Jan 10;272(2):1226–1230. doi: 10.1074/jbc.272.2.1226. [DOI] [PubMed] [Google Scholar]
  14. Gonnella P. A., Starr S., Rodrick M. L., Wilmore D. W. Induced hyporesponsiveness in rat Kupffer cells is not specific for lipopolysaccharide. Immunology. 1994 Mar;81(3):402–406. [PMC free article] [PubMed] [Google Scholar]
  15. Granowitz E. V., Porat R., Mier J. W., Orencole S. F., Kaplanski G., Lynch E. A., Ye K., Vannier E., Wolff S. M., Dinarello C. A. Intravenous endotoxin suppresses the cytokine response of peripheral blood mononuclear cells of healthy humans. J Immunol. 1993 Aug 1;151(3):1637–1645. [PubMed] [Google Scholar]
  16. Haas J. G., Meyer N., Riethmüller G., Ziegler-Heitbrock H. W. Inhibition of lipopolysaccharide-induced in vitro desensitization by interferon-gamma. Eur J Immunol. 1990 May;20(5):1181–1184. doi: 10.1002/eji.1830200535. [DOI] [PubMed] [Google Scholar]
  17. Karima R., Matsumoto S., Higashi H., Matsushima K. The molecular pathogenesis of endotoxic shock and organ failure. Mol Med Today. 1999 Mar;5(3):123–132. doi: 10.1016/s1357-4310(98)01430-0. [DOI] [PubMed] [Google Scholar]
  18. Labeta M. O., Durieux J. J., Spagnoli G., Fernandez N., Wijdenes J., Herrmann R. CD14 and tolerance to lipopolysaccharide: biochemical and functional analysis. Immunology. 1993 Nov;80(3):415–423. [PMC free article] [PubMed] [Google Scholar]
  19. LeMay L. G., Otterness I. G., Vander A. J., Kluger M. J. In vivo evidence that the rise in plasma IL 6 following injection of a fever-inducing dose of LPS is mediated by IL 1 beta. Cytokine. 1990 May;2(3):199–204. doi: 10.1016/1043-4666(90)90016-m. [DOI] [PubMed] [Google Scholar]
  20. Lepe-Zuniga J. L., Klostergaard J. Tolerance to endotoxin in vitro: independent regulation of interleukin-1, tumor necrosis factor and interferon alpha production during in vitro differentiation of human monocytes. Lymphokine Res. 1990 Fall;9(3):309–319. [PubMed] [Google Scholar]
  21. Leung K. P., Russell S. W., LeBlanc P. A., Caballero S. Heterogeneity among macrophages cultured from mouse bone marrow. Morphologic, cytochemical and flow cytometric analyses. Cell Tissue Res. 1985;239(3):693–701. doi: 10.1007/BF00219251. [DOI] [PubMed] [Google Scholar]
  22. Li M. H., Seatter S. C., Manthei R., Bubrick M., West M. A. Macrophage endotoxin tolerance: effect of TNF or endotoxin pretreatment. J Surg Res. 1994 Jul;57(1):85–92. doi: 10.1006/jsre.1994.1115. [DOI] [PubMed] [Google Scholar]
  23. Lorsbach R. B., Russell S. W. A specific sequence of stimulation is required to induce synthesis of the antimicrobial molecule nitric oxide by mouse macrophages. Infect Immun. 1992 May;60(5):2133–2135. doi: 10.1128/iai.60.5.2133-2135.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Losman J. A., Chen X. P., Hilton D., Rothman P. Cutting edge: SOCS-1 is a potent inhibitor of IL-4 signal transduction. J Immunol. 1999 Apr 1;162(7):3770–3774. [PMC free article] [PubMed] [Google Scholar]
  25. Morrison D. C., Ryan J. L. Endotoxins and disease mechanisms. Annu Rev Med. 1987;38:417–432. doi: 10.1146/annurev.me.38.020187.002221. [DOI] [PubMed] [Google Scholar]
  26. Nicholson S. E., Hilton D. J. The SOCS proteins: a new family of negative regulators of signal transduction. J Leukoc Biol. 1998 Jun;63(6):665–668. doi: 10.1002/jlb.63.6.665. [DOI] [PubMed] [Google Scholar]
  27. Nose M., Uzawa A., Nomura M., Ikarashi Y., Nakata Y., Akashi M., Suzuki G. Control of endotoxin shock by the dried preparation of low virulent Streptococcus pyogenes OK-432. Cell Immunol. 1998 Sep 15;188(2):97–104. doi: 10.1006/cimm.1998.1357. [DOI] [PubMed] [Google Scholar]
  28. Pace J. L., MacKay R. J., Hayes M. P. Suppressive effect of interferon-beta on development of tumoricidal activity in mouse macrophages. J Leukoc Biol. 1987 Mar;41(3):257–263. doi: 10.1002/jlb.41.3.257. [DOI] [PubMed] [Google Scholar]
  29. Randow F., Syrbe U., Meisel C., Krausch D., Zuckermann H., Platzer C., Volk H. D. Mechanism of endotoxin desensitization: involvement of interleukin 10 and transforming growth factor beta. J Exp Med. 1995 May 1;181(5):1887–1892. doi: 10.1084/jem.181.5.1887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Severn A., Xu D., Doyle J., Leal L. M., O'Donnell C. A., Brett S. J., Moss D. W., Liew F. Y. Pre-exposure of murine macrophages to lipopolysaccharide inhibits the induction of nitric oxide synthase and reduces leishmanicidal activity. Eur J Immunol. 1993 Jul;23(7):1711–1714. doi: 10.1002/eji.1830230747. [DOI] [PubMed] [Google Scholar]
  31. Song M. M., Shuai K. The suppressor of cytokine signaling (SOCS) 1 and SOCS3 but not SOCS2 proteins inhibit interferon-mediated antiviral and antiproliferative activities. J Biol Chem. 1998 Dec 25;273(52):35056–35062. doi: 10.1074/jbc.273.52.35056. [DOI] [PubMed] [Google Scholar]
  32. Starr R., Willson T. A., Viney E. M., Murray L. J., Rayner J. R., Jenkins B. J., Gonda T. J., Alexander W. S., Metcalf D., Nicola N. A. A family of cytokine-inducible inhibitors of signalling. Nature. 1997 Jun 26;387(6636):917–921. doi: 10.1038/43206. [DOI] [PubMed] [Google Scholar]
  33. Stoiber D., Kovarik P., Cohney S., Johnston J. A., Steinlein P., Decker T. Lipopolysaccharide induces in macrophages the synthesis of the suppressor of cytokine signaling 3 and suppresses signal transduction in response to the activating factor IFN-gamma. J Immunol. 1999 Sep 1;163(5):2640–2647. [PubMed] [Google Scholar]
  34. Tracey K. J., Fong Y., Hesse D. G., Manogue K. R., Lee A. T., Kuo G. C., Lowry S. F., Cerami A. Anti-cachectin/TNF monoclonal antibodies prevent septic shock during lethal bacteraemia. Nature. 1987 Dec 17;330(6149):662–664. doi: 10.1038/330662a0. [DOI] [PubMed] [Google Scholar]
  35. Virca G. D., Kim S. Y., Glaser K. B., Ulevitch R. J. Lipopolysaccharide induces hyporesponsiveness to its own action in RAW 264.7 cells. J Biol Chem. 1989 Dec 25;264(36):21951–21956. [PubMed] [Google Scholar]
  36. Zhang X., Alley E. W., Russell S. W., Morrison D. C. Necessity and sufficiency of beta interferon for nitric oxide production in mouse peritoneal macrophages. Infect Immun. 1994 Jan;62(1):33–40. doi: 10.1128/iai.62.1.33-40.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

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