Skip to main content
Log in

Gram-Negative, but Not Gram-Positive, Bacteria Elicit Strong PGE2 Production in Human Monocytes

  • Published:
Inflammation Aims and scope Submit manuscript

Abstract

Gram-positive and Gram-negative bacteria induce different cytokine patterns in human mononuclear cells. We have seen that Gram-positives preferentially induce IL-12 and TNF-α, whereas Gram-negatives induce more IL-10, IL-6, and IL-8. In this study, we compared the capacity of these two groups of bacteria to induce PGE2. Monocytes stimulated with Gram-negative bacterial species induced much more PGE2 than did Gram-positive bacteria (5600 ± 330 vs. 1700 ± 670 pg/mL, p<;0.001). Blocking of COX-2 by NS398 abolished PGE2 production, but did not alter the cytokine patterns induced by Gram-positive and Gram-negative bacteria. We suggest that Gram-positive and Gram-negative bacteria may stimulate different innate effector functions; Gram-positive bacteria promoting cell-mediated effector functions whereas Gram-negative bacteria inducing mediators inhibiting the same.

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. Williams, T. J. and J. Morely. 1973. Prostaglandins as potentiators of increased vascular permeability in inflammation. Nature 246:215–217.

    Google Scholar 

  2. Milton, A. S. and S. Wendlandt. 1971. Effects on body temperature of prostaglandins of the A, E and F series on injection into the third ventricle of unanaesthetized cats and rabits. J. Physiol. 218:325–336.

    Google Scholar 

  3. Ferreira, S. H., M. de Abreu Nakamura, and M. S. Castro. 1978. The hyperalgesic effects of prostacyclin and prostaglandin E2. Prostaglandins 16:31–37.

    Google Scholar 

  4. Di Battista, J. A., J. Martel-Pelletier, and J. Pelletier 1999. Suppression of tumor necrosis factor (TNF-alpha) gene expression by prostaglandin E(2). Role Of early growth response protein-1 (Egr-1). Osteoarthritis Cartilage 7:395–398.

    Google Scholar 

  5. Aloisi, F., R. De Simone, S. Columba-Cabezas, and G. Levi. 1999. Opposite effects of interferon-gamma and prostaglandin E2 on tumor necrosis factor and interleukin-10 production in microglia: A regulatory loop controlling microglia pro-and anti-inflammatory activities. J. Neurosci. Res. 56:571–580.

    Google Scholar 

  6. van der Pouw Kraan, T. C., L. C. Boeije, R. J. Smeenk, J. Wijdenes, and L. A. Aarden. 1995. Prostaglandin-E2 is a potent inhibitor of human interleukin 12 production. J. Exp. Med. 181:775–779.

    Google Scholar 

  7. Wu, C. Y., K. Wang, J. F. McDyer, and R. A. Seder. 1998. Prostaglandin E2 and dexamethasone inhibit IL-12 receptor expression and IL-12 responsiveness. J. Immunol. 161:2723–2730.

    Google Scholar 

  8. Demeure, C. E., L. P. Yang, C. Desjardins, P. Rynauld, and G. Delespesse. 1997. Prostaglandin E2 primes naive T cells for the production of anti-inflammatory cytokins. Eur. J. Immunol. 27:3526–3531.

    Google Scholar 

  9. Katamura, K., N. Shintaku, Y. Yamauchi, T. Fukui, Y. Ohshima, M. Mayumi, and K. Furusho. 1995. Prostaglandin E2 at priming of naive CD4+ T cells inhibits acquisition of ability to produce IFN-gamma and IL-2, but not IL-4 and IL-5. J. Immunol. 155:4604–4612.

    Google Scholar 

  10. Snijdewint, F. G., P. Kalinski, E. A. Wiernga, J. D. Bos, and M. L. Kapsenberg. 1993. Prostaglandin E2 differentially modulates cytokine secretion profiles of human T helper lymphocytes. J. Immunol. 150:5321–5329.

    Google Scholar 

  11. Hessle, C., B. Andersson, and A. E. Wold. 2000. Gram-positive bacteria are potent inducers of monocytic interleukin-12 (IL-12) while gram-negative bacteria preferentially stimulate IL-10 production. Infect. Immun. 68:3581–3586.

    Google Scholar 

  12. Baddiley, J. 1989. Bacterial cell wall and membranes. Discovery of the teichoic acids. Bioessays 10:207–210.

    Google Scholar 

  13. Fischer, W. 1989. Bacterial Phosphoglycolipids and Lipotheichoic Acids. Plenum, NY.

    Google Scholar 

  14. Galanos, C., O. Luderitz, and O. Westphal. 1969. A new method for the extraction of R lipopolysaccharides. Eur. J. Biochem. 9:245–249.

    Google Scholar 

  15. Mattsby Baltzer, I., K. Lindgren, B. Lindholm, and L. Edebo. 1991. Endotoxin shedding by enterobacteria: Free and cell-bound endotoxin differ in Limulus activity. Infect. Immun. 59:689–695.

    Google Scholar 

  16. Nau, G. J., J. F. L. Richmond, A. Schlesinger, E. G. Jennings, E. S. Lander, and R. A. Young. 2002. Human macrophage activation programs induced by bacterial pathogens. Proc. Natl. Acad. Sci. U. S. A. 99:1503–1508.

    Google Scholar 

  17. Havell, E. A. 1992. Role of TNF in resistance to bacteria. Immunol. Ser. 56:341–363.

    Google Scholar 

  18. Cross, A. S., S. M. Opal, J. C. Sadoff, and P. Gemski. 1993. Choice of bacteria in animal models of sepsis. Infect. Immun. 61:2741–2747.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Christina C. Hessle.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hessle, C.C., Andersson, B. & Wold, A.E. Gram-Negative, but Not Gram-Positive, Bacteria Elicit Strong PGE2 Production in Human Monocytes. Inflammation 27, 329–332 (2003). https://doi.org/10.1023/B:IFLA.0000006700.41614.21

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:IFLA.0000006700.41614.21

Navigation