Display options
Share it on

Mediators Inflamm. 1996;5(1):56-61. doi: 10.1155/S0962935196000105.

Adhesion-independent synergy of monocytes and endothelial cells in cytokine production: regulation of IL-6 and GM-CSF production by PAF.

Mediators of inflammation

C Lacasse, S Turcotte, D Gingras, M Rola-Pleszczynski

Affiliations

  1. Immunology Division Department of Pediatrics Faculty of Medicine Université de Sherbrooke Sherbrooke QC Canada.

PMID: 18475699 PMCID: PMC2365774 DOI: 10.1155/S0962935196000105

Abstract

Co-Cultures of monocytes (MO) and endothelial cells (EC) were studied for their capacity to synergize in the production of interleukin-6 (IL-6) and granulocyte-macrophage colony-stimulating factor (GM-CSF), two cytokines potentially important in vascular physiopathology. Resting monocytes produced detectable amounts of IL-6 but no GM-CSF, whereas confluent EC produced significant quantities of GM-CSF, but minimal IL-6. In co-cultures without stimuli, additive synthesis of both cytokines was observed. When EC were pretreated, however, with either PAF, TNF or both stimuli, before addition of MO, synergistic production of IL-6 was observed. In contrast, GM-CSF production was not enhanced by coculture of monocytes with activated EC. When either cell population was fixed with paraformaldehyde or killed by freeze-thawing before addition to the co-culture, cytokine levels reverted to those produced by the unaffected population alone. On the other hand, separating the two cell populations by a cell-impermeable membrane in transwell cultures did not affect the synergistic production of the cytokines. Taken together, our data suggest that EC and MO can synergize in response to stimuli by producing IL-6 and that this synergy is dependent on the integrity of both cell populations, but independent of cell-cell contact.

References

  1. Science. 1988 Jan 29;239(4839):502-4 - PubMed
  2. J Clin Invest. 1986 Nov;78(5):1316-23 - PubMed
  3. J Immunol. 1992 Dec 1;149(11):3682-8 - PubMed
  4. J Lipid Mediat. 1993 Mar-Apr;6(1-3):175-81 - PubMed
  5. Curr Top Microbiol Immunol. 1986;132:105-13 - PubMed
  6. Nature. 1986 Sep 4-10;323(6083):79-82 - PubMed
  7. J Immunol. 1989 Jun 15;142(12):4339-45 - PubMed
  8. Nature. 1989 May 11;339(6220):150-2 - PubMed
  9. J Exp Med. 1972 Dec 1;136(6):1356-77 - PubMed
  10. Proc Natl Acad Sci U S A. 1982 May;79(9):2768-72 - PubMed
  11. Proc Natl Acad Sci U S A. 1986 Jan;83(2):446-50 - PubMed
  12. J Clin Invest. 1977 Aug;60(2):449-54 - PubMed
  13. Blood. 1988 Oct;72(4):1134-40 - PubMed
  14. Biochem Biophys Res Commun. 1987 Feb 13;142(3):754-60 - PubMed
  15. J Biol Chem. 1979 Oct 10;254(19):9355-8 - PubMed
  16. Proc Natl Acad Sci U S A. 1984 Aug;81(15):4917-21 - PubMed
  17. Cell Immunol. 1989 Sep;122(2):493-503 - PubMed
  18. Immunology. 1981 Feb;42(2):191-9 - PubMed
  19. Immunol Lett. 1993 Feb;35(2):109-17 - PubMed
  20. J Biol Chem. 1990 Oct 15;265(29):17381-4 - PubMed
  21. J Clin Invest. 1973 Nov;52(11):2745-56 - PubMed
  22. Eur J Immunol. 1987 Oct;17(10):1411-6 - PubMed
  23. J Clin Invest. 1986 Aug;78(2):587-91 - PubMed
  24. Blood. 1985 Mar;65(3):513-25 - PubMed
  25. J Clin Invest. 1987 Jan;79(1):48-51 - PubMed
  26. Semin Thromb Hemost. 1987 Oct;13(4):445-53 - PubMed
  27. Immunology. 1991 Feb;72(2):181-7 - PubMed
  28. Cell. 1987 Feb 27;48(4):671-9 - PubMed
  29. J Immunol. 1989 Jan 1;142(1):144-7 - PubMed
  30. Nature. 1974 Apr 19;248(5450):703-4 - PubMed
  31. Proc Natl Acad Sci U S A. 1989 Sep;86(18):7169-73 - PubMed
  32. Proc Natl Acad Sci U S A. 1986 Oct;83(19):7467-71 - PubMed

Publication Types