Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1992 Oct;60(10):4179–4183. doi: 10.1128/iai.60.10.4179-4183.1992

Induction of procoagulant activity on human endothelial cells by Streptococcus pneumoniae.

S Geelen 1, C Bhattacharyya 1, E Tuomanen 1
PMCID: PMC257450  PMID: 1398928

Abstract

The inflammatory response in infection caused by gram-negative organisms involves induction of procoagulant activity (PCA) on human endothelial cells. Although infections caused by gram-positive organisms are also associated with fibrin formation and thrombosis, the bacterial determinants inducing PCA are unknown. This study shows that intact pneumococci and the pneumococcal cell wall efficiently induce PCA on human endothelial cells. Upon exposure of endothelial cells to pneumococci, PCA was first detectable at 30 min, peaked at 2 h, and disappeared by 6 h. The specific activities of encapsulated and unencapsulated strains for induction of PCA were equivalent. Purified pneumococcal cell walls were as potent as endotoxin in induction of PCA. The ability to induce a procoagulant state on endothelial cells is a new biological activity of gram-positive cell walls which promotes the participation of the coagulation cascade in the inflammatory response to disease caused by gram-positive organisms.

Full text

PDF
4179

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bevilacqua M. P., Pober J. S., Majeau G. R., Fiers W., Cotran R. S., Gimbrone M. A., Jr Recombinant tumor necrosis factor induces procoagulant activity in cultured human vascular endothelium: characterization and comparison with the actions of interleukin 1. Proc Natl Acad Sci U S A. 1986 Jun;83(12):4533–4537. doi: 10.1073/pnas.83.12.4533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bisno A. L., Freeman J. C. The syndrome of asplenia, pneumococcal sepsis, and disseminated intravascular coagulation. Ann Intern Med. 1970 Mar;72(3):389–393. doi: 10.7326/0003-4819-72-3-389. [DOI] [PubMed] [Google Scholar]
  3. Cabellos C., MacIntyre D. E., Forrest M., Burroughs M., Prasad S., Tuomanen E. Differing roles for platelet-activating factor during inflammation of the lung and subarachnoid space. The special case of Streptococcus pneumoniae. J Clin Invest. 1992 Aug;90(2):612–618. doi: 10.1172/JCI115900. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chetty C., Kreger A. Generation of purpura-producing principle from pneumococcal cell walls. J Bacteriol. 1985 Jul;163(1):389–391. doi: 10.1128/jb.163.1.389-391.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Colucci M., Balconi G., Lorenzet R., Pietra A., Locati D., Donati M. B., Semeraro N. Cultured human endothelial cells generate tissue factor in response to endotoxin. J Clin Invest. 1983 Jun;71(6):1893–1896. doi: 10.1172/JCI110945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Nawroth P. P., Stern D. M., Kisiel W., Bach R. Cellular requirements for tissue factor generation by bovine aortic endothelial cells in culture. Thromb Res. 1985 Dec 1;40(5):677–691. doi: 10.1016/0049-3848(85)90305-6. [DOI] [PubMed] [Google Scholar]
  7. Nemerson Y., Bach R. Tissue factor revisited. Prog Hemost Thromb. 1982;6:237–261. [PubMed] [Google Scholar]
  8. Riesenfeld-Orn I., Wolpe S., Garcia-Bustos J. F., Hoffmann M. K., Tuomanen E. Production of interleukin-1 but not tumor necrosis factor by human monocytes stimulated with pneumococcal cell surface components. Infect Immun. 1989 Jul;57(7):1890–1893. doi: 10.1128/iai.57.7.1890-1893.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ripley-Petzoldt M. L., Giebink G. S., Juhn S. K., Aeppli D., Tomasz A., Tuomanen E. The contribution of pneumococcal cell wall to the pathogenesis of experimental otitis media. J Infect Dis. 1988 Feb;157(2):245–255. doi: 10.1093/infdis/157.2.245. [DOI] [PubMed] [Google Scholar]
  10. Rosenthal G. A., Levy G., Rotstein O. D. Induction of macrophage procoagulant activity by Bacteroides fragilis. Infect Immun. 1989 Feb;57(2):338–343. doi: 10.1128/iai.57.2.338-343.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Sinclair S. B., Rotstein O. D., Levy G. A. Disparate mechanisms of induction of procoagulant activity by live and inactivated bacteria and viruses. Infect Immun. 1990 Jun;58(6):1821–1827. doi: 10.1128/iai.58.6.1821-1827.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Stern D., Nawroth P., Handley D., Kisiel W. An endothelial cell-dependent pathway of coagulation. Proc Natl Acad Sci U S A. 1985 Apr;82(8):2523–2527. doi: 10.1073/pnas.82.8.2523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Tuomanen E., Baruch A. New antibodies as adjunctive therapies for Gram-positive bacterial meningitis. Pediatr Infect Dis J. 1989 Dec;8(12):923–928. doi: 10.1097/00006454-198912000-00047. [DOI] [PubMed] [Google Scholar]
  14. Tuomanen E., Liu H., Hengstler B., Zak O., Tomasz A. The induction of meningeal inflammation by components of the pneumococcal cell wall. J Infect Dis. 1985 May;151(5):859–868. doi: 10.1093/infdis/151.5.859. [DOI] [PubMed] [Google Scholar]
  15. Tuomanen E., Rich R., Zak O. Induction of pulmonary inflammation by components of the pneumococcal cell surface. Am Rev Respir Dis. 1987 Apr;135(4):869–874. doi: 10.1164/arrd.1987.135.4.869. [DOI] [PubMed] [Google Scholar]
  16. Tuomanen E., Tomasz A., Hengstler B., Zak O. The relative role of bacterial cell wall and capsule in the induction of inflammation in pneumococcal meningitis. J Infect Dis. 1985 Mar;151(3):535–540. doi: 10.1093/infdis/151.3.535. [DOI] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES