Porphyromonas gingivalis의 각종 표면성분이 싸이토카인 형성에 미치는 영향

The cytokine-inducing activities of surface components of the periodontopathogenic bacterium Porphyromonas gingivalis

  • 김성조 (부산대학교 치과대학 치주과학교실)
  • Kim, Sung-Jo (Department of Periodontology, College of Dentistry, Pusan National University)
  • 발행 : 2005.09.30

초록

This study was carried out to examine the potency of the three surface compo- nents from Porphyromonas gingivalis to stimulate the murine macrophage cell line RAW264.7 to synthesize the pro-inflammatory cytokine tumor necrosis factor alpha($TNF-{\alpha}$) and nitric oxide (NO). Lipopolysaccharide(LPS). lipid A-associated proteins(LAP) and saline-extractable surface -associated material(SAM) were isolated from P. gingivalis 381. $TNF-{\alpha}$ release into culture supernatants was determined by two-site ELISA. NO production was assayed by measuring the accumulation of nitrite in culture supernatants. Western blot analysis of iNOS and analysis of reverse transcription(RT)-PCR products were carried out. The surface components extracted from this bacterium were almost equally potent in stimulating release of $TNF-{\alpha}$ and NO by RAW264.7 cells. $TNF-{\alpha}$ that was being measured immunologically was due to activation of $TNF-{\alpha}$ gene transcription. The present study clearly shows that P. gingivalis surface components fully induced iNOS expression in RAW264.7 cells in the absence of other stimuli. The ability of P. gingivalis surface components to promote the production of $TNF-{\alpha}$ and NO may be important in the pathogenesis of inflammatory periodontal disease.

키워드

참고문헌

  1. Slots J, Listgarten MA. Bacteroides gingivalis, Bacteroides intermedius and Actinobacillus actinomycetemcomitans in human periodontal diseases. J Clin Periodontol 1988: 15:85-93 https://doi.org/10.1111/j.1600-051X.1988.tb00999.x
  2. Wilson M. Biological activities of lipopolysaccharide and endotoxin. In Shah HN, Mayrand D, Genco RJ(eds) Biology of the species Porphyromones gingivalis. CDC Press pp 171-198, 1993
  3. Hitchcock PJ, Morrison DC. The protein components of bacterial endotoxins. In Rietchel ET (ed) Handbook of Endotoxins, vol 1: Chemistry of Endotoxin. Elsevier: North Holland, pp 339-375, 1984
  4. Porat R, Yanoov M. Johns MA, Shibolet S, Michalevicz R, Effects of endotoxinassociated protein on hematopoiesis. Infect Immun 1992:60:1756-1760
  5. Wilson M. Meghji S, Barber P, Henderson B, Biological activities of surface-associated material from Porphyromonas gingivalis. FEMS Immunol Med Microbiol 1993:6: 147-156 https://doi.org/10.1111/j.1574-695X.1993.tb00317.x
  6. Reddi K, Wilson M, Nair S, Poole S, Henderson B, Comparison of the pro-inflammatory cytokine-stimulating activity of the surface-associated proteins of periodontopathic bacteria. J Periodont Res 1996:31: 120-130 https://doi.org/10.1111/j.1600-0765.1996.tb00473.x
  7. Reddi K, Wilson M. Poole S, Meghji S, Henderson B. Relative cytokine-stimulating activities of surface components of the oral periodontopathogenic bacterium Actinobacillus actinomycetemcomitans. Cytokine 1995: 7: 534-541 https://doi.org/10.1006/cyto.1995.0072
  8. Meghji S, Henderson B, Kirby A Newman HN. Wilson M. Serum antibody response to surface-associated material from periodontopathogenic bacteria. FEMS Immunol Med Microbiol 1995:10:101-108 https://doi.org/10.1111/j.1574-695X.1995.tb00017.x
  9. Herminajeng E. Asmara W. Yuswanto A, Barid I, Sosroseno W. Protective humoral immunity induced by surface-associated material from Actinobacillus ectinomycetemcomitans in mice. Microbes Infect 2001:3 :997-1003 https://doi.org/10.1016/S1286-4579(01)01463-0
  10. Meghji S, Wilson M. Henderson B, Kinane D. Anti-proliferative and Cytotoxic activity of surface-associated material from periodontopathogenic bacteria. Arch Oral Biol 1992:37:637-644 https://doi.org/10.1016/0003-9969(92)90126-S
  11. Meghji S, Henderson B, Nair S, Wilson M. Inhibition of bone DNA and collagen production by surface-associated material from bacteria implicated in the pathology of periodontal diseases. J Periodontol 1992: 63: 736-742 https://doi.org/10.1902/jop.1992.63.9.736
  12. Meghji S, Wilson M. Barber P, Henderson B. Bone resorbing activity of surface-associated material from Actinobacillus ectinomycetemcomitans and Eikenella corrodens. J Med Microbiol 1994:41: 197-203 https://doi.org/10.1099/00222615-41-3-197
  13. Bjornson BH. Agura E, Harvey J et al. Endotoxin-associated protein: a potent stimulus for human granulopoietic activity which may be accessory cell independent. Infect Immun 1988: 56: 1602-1607
  14. Sultzer BM. Genetic factors in leukocyte responses to endotoxin: further studies in mice. J Immunol 1969:103:32-38
  15. Sultzer BM, Goodman GW. Endotoxin protein: a B cell mitogen and polyclonal activator of C3H/HeJ lymphocytes. J Exp Med 1976: 144:821-827 https://doi.org/10.1084/jem.144.3.821
  16. Reddi K, Poole S, Nair S et al. Lipid A-associated proteins from periodontopathogenic bacteria induce interleukin-6 production by human gingival fibroblasts and monocytes. FEMS Immunol Med Microbiol 1995:11:137-144 https://doi.org/10.1111/j.1574-695X.1995.tb00100.x
  17. Sharp L, Poole S, Reddi K et al. A lipid A-associated protein of Porphyromones gjngjvalis, derived from the haemagglutinating domain of the RI protease gene family, is a potent stimulator of interleukin 6 synthesis. Microbiology 1998: 144: 3019-3026 https://doi.org/10.1099/00221287-144-11-3019
  18. Reddi K, Meghji S, Wilson M. Henderson B. Comparison of the osteolytic activity of surface-associated proteins of bacteria implicated in periodontal disease. Oral Dis 1995: 1: 26-31 https://doi.org/10.1111/j.1601-0825.1995.tb00153.x
  19. Wilson M, Kamin S, Harvey W. Bone resorbing activity of purified capsular material from Actinobacillus actinomycetemcomitans, J Periodont Res 1985:20: 484-491 https://doi.org/10.1111/j.1600-0765.1985.tb00831.x
  20. Morrison DC, Leive L. Fractions of lipo-polysaccharides from E. coli 0111: B4 prepared by two extraction procedures. J Biol Chem 1975:250:2911-2919
  21. Westphal O, Jann K. (1965) Bacterial lipopolysaccharides: extraction with phenol-water and further applications of the procedure. In: RL Whistler eds. Methods in carbohydrate chemistry. New York: Academic Press, 83-91
  22. Green LC, Wagner DA, Glogowski J et al. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids. Anal Biochem 1982;126:131-138. https://doi.org/10.1016/0003-2697(82)90118-X
  23. Honig J. Rordorf-Adam C. Siegmund C. Wiedemann W. Erard F. Increased interleukin-1 beta concentration in gingival tissue from periodontitis patients. J Periodont Res 1989:24:362-367 https://doi.org/10.1111/j.1600-0765.1989.tb00883.x
  24. Stashenko P. Jandinski JJ. Fujiyioshi P, Rynar J. Socranski SS. Tissue levels of bone resorptive cytokines in periodontal disease. J Periodontol 1991:62:504-509 https://doi.org/10.1902/jop.1991.62.8.504
  25. Moncada S. Palmer RMJ. Higgs EA. Nitric oxide: physiology. pathology. and pharmacology. Pharmacol Rev 1991 :43: 109-142
  26. Nathan C. Xie QW. Nitric oxide synthases: roles. tolls and controls. Cell 1994:78 :915-918 https://doi.org/10.1016/0092-8674(94)90266-6
  27. Geller DA, Nussler AK. Di Silvio M et al. Cytokines, endotoxin, and glucocorticoids regulate the expression of inducible nitric oxide synthase in hepatocytes. Proc Natl Acad Sci USA 1993:90:522-526 https://doi.org/10.1073/pnas.90.2.522
  28. Nathan C. Xie QW. Regulation of biosynthesis of nitric oxide. J Biol Chem 1994: 269:13725-13728
  29. Southey A, Tanaka S. Murakami T et al. Pathophysiological role of nitric oxide in rat experimental colitis. Int J Immuno-pharmacol 1997: 19: 669-676
  30. Weinberg JB. Granger DL. Pisetsky DS et al. The role of nitric oxide in the pathogenesis of spontaneous murine autoimmune disease: increased nitric oxide production and nitric oxide synthase expression in MRL-1pr/1pr mice, and reduction of spontaneous glomerulonephritis and arthritis by orally administered NG-monomethyl-L-arginine. J Exp Med 1994: 179: 651-660 https://doi.org/10.1084/jem.179.2.651
  31. Matejka M, Partyka L, Ulm C, Solar P, Sinzinger H. Nitric oxide synthesis is increased in periodontal disease. J Periodont Res 1998:33:517-518 https://doi.org/10.1111/j.1600-0765.1998.tb02352.x
  32. Blix IJ, Helgeland K. LPS from Actinobacillus actinomycetemcomitansand production of nitric oxide in murine macrophages J774. Eur J Oral Sci 1998: 106: 576-581 https://doi.org/10.1046/j.0909-8836.1998.eos106107.x
  33. Sosroseno W. Barid I, Herminajeng E, Susilowati R. Nitric oxide production by a murine macrophage cell line (RAW264.7) stimulated with lipopolysaccharide from Actinobacillus actinomycetemcomitans. Oral Microbiol Immunol 2002: 17:72-78 https://doi.org/10.1046/j.0902-0055.2001.00091.x
  34. Kim SJ, Ha MS, Choi EY, Choi JI, Choi IS. Prevotella intermedia lipopolysaccharide stimulates release of nitric oxide by inducing expression of inducible nitric oxide synthase. J Periodont Res 2004: 39:424-431 https://doi.org/10.1111/j.1600-0765.2004.00757.x
  35. Kim SJ, Ha MS, Choi EY, Choi JI, Choi IS. Nitric oxide production and inducible nitric oxide synthase expression induced by Prevotella nigrescens lipopolysaccharide. FEMS Immunol Med Microbiol 2005 :43: 51-58 https://doi.org/10.1016/j.femsim.2004.07.001
  36. Batista AC, Silva TA, Chun JH. Lara VS. Nitric oxide synthesis and severity of human periodontal disease. Oral Dis 2002 :8:254-260 https://doi.org/10.1034/j.1601-0825.2002.02852.x
  37. Hirose M, Ishihara K. Saito A et al. Expression of cytokines and inducible nitric oxide synthase in inflamed gingival tissue. J Periodontol 2001:72:590-597 https://doi.org/10.1902/jop.2001.72.5.590
  38. Kendall HK. Haase HR, Li H. Xiao Y. Bartold PM. Nitric oxide synthase type-II is synthesized by human gingival tissue and cultured human gingival fibroblasts. J Periodont Res 2000:35: 194-200 https://doi.org/10.1034/j.1600-0765.2000.035004194.x
  39. Lappin DF, Kjeldsen M. Sander L, Kinane DF. Inducible nitric oxide synthase expression in periodontitis. J Periodont Res 2000:35:369-373 https://doi.org/10.1034/j.1600-0765.2000.035006369.x