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Activation of human gingival epithelial cells by black-pigmented bacteria

Research Project

Project/Area Number 09671843
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Morphological basic dentistry
Research InstitutionTohoku University

Principal Investigator

SUGAWARA Shunji  School of Dentistry, Tohoku University, Assistant Professor, 歯学部, 助手 (10241639)

Co-Investigator(Kenkyū-buntansha) SUGIYAMA Akiko  School of Dentistry, Tohoku University, JSPS Fellow, 歯学部, 日本学術振興会特別研
RIKIISHI Hidemi  School of Dentistry, Tohoku University, Lecturer, 歯学部, 講師 (70091767)
TAKADA Haruhiko  School of Dentistry, Tohoku University, Professor, 歯学部, 教授 (30135743)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1998: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1997: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsblack-pigmented bacteria / human gingival epithelial cells / cytokines / adhesion molecules / activation mechanism
Research Abstract

1. Human gingival epithelial cells produce interleukin (IL)-8, granulocyte-colony stimulating factor and granulocyte-macrophage colony stimulating factor in response to Prevotella intermedia glycoprotein (PGP), and fimbriae andl ipopolysaccharide (LPS) fraction of Porphyromonas gingivalis. In contrast, the cells produce macrophage-colony stimulating factor stimulated with interferon (IFN)-gamma.
2. P.intermedia PGP, fimbriae and LPS fraction of P.gingivalis augmented the expression of intercellular adhesionmolecule-1 (ICAM-1) on the surface of human gingival epithelial cells, flow cytometically.
3. mRNA induction of the above cytokines and ICAM-1 in the cells by the components of black-pigmented bacteria (BPB)was confirmed by reverse-transcriptase PCR.
4. Human gingival epithelial cells do not express CD14, a major LPS receptor, which indicates that the cells are activated by the components of BPB with a distinct pathway from LPS of Enterobacteriaceae. In 1998, Toll-like receptors (TLRs)were reported to be signaling molecules of UPS, and also TLRs mediated LPS signal in a CD14-independent manner at a high concentration of LPS.The experiment that TLRs participate in the activation of human gingival epithelial cells by components of BPB is under way.
5. Human gingivalepithelial cells possess IL-18, a IFN-gamma inducing factor, in the cells as a possibly precursor form. Thes timulants used in this study could not induce the secretion of IL-18 by the cells. However, it is possible that IL-18produced by the cells with some stimulation, such as apoptotic pathway may induce IFN-gamma by immune cells, and that in turn, IFN-gamma produced may participate in the onset and cure of inflammation in periodontium.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] 菅原 俊二: "菌体表層成分と歯周病 試論 : 歯周組織におけるCD14分子の役割" 歯科基礎医学会雑誌. 40・1. 1-16 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sugawara, S.: "Heterogeneous expression and release of CD14 by human gingival fibroblasts : Characterization CD14-mediated interleukin-8 secretion in response to lipopolysaccharide." Infection and Immunity. 66・7. 3043-3049 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Arakaki, R.: "A lipoteichoic acid fraction of Enterococcus hirae activates cultured human monocytic cells via a CD14-independent pathway to promote cytokine production, and the activity is inhibited by serum components." FEMS Immunology and Medical Microbiology. 22・4. 283-291 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sugawara, S.: "Bacteria cell surface components and periodontal disease-possible roles of CD14 molecules in periodontal tissues-." Japanese Journal of Oral Biology. 40-1. 1-6 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sugawara, S.: "Heterogeneous expression and release of CD14 by human gingival fibroblasts : Characterization CD14-mediated interleukin-8 secretion in response to lipopolysaccharide." Infection and Immunity. 66-7. 3043-3049 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Arakaki, R.: "A lipoteichoic acid fraction of Enterococus hirae activates cultured human monocytic cells via a CD14-independent pathway to promote cytokine production, and the activity is inhibited by serum components" FEMS Immunology and Medical Microbiology. 22-4. 283-291 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sugawara,S.: "Heterogeneous expression and release of CD14 by human gingival fibroblasts : Characterization CD14-mediated interleukin-8 secretion in response to lipopolysaccharide." Infection and Immunity. 66・7. 3043-3049 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Arakaki,R.: "A lipoteichoic acid fraction of Enterococcus hirae activates cultured human monocytic cells via a CD14-independent pathway to promote cytokine production, and the activity is inhibited by serum components." FEMS Immunology and Medical Microbiology. 22・4. 283-291 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 菅原俊二: "菌体表層成分と歯周病試論 : 歯周組織におけるCD14分子の役割" 歯科基礎医学会雑誌. 40・1. 1-16 (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] Liu,Z.X.: "Accessory cell function of a human colonic epithelial cell line HT-29 for bacterial superantigens." Climical Experimental Immunology. 108・3. 384-391 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Rikiishi,H.: "Superantigenicity of helper T-cell mitogen (SPM-2) isolated from culture supernatants of Streptococcus pyogenes." Immunology. 91・3. 406-413 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Horiuchi,N.: "Pripheral blood lymphocytes from psoriatic patients are hyporesponsive to β-strptococcal supernatigens." Britishi Journal of Dermatology. 137・6(印刷中). (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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