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Signal transduction mechanism by which lipopolysaccharides from various periodontopathic bacteria induce murine B lymphocyte activation

Research Project

Project/Area Number 09671851
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Morphological basic dentistry
Research InstitutionIwate Medical University (1998)
Osaka University (1997)

Principal Investigator

KIMURA Shigenobu  Iwate Medical University School of Dentistry, Department of Oral Microbiology, Professor, 歯学部, 教授 (10177917)

Co-Investigator(Kenkyū-buntansha) HAMADA Shigeyuki  Osaka University Faculty of Dentistry, Department of Oral Microbiology Professor (60028777)
KAWABATA Shigetada  Osaka University Faculty of Dentistry, Department of Oral Microbiology Associate (50273694)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1998: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1997: ¥2,100,000 (Direct Cost: ¥2,100,000)
Keywordsperiodontopathic bacteria / LPS / mouse / Blymphocytes / signal transduction / tyrosine phosphorylation / proliferative response
Research Abstract

In this study using the Iipopolysaccharides (LPS) from Porphyronwnas gingivalis as well as other periodontopathic bacteria including Prevotella intermedia, Actinobacillus actinomycetemcomitans and Eikenella corrodens (PgLPS, AaLPS, PiLPS and EiLPS, respectively), the nature of LPS-induced signal transduction mechanism that mediates later cellular responses of Blymphocytes was examined. When detected under Western blot analysis by using the monoclonal anti-phosphotyrosine antibody, all the LPSs as well as Escherichia coli LPS (EcLPS) induced tyrosine phosphorylation in the B lymphocytes from LPS-responsive C3H/HeN mice. In the LPS-hyporesponsive C3H/HeJ B lymphocytes, however, the trigger signals could be induced by PgLPS and PiLPS, but not by AaLPS or EiLPS.Furtherrnore, lipid A from Salmonella minnesota also induced tyrosine phosphorylation in C3H/HeN B lymphocytes. It was reported that the lipid A moieties of PgLPS and PiLPS were quite different from those of EcLPS, AaLPS or EiLPS.Th … More us, these results si.iggest that lipid A moiety of LPS could be potent for the LPS-induced tyrosine phosphoxylation in B lymphocytes. The treatment with tyrosine kinase inhibitors, herbimycin A and Lenistein, abrogated the LPS-induced tyrosine phosphorylation and the proliferative response, suggesting that LPS-induced tyrosine phosphorylation could be an important signaling event that might lead to cellular responses. However, no obvious effect has been observed by the treatment with a phosphatase inhibitor (phenylarsine oxide). In addition, increased serine threonine protein phosphorylation in B lymphocytes could be also important, since the proliferative response following LPS stimulation was inhibited by the preincubation with a serine threonine kinase inhibitor, staurosponne. Taken together, the present findings suggest that the pen odontopathic bacteria have a potent property to induce the stimulation of B lymphocytes by the lipid A moiety, in which increased tyrosine phosphorylation folJowed by other protein phosphorylations could be important signaling events that might lead to cellular responses. Less

Report

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

    (8 results)

All Other

All Publications (8 results)

  • [Publications] 古賀俊也: "歯周病原性細菌のLPS刺激によるB細胞内チロシンリン酸化反応" 歯基礎誌. 39巻. 493 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 木村重信: "細菌菌体成分によるマウス由来株化B細胞CH12LXのCD14依存性/非依存性活性化" 日本細菌学雑誌. 53巻. 135 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 木村重信: "P.gingivalisのLPS刺激によるマウスB細胞内シグナル伝達機構" 歯基礎誌. 40巻. 424 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Toshiya Koga et al.: "Signal transduction mechanism by which lipopolysaccharides from various periodontopathic bacteria induce murine B lymphocyte activation.Japan" J.Oral.Biol.39. 493 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Shigenobu Kimura et al.: "CD14-Dependent and Independent Pathways in Lipopolysaccharides-induced Activation of a Murine B Cell Line, CH12.LX.Japan." J.Bacteriol.53. 135 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Shigenobu Kimura et al.: "Signal transduction mechanism in murine B lymphocytes by stimulation with ipopolysaccharide from Porphyromonas gingivalis.Japan" J.Oral.Biol.40. 424 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 木村重信: "細菌菌体成分によるマウス由来株化B細胞CH12.LXのCD14依存性/非依存性活性化" 日本細菌学雑誌. 53巻. 135 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 木村重信: "P.gingivalisのLPS刺激によるマウスB細胞内シグナル伝達機構" 歯基礎誌. 40巻. 424 (1998)

    • Related Report
      1998 Annual Research Report

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

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