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2003 Fiscal Year Final Research Report Summary

Functional analysis of neutrophils that infiltrated in the S.mansoni-induced hepatic granuloma

Research Project

Project/Area Number 14570211
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 寄生虫学(含医用動物学)
Research InstitutionYamagata University

Principal Investigator

ASAO Hironobu  Yamagata University, Fuculty of Medicine, Professor, 医学部, 教授 (80250744)

Project Period (FY) 2002 – 2003
KeywordsS.Mansoni / neutrophil / hepatic granuloma / TNF-α
Research Abstract

Schistosomiasis mansoni is a chronic disease progressed after S.mansoni infection. S.mansoni is parasitic in the portal vein. The eggs produced by adult worms are embolized in the hepatic capillary blood vessels and then they form hepatic granulomas. Furthermore it progresses to liver cirrhosis finally. Neutrophils are supposed to have an important role for the hepatic granuloma formation. Then we employed mouse animal model of S.mansoni infection and neutrophil eliminating antibody to examine the functional role of neutrophil on the granuloma formation. 60 cercarias were infected in BALB/c mice intraperitoneally. Before infection or 7 weeks after infection just before egg production from adult worms, mice were injected with rat monoclonal antibody (RB6-8C5) to eliminate neutrophils. 8 or 9 weeks after infection, mouse liver was examined for histophathological examination and TNF-α production or the number of adult worms and eggs in infected mouse feces were checked. Though RB6-8C5 injections reduced the number of peripheral neutrophils dramatically but transiently, the size of formed hepatic granuloma, cells infiltrated in the granuloma, TNF-α production and the number of adult worms and eggs in the feces were not affected in the neutrophil eliminated mice as compared with control antibody injected mice. The transient elimination of neutrophils may not be sufficient to affect the granuloma formation and S.mansoni growth. We need further examinations with different doses and durations of antibody injection to remove neutrophil more completely.

  • Research Products

    (9 results)

All Other

All Publications (9 results)

  • [Publications] Morita E: "Human parvovirus B19 non-structural protein (NS1) induces cell cycle arrest at G1 phase."J.Virol.. 77. 2915-2921 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kikuchi K: "Identification of AMSH-LP containing a Jab1/MPN domain metalloenzyme motif."Biochem.Biophys.Res.Commun.. 306. 637-643 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kanazawa C: "Effects of deficiencies of STAMs and Hrs, mammalian class E Vps proteins, on receptor downregulation"Biochem.Biophys.Res.Commun. 309. 848-856 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Asao H: "Mechanism of Interleukin 2-induced Siganal Transduction"Yamagata Med.J. 21. 141-154 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 浅尾裕信: "Annual Review免疫2004"中外医学社. 9 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Morita E et al.: "Human parvovirus B19 non-structural protein (NS1) induces cell cycle arrest at G1 phase."J.Virol.. 77. 2915-2921 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kikuchi K et al.: "Identification of AMSH-LP containing a Jab1/MPN domain metalloenzyme motif."Biochem.Biophys.Res.Commun.. 306. 637-643 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kanazawa C et al.: "Effects of deficiencies of STAMs and Hrs, mammalian class E Vps proteins, on receptor downregulation"Biochem.Biophys.Res.Commun.. 309. 848-856 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Asao H.: "Mechanism of Interleukin 2-induced Siganal Transduction."Yamagata Med.J.. 21. 141-154 (2003)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2005-04-19  

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