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Mucosal Immunity of gaitro-intestinal tract-making in vitro modol of GI tract

Research Project

Project/Area Number 10670732
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionOKAYAMA UNIVERSITY

Principal Investigator

ODA Megumi  Okayama University, Medical School, Professor, 医学部, 教授 (50160875)

Co-Investigator(Kenkyū-buntansha) YAMADA Masas  Okayama University, Medical School, Professor, 医学部, 教授 (40166731)
NISHIOCHI Ritsus  Okayama University, Medical School Hospital, Assistant, 医学部・附属病院, 助手 (20284119)
TANAKA Hiroyuki  Okayama University, Medical School, Assoc.Professor, 医学部, 助教授 (80231413)
Project Period (FY) 1998 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2000: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1999: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1998: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsImmune organ / gastro intestinal tract / muccsal immunity / chemokine / mast cell / in vitro model
Research Abstract

Background and objective : To clarify a role of the gastrointestinal tract in mediating immunity, we examined following three points between 1998 and 1999, using experiments where gastrointestinal epithelial cells are infected by bacteria and viruses.(1) Whether mRNA of the chemokine family is expressed in epithelial cells, (2) whether the chemokine mRNAs are translated into proteins and (3) whether the chemokine proteins have any functions. As a result, the patterns of chemokines produced by gastrointestinal epithelial cells due to bacterial or viral infections differed from each other, which was thought to be the main cause of the diversity in local mobilization of inflammatory cells and inflammatory responses against various infections. Furthermore, IL-8 obtained from supernatant of cell culture was concentrated, then added to neutrophils and briefly cultured. Subsequently, expression levels of CD11b/18 and Leu8 (L-selectin) on the surface of neutrophils were measured by FACS, resul … More ting in an increase in CD11b/18 and a decrease in L-selectin expression. And anti-IL-8 antibody partially inhibited these increases and decreases, suggesting that IL-8 in supernatant of cell culture plays a role in activating neutrophils. However, other cytokines are also involved.
Then in 2000, we used an Ussing chamber to electrophysiologically analyze the influence of various chemokines and supernatant of cell culture on T84 and/or 18CO (human gastrointestinal fibroblasts) and/or neutrophils coculture systems. In addition, establishment of a mast cell line was attempted, to examine the effects of mast cells instead of neutrophils.
Methods and Results : Coculture of gastrointestinal epithelial cells with fibroblasts facilitated membrane depolarization, and coculture with neutrophils further facilitated depolarization. A mast cell line was established using a culture system where IL-6, stem cell factor and prostaglandin E_2 were added to mononuclear cells from cord blood. We intend to further investigate the coculture system with this cell line.
The pathogenesis and the treatment strategy of 0-157 infection were also investigated. Less

Report

(4 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • 1998 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] 小田慈,萬木章,清野佳紀: "O157による溶血性尿毒症症候群の治療"Annual Review血液1998,医学書院. 50-63 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 小田慈: "病原性大腸菌O157患者の臨床医学的解析"病原性大腸菌O157による疾患の重症化の予防及び治療を目的とした医薬品の開発研究 研究報告書(研究代表者 雨官浩. 113-114 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 小田慈: "病原性大腸菌O157患者の臨床医学的解析"病原性大腸菌O157による疾患の重症化及び治療を目的とした医薬品の開発研究 研究報告書(研究代表者 竹田多恵). 128-129 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 井上拓也,小田慈 他: "腸管出血性大腸菌O-157感染による溶血性尿毒症症候群に胆汁鬱滞反復性尿道感染を合併し、重篤な肝障害をきたした一例"小児感染免疫. (in press). (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] N.Yamashita,M.Oda et al: "Molecular Detection of Metastatic Retinoblastoma Cells by Transcription Polymerase Reaction for Interphotoreceptor Retinoid-binding protein mRNA"Cancer. (in press). (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Megumi Oda: "Clinical analysis of the patients infected by E Coli 0157"Research Report 42282 (Head Investigator H.Amamiya). 113-114 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Megumi Oda: "Clinical evaruation of the patients infected by E.Coli 0157"Research Report 42282 (Head Investigator T.Tae). 128-129 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] T.Inove, M.Oda et al: "Hemolytic Uremic Syndrome caused by E.Celi 0157 Infection -a case repod with severe repatic failure"Infeation and Immunity in childhood. (in press). (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] N Yamashita, M.Oda et al.: "Molecular Detection of Metatatic Retinoblantoma cases by Transcription polymerase Reaction for Interphotoreceptor Retinoid-binding protein mRNA"Cancer. (in press). (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Megumi Oda et al.: "Treatment and pathogenesis of Nemclytic Unmic syndrme caused by E.cili c-157 Annual Review, Blood 1998"Igukushoin, Tokyo. 56-63 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 小田慈: "病原性大腸菌O157患者の臨床医学的解析"病原性大腸菌O157による疾患の重症化及び治療を目的とした医薬品の開発研究 研究報告書(研究代表者 竹田多惠). 128-129 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 小田 慈: "病原性大腸菌O157患者の臨床的解析"病原性大腸菌O157による疾患の重症化の予防及び治療を目的とした医薬品の開発研究 第4分野課題番号42282研究報告書1999. 113-114 (1999)

    • Related Report
      1999 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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