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Gut, Immune organ-mucosal immunity of gastro-intestinal tract-

Research Project

Project/Area Number 07670867
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・University Hospotal, Assistant Professor, 医学部・附属病院, 講師 (50160875)

Co-Investigator(Kenkyū-buntansha) YAMADA Masao  Okayama University・Medical School, Professor, 医学部, 教授 (40166731)
TANAKA Hiroyuki  Okayama University・Medical School, Assistant Professor, 医学部, 講師 (80231413)
赤在 あゆみ  岡山大学, 医学部・附属病院, 助手 (10231804)
Project Period (FY) 1995 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1997: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1996: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1995: ¥1,400,000 (Direct Cost: ¥1,400,000)
KeywordsImmune organ / Guit epithelial cell / chemokine / IL8 / Ussing chamber / Mast cell / Ussing chamber / IL-8 / MIP-1α / MCP-1 / MCAF / RANTES
Research Abstract

Background and Objective : To clarify a role of the gastrointestinal tract in mediating immunity, we examined following three points between 1995 and 1996, 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-selection 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 1997, 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 lone. Less

Report

(4 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • 1995 Annual Research Report
  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] Megumi ODA: "Modulation of Epithelial Ion Secrotion By Neutrophils and Fibroblasts" Clinical Immunology and Immunopathology. 76・1. S41-S41 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Megumi ODA: "Comparison of Viral vergus Bacteria(-Induced Production of chemokines In Gut Epithelial Cells." Clinical Immunology and Immunopathology. 76・1. S41-S41 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Megumi Oda et al: "Modulation of Epitheloal Ion Secretion By Neutrophils and Fibroblasts" Clinical Immunology and Immunopathology. 76・1. S41-41 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Megumi Oda et al: "Comparison of Viral versus Bacterial-Induced Productin of Chemokines In Gut Epithelial Cells" Clinical Immunology and Immunopathology. 76・1. S42-42 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Megumi ODA: "Modnlation of Epithelial Ion Secretion By Nentrophils and Fibroblasts" Clinical Immunology and Immunopathology. 76・1. S41-S41 (1995)

    • Related Report
      1997 Annual Research Report
  • [Publications] Megumi ODA: "Comparison oof Viral verpus Bacterial-Induced Production of Chemokines In Gut Epithelial Cells" Clinical Immunology and Immunopathology. 76・1. S42-S42 (1995)

    • Related Report
      1997 Annual Research Report
  • [Publications] Megumi ODA: "Modulation of Epithelial Ion Secretion By Nentrophils and Fibroblasts" Clinical Immunology and Immunopathology. 76・1. S41-S41 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] Megumi Oda: "Comparison of Viral vetsus Bacterial - Inducecl Production of Chemokines In Gut Epithelial Cells" Clinical Immunology and Immunopathology. 76・1. S42-S42 (1995)

    • Related Report
      1996 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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