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The roll of mast cell and T lymphocyte in dual asthmatic response using mouse

Research Project

Project/Area Number 08670654
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Respiratory organ internal medicine
Research InstitutionTokyo University

Principal Investigator

ISHII Akira  Faculty of Medicine Tokyo University Assistant Professor, 医学部・附属病院, 助手 (30272553)

Co-Investigator(Kenkyū-buntansha) HIRAI Kohichi  Faculty of Medicine Tokyo University Assistant Professor, 医学部・附属病院, 助手 (10156630)
TAKAISHI Toshiaki  Faculty of Medicine Tokyo University Assistant Professor, 医学部・附属病院, 助手 (40154736)
Project Period (FY) 1996 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1997: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1996: ¥1,000,000 (Direct Cost: ¥1,000,000)
KeywordsAsthma / late asthmatic response / immediate asthmatic response / mast cell / T lymphocyte / mass cell deficient mouse / mouse / マスト細胞欠損マウス / T細胞欠損マウス / 遅発型反応 / I型アレルギー / W / W^V
Research Abstract

After ovalbumin inhalation in sensitized +/+ mice, immediate asthmatic response and late asthmatic response was observed. In sensitized w/wィイD1vィエD1 mice bronchoconstrictive response was not observed in IAR and weak in LAR. This result shows that mast cell might not play an important roll in late asthmatic response, but have some influence on late asthmatic response. Then, what cell does play an important roll in late asthmatic response? To resolve this question I examined the roll of T lymphocyte.
In sensitized mice lacking of T cell late asthmatic response was very weak. In mice which sensitized T cell were imported into, late asthmatic response was observed after ovalbumin inhalation. This result shows that T cell plays an important roll in late asthmatic response. Although the mechanism of airway hyperactivity is unknown, CD4+/T helper (TH2) cell is shown to be very important in many reports. But, in this experiment, between TH1 dominant C57BL6 and TH2 dominant BALB/c mouse there was no difference in late asthmatic response. About this point I will investigate further.
I think this experiment made clear the roll of mast cell and T cell.

Report

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

    (6 results)

All Other

All Publications (6 results)

  • [Publications] 石井 彰: "マウスの気道過敏性亢進に対するマスト細胞の役割" 日本呼吸器学会雑誌. 36. 146 (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] 石井彰、河崎伸: "好中球の気道上皮細胞への接着調節と治療薬物の影響" 日本呼吸器学会雑誌. 36. 323 (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] 石井 彰: "遅発型反応時の気道過敏性亢進に対するI型アレルギー反応の関与" アレルギー. 46(8,9). 888 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 石井彰、中嶋康之: "抗原感作による気道過敏性の亢進に対するGM-CSFの関与" アレルギー. 46(8,9). 888 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 石井彰、幸山正: "好酸球,気道上皮の産生するIL-8に対するホスミシンの効果検討" アレルギー. 46(8,9). 938 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 石井 彰: "マスト細胞欠損マウスにおける遅発型喘息反応の検討" アレルギー. 45巻・8・9号. 893- (1996)

    • Related Report
      1996 Annual Research Report

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Published: 1996-04-01   Modified: 2016-04-21  

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