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Analysis of IL-7 receptor and application for biological protection

Research Project

Project/Area Number 18580309
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Applied veterinary science
Research InstitutionKyoto University

Principal Investigator

MAKI Kazushige  Kyoto University, Institute for Virus Research, Lecturer (10311424)

Co-Investigator(Kenkyū-buntansha) IKUTA Koichi  Kyoto University, Institute for Virus Research, Professor (90193177)
UEDA Masamichi  Kyoto University, Institute for Virus Research, Assistant Professor (50115797)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,890,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥390,000)
Fiscal Year 2007: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2006: ¥2,200,000 (Direct Cost: ¥2,200,000)
KeywordsCytokine / Signal transduction / γδ T cell / Glucocorticold / γδ T細胞 / 樹状細胞
Research Abstract

The IL-7R plays an essential role in γδ T cell development by inducing V-I recombination of the TCRγ locus through STAT5. Although the tyrosine residues in the intracellular domain of the mouse IL-7Rα chain (IL-7Rα) have been implicated in STAT5 activation, it is still enigmatic whether the residues are essential for γδ T cell development. In this study, we revealed that the tyrosine residues of IL-7Rα are dispensable for γδ T cell development, because the mutant IL-7Rα with four intracellular tyrosine residues replaced with phenylalanine (IL-7R-FFFF) partially rescued yd T cell development from IL-7Rα^<-/-> progenitors. We found that 4R/7R-FFFF induced TCRγ germline transcription and STAT5 activation. In addition, we found that the treatment with MEK1/2 inhibitor decreased the levels of TCRγ germline transcription and STAT5 tyrosine phosphorylation by 4R/7R-FFFF, suggesting that MEK1/2 plays an alternative role in STAT5 activation by IL-7R.
Expression of the IL-7Rα is strictly regulated during development and maturation of lymphocytes. While T cells express the IL-7Rα in the periphery, B cells do not. Although GCs induce the transcription of IL-7Rα gene in T cells, their effect on B cells is largely unknown. We found that GCs induce the transcription and expression of IL-7Rα in mouse peripheral B cells. This effect does not require de novo protein synthesis, because a protein synthesis inhibitor, cycloheximide, does not block the transcription. IL-7R signal pathway is intact in peripheral B cells because Stat5, one of the signal molecules of the IL-7Rα, is phosphorylated by IL-7 stimulation. Furthermore, GC-induced IL-7Rα can transmit survival signal in B cells. Therefore, this study demonstrates that GCs induce the transcription and expression of functional IL-7Rα in peripheral B cells, and implies a potential role of the IL-7R in survival of B cells.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (15 results)

All 2008 2007 2006 Other

All Journal Article (8 results) (of which Peer Reviewed: 4 results) Presentation (4 results) Book (1 results) Remarks (2 results)

  • [Journal Article] Transcriptional activation of mouse TCR Jγ 4 germline promoter by STAT5.2008

    • Author(s)
      Masui, N., Tani-ichi, Maki, K., and Ikuta, K
    • Journal Title

      Molecular Immunology 45

      Pages: 849-855

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Transcriptional activation of mouse TCR Jγ4 germline promoter by STAT52008

    • Author(s)
      Masui, N., Tani-ichi, Maki, K., Ikuta, K
    • Journal Title

      Molecular Immunology 45(3)

      Pages: 849-855

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Transcriptional activation of mouse TCR Jγ 4 germline promoter by ST AT5.2008

    • Author(s)
      Masui, N., Tani-ichi, Maki, K., and Ikuta, K
    • Journal Title

      Molecular Immunology 45

      Pages: 849-855

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Induction of the IL-7 receptor α chain in mouse peripheral B cells by glucocorticoids2007

    • Author(s)
      Shibata, H., Tani-ichi, S., Lee, H.-C., Maki, K., and Ikuta, K.
    • Journal Title

      Immunology letter 111

      Pages: 45-50

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Induction of the IL-7 receptor a chain in mouse peripheral B cells by glucocorticoids2007

    • Author(s)
      Shibata, H., Tani-ichi, S., Lee, H.C., Maki, K., Ikuta, K
    • Journal Title

      Immunology letter 111(1)

      Pages: 45-50

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Induction of the IL-7 receptor a chain in mouse peripheral B cells by glucocorticoids2007

    • Author(s)
      Shibata, H., Tani-ichi, S., Lee, H. -C., Maki, K., and Ikuta, K.
    • Journal Title

      Immunology letter 111

      Pages: 45-50

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Role of IL-7 in T cell development2006

    • Author(s)
      Maki, K
    • Journal Title

      Clinical Immunology and Allergy 45(6)

      Pages: 446-451

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Induction of the IL-7 receptor α chain in mouse peripheral B cells by glucocorticoids

    • Author(s)
      Shibata, H., Tani-ichi, S., Lee, H.-C., Maki, K., Ikuta, K.
    • Journal Title

      Immunology letter (印刷中)

    • Related Report
      2006 Annual Research Report
  • [Presentation] IL-7RシグナルによるMEKを介したTCRγ遺伝子座のV-J組換え制御機構の解析2006

    • Author(s)
      真木一茂、生田宏一
    • Organizer
      第36回日本免疫学会
    • Place of Presentation
      大阪(大阪国際会議場)
    • Year and Date
      2006-12-13
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] MEK1/2 controls the accessibility of the TCRγ Locus in IL-7R signaling2006

    • Author(s)
      Maki, K., Hayashi, S., Ikuta, K
    • Organizer
      The 36th Annual Meeting of the Japanese Society for Immunology
    • Place of Presentation
      Osaka
    • Year and Date
      2006-12-13
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] The IL-7 Receptor Controls the Accessibility of the TCRγ Locus by MAPK Pathway2006

    • Author(s)
      Maki, K., Hayashi, S and Ikuta, K
    • Organizer
      20th International Congress of Biochemistry and Molecular Biology and 11th FAOBMB Congress
    • Place of Presentation
      京都(京都国際会館)
    • Year and Date
      2006-06-21
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] The IL-7 Receptor Controls the Accessibility of the TCRγ Locus by MAPK Pathway2006

    • Author(s)
      Maki, K., Hayashi, S., Ikuta, K
    • Organizer
      20th International Congress of Biochemistry and Molecular Biology and 11th FAOBMB Congress
    • Place of Presentation
      Kyoto
    • Year and Date
      2006-06-21
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Book] 臨床免疫アレルギー科「T細胞分化とIL-7」2006

    • Author(s)
      真木一茂
    • Total Pages
      114
    • Publisher
      科学評論社
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Remarks]

    • URL

      http://www.virus.kyoto-u.ac.jp/Lab/ikuta.html

    • Related Report
      2007 Final Research Report Summary
  • [Remarks]

    • URL

      http://www.virus.kyoto-u.ac.jp/Lab/ikuta.html

    • Related Report
      2007 Annual Research Report

URL: 

Published: 2006-04-01   Modified: 2016-04-21  

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