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Functional analysis of the intrinsic factors regulating diversity of neural crest cells and disease.

Research Project

Project/Area Number 18590387
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionAichi Medical University

Principal Investigator

IWASHITA Toshihide  Aichi Medical University, Medicine, Associate professor (00283432)

Co-Investigator(Kenkyū-buntansha) KUROKAWA Kei  Aichi medical University, Medicine, Research Associate (90399030)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥300,000)
Fiscal Year 2007: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2006: ¥2,600,000 (Direct Cost: ¥2,600,000)
KeywordsNeural crest / Stem cells / ヒルシュスプルング病
Research Abstract

We have postulated that Hox proteins were candidate for the intrinsic factors that make difference between vagal neural crest and trunk neural crest. To understand the molecular mechanism of the neural crest differentiation by Hox protein, Hox genes were over-expressed in the migrating neural crest. Especially, we focused on the function of HoxB8 that was predominantly expressed by vagal neural crest. HoxB8 and GFP were over-expressed in the migrating chicken vagal neural crest derived from posterior hindbrain using ovo-electroporation technique. The neural crest expressing HoxB8 and GFP protein was also stained by anti-HNK1 antibody that specifically recognized neural crest. Interestingly, Ret, a receptor of glial cell-line derived neurotrophic factor and played an important role on migration of vagal neural crest to gut, was much suppressed in the neural crest expressing HoxB8.

Report

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

    (5 results)

All 2009 2007

All Journal Article (4 results) (of which Peer Reviewed: 3 results) Presentation (1 results)

  • [Journal Article] Galanin receptor subtype 2 suppresses cell proliferation and induces apoptosis in p53 mutant head and neck cancer cells.2009

    • Author(s)
      Kanazawa T
    • Journal Title

      Clinical Cancer Research 15

      Pages: 2222-2230

    • 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] Galanin and galanin receptor type 1 suppress proliferation in squamous carcinoma cells : activation of the extracellular signal regulated kinase pathway and induction of cyclin-dependent kinase inhibitors.2007

    • Author(s)
      Kanazawa T
    • Journal Title

      Oncogene 26

      Pages: 5762-5771

    • 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] Galanin and galanin receptor type 1 suppress proliferation in squamous carcinoma cells: activation of the extracellular signal regulated kinase pathway and induction of cyclin-dependent kinase inhibitors.2007

    • Author(s)
      Kanazawa T
    • Journal Title

      Oncogene 26

      Pages: 5762-5771

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Galanin and galanin receptor type 1 suppress proliferation insquamous carcinoma cells: activation of the extracellular signal regulated kinase pathway and induction of cyclin-dependent kinase inhibitors.2007

    • Author(s)
      Kanazawa T, Iwashita T., et. al.
    • Journal Title

      Oncogene 26

      Pages: 5762-5771

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Presentation] SLAM family receptorによるHematopoietic stem cellsとprogenitor cellsの同定2007

    • Author(s)
      岩下寿秀、黒川景、吉川和宏、佐賀信介
    • Organizer
      第96回日本病理学会総会
    • Place of Presentation
      大阪国際会議場
    • Year and Date
      2007-09-14
    • Related Report
      2007 Annual Research Report

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

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