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Study for mechanism of neural tube defect with cell culture system

Research Project

Project/Area Number 19K07833
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 51030:Pathophysiologic neuroscience-related
Research InstitutionFujita Health University

Principal Investigator

Omi Minoru  藤田医科大学, 医学部, 助教 (00400416)

Project Period (FY) 2019-04-01 – 2022-03-31
Project Status Completed (Fiscal Year 2021)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2021: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2020: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2019: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords神経発生 / 神経管 / 神経 / ES細胞
Outline of Research at the Start

神経管異常(NTD)は1000人に1から2人の高確率で起こる中枢神経組織の先天異常である。NTDはさまざまな機能障害を引き起こし、重篤な場合では死に至る場合もあるが、その発症機構はいまだ解明されていない。抗てんかん薬として使用されるバルプロ酸(VPA)は胎児に作用するとNTDを引き起こす。本研究ではVPAの作用機構を解析することで、神経管発生機構やNTD発症機構の解明を目指す。

Outline of Final Research Achievements

Neural tube defect is a congenital disease and causes serious problems like movement disorder. As its incidence rate is high, 0.1 - 0.2%, therapies for this disease have to be developed as soon as possible.
Valproic acid is a chemical which induces neural tube defect in embryos of human and mouse. To elucidate the mechanism of the neural tube defect, effects of valproic acid on neural cells were studied. When cultured neural cells derived from es cells were treated with valproic acid, cell death was increased. RNA-seq analysis indicated over one thousand genes that were affected by valproic acid. One of the gene was overexpressed, cell death was increase. On the other hand, downregulation of the gene with shRNA show tendency of cell death suppression. These results suggest that valproic acid may cause neural tube defect by inducing cell death and that the picked-up gene may mediate the effect of valproic acid.

Academic Significance and Societal Importance of the Research Achievements

神経管異常は中枢神経の先天的形成異常であり、脊椎二分症や脳ヘルニアといった中枢神経の奇形を引き起こし、運動機能などに支障を来す。重篤な場合では出生直後に死にいたる。神経管異常の発症率は0.1%から0.2%と極めて高く、生涯にわたって健康面に問題を抱え続けることになるため、その発症機構の解明および予防法や治療法の開発は医学的にも社会的にも重要な課題である。本研究では神経管異常を誘発するバルプロ酸を用い解析を行ったところ、バルプロ酸は神経細胞死を誘発している可能性が示唆された。また、その作用を介在する遺伝子が候補として挙げられた。これらの結果は神経管異常の仕組みの解明や予防に資すると考えられる。

Report

(4 results)
  • 2021 Annual Research Report   Final Research Report ( PDF )
  • 2020 Research-status Report
  • 2019 Research-status Report
  • Research Products

    (2 results)

All 2021

All Journal Article (2 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 2 results,  Open Access: 1 results)

  • [Journal Article] Cross‐talk between EGFR and BMP signals regulates chondrocyte maturation during endochondral ossification2021

    • Author(s)
      Lees‐Shepard John B.、Flint Kaitlyn、Fisher Melanie、Omi Minoru、Richard Kelsey、Antony Michelle、Chen Po Jung、Yadav Sumit、Threadgill David、Maihle Nita J.、Dealy Caroline N.
    • Journal Title

      Developmental Dynamics

      Volume: 251 Issue: 1 Pages: 75-94

    • DOI

      10.1002/dvdy.438

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Mutually repulsive EphA7-EfnA5 organize region-to-region corticopontine projection by inhibiting collateral extension2021

    • Author(s)
      1.Iguchi, T., Oka, Y., Yasumura, M., Omi, M., Kuroda, K.,Yagi, H., Xie, MJ., Taniguchi, M., Bastmeyer, M., Sato, M.
    • Journal Title

      J. Neurosci.

      Volume: Online ahead of print Issue: 22 Pages: 4795-4808

    • DOI

      10.1523/jneurosci.0367-20.2021

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research

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Published: 2019-04-18   Modified: 2023-01-30  

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