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2013 Fiscal Year Final Research Report

Mechanisms of morphological changes of mitochondria during neural differentiation and under disease condition by using cell-resealing technique

Research Project

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Project/Area Number 23657124
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Cell biology
Research InstitutionThe University of Tokyo

Principal Investigator

MURATA Masayuki  東京大学, 総合文化研究科, 教授 (50212254)

Project Period (FY) 2011 – 2012
Keywordsシグナル伝達 / 神経科学 / 細胞・組織 / セミインタクト細胞
Research Abstract

We established a neural cell line N14.5-Tom5 cells, in which mitochondrial protein GFP-Tom5 is stably expressed. By using N14.5-Tom5, we found that activation of GSK3beta or Akt was involved in mitochondrial fission during neural differentiation, and identified the phosphorylation of Drp1, dynamin-related GTPase, by GSK3beta regulated the fission. Interestingly, the phosphorylation of Drp1 is reported be required for the mitochondrial fission at the onset of mitosis in mammalian cells. Next, we constructed model cells that replicated the conditions in neurons of Alzheimer's disease by using the resealing-cell technique and cytosol prepared from ApoE(-/-) mouse. As a result, we found that inactivity of Akt in the model cells caused the elongation of mitochondria and resulted in depressed mitochondrial function. Collectively, the persistent phosphorylation of both GSK3beta and Akt plays a crucial role for the maintaining normal mitochondrial morphology and function.

  • Research Products

    (13 results)

All 2013 2012

All Journal Article (8 results) (of which Peer Reviewed: 4 results) Presentation (5 results)

  • [Journal Article] PPARγ-induced PARylation promotes local DNA demethylation by production of 5-hydroxymethylcytosine2013

    • Author(s)
      Fujiki, K., Shinoda, A., Kano, F., Sato, R., Shirahige, K., Murata, M
    • Journal Title

      Nature Communications

      Volume: 4 Pages: 2262

    • DOI

      10.1038/ncomms3262

    • Peer Reviewed
  • [Journal Article] The Semi-Intact Cell System and Methods for Cell Resealing : a Novel Systems Biology Tool to Elucidate Protein Networks with Spatio-Templioral Information2013

    • Author(s)
      Kano, F., Murata, M
    • Journal Title

      Advances in Systems Biology

      Volume: 2(1) Pages: 6-14

    • Peer Reviewed
  • [Journal Article] A Resealed-Cell System for Analyzing Pathogenic Intracellular Events : Perturbation of Endocytic Pathways under Diabetic Conditions2012

    • Author(s)
      Kano, F., Nakatsu, D., Noguchi, Y., Yamamoto, A., Murata, M
    • Journal Title

      PLoS ONE

      Volume: 7(8) Pages: e44127

    • DOI

      10.1371/journal.pone.0044127

    • Peer Reviewed
  • [Journal Article] 哺乳動物細胞ゴルジ体の細胞周期依存的ディスアッセンブリー2012

    • Author(s)
      加納ふみ, 村田昌之
    • Journal Title

      生体の科学

      Volume: 63巻5号 Pages: 404-407

  • [Journal Article] 新しい機能を問われ出した小胞体-ゴルジ体中間区画 (ER-Golgi intermediate compartment : ERGIC)2012

    • Author(s)
      菅原太一, 加納ふみ, 村田昌之
    • Journal Title

      生体の科学

      Volume: 63巻5号 Pages: 424-425

  • [Journal Article] セミインタクト細胞リシール法を用いた「病態モデル細胞」作製とその疾患研究への応用2012

    • Author(s)
      村田昌之, 加納ふみ
    • Journal Title

      化学と生物

      Volume: Vol.50(No.7) Pages: 510-517

  • [Journal Article] PKCd and e regulate the morphological integrity of the ER-Golgi intermediate compartment (ERGIC) but not the anterograde and retrograde transports via the Golgi apparatus2012

    • Author(s)
      Sugawara, T., Nakatsu, D., Kii, H., Maiya, N., Adachi, A., Yamamoto, A., Kano, F., Murata, M
    • Journal Title

      Biochem. Biophys. Acta (Molecular Cell Research)

      Volume: 1823(4) Pages: 861-875

    • Peer Reviewed
  • [Journal Article] Semi-intact cell system : Application to the nalysis of membrane trafficking beween the endoplasmic reticulum and the Golgi apparatus and of cell cycle-dependent changes in the morphology of these organelles2012

    • Author(s)
      Murata, M., Kano, F
    • Journal Title

      in Crosstalk and Integration of Membrane Trafficking Pathways

  • [Presentation] セミインタクト細胞リシール技術を用いた糖尿病モデル細胞の構築2013

    • Author(s)
      野口 誉之, 堀内 雄太, 中津 大貴, 加納 ふみ, 村田 昌之
    • Organizer
      第51回日本生物物理学会年会
    • Place of Presentation
      京都国際会議場
    • Year and Date
      2013-10-29
  • [Presentation] Disease model cell system : a novel proteomics tool to elucidate protein networks with spatio-temporal information2013

    • Author(s)
      Fumi Kano, Daiki Nakatsu, Yoshiyuki Noguchi, Yuta Horiuchi, Masayuki Murata
    • Organizer
      The 12th Human Proteome Organization Congress
    • Place of Presentation
      Yokohama, Japan
    • Year and Date
      2013-09-16
  • [Presentation] セミインタクト細胞リシール法を用いた病態モデル細胞の創成2013

    • Author(s)
      加納ふみ, 村田昌之
    • Organizer
      第65回日本細胞生物学会大会.シンポジウム「細胞への蛋白質導入技術と蛋白質イメージング技術」
    • Place of Presentation
      ウインクあいち
    • Year and Date
      2013-06-19
  • [Presentation] セミインタクト細胞リシール技術を用いた糖尿病モデル細胞の構築 : 病態依存的なエンドサイトーシス攪乱2013

    • Author(s)
      堀内雄太, 加納ふみ, 野口誉之, 村田昌之
    • Organizer
      第65回日本細胞生物学会大会(名古屋)
    • Year and Date
      2013-06-19
  • [Presentation] A Resealed-Cell System for Analyzing Pathogenic Intracellular Events : Insight into Signal Transduction Cascade in Hyperlipidemic or Diabetic Cells2012

    • Author(s)
      Masayuki Murata, Fumi Kano
    • Organizer
      The 25th Annual and International Meeting of the Japanese Association for Animal Cell Technology (JAACT2012)
    • Place of Presentation
      Nagoya Congress Center, Nagoya, Japan
    • Year and Date
      2012-11-27

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Published: 2015-06-25   Modified: 2023-03-16  

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