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Identification of therapeutic targets and drug discovery research for Dravet syndrome using iPSCs model

Research Project

Project/Area Number 26860833
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pediatrics
Research InstitutionFukuoka University

Principal Investigator

Tanaka Yasuyoshi  福岡大学, てんかん分子病態研究所, ポスト・ドクター (50714466)

Research Collaborator SASAGURI Yukari  
Project Period (FY) 2014-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
KeywordsDravet症候群 / SCN1A / iPS細胞 / TALEN / ゲノム編集 / 興奮性神経 / 抑制性神経 / Dravte症候群 / てんかん / 疾患iPS細胞モデル / ドラベ症候群 / 遺伝子編集 / 疾患モデル / 神経分化 / genome editing / GABA作動性神経 / 遺伝子修復
Outline of Final Research Achievements

In order to contribute to deciphering the pathogenic mechanisms and facilitating drug discovery for Darvet syndrome (DS), we established 1) patient-derived iPSCs, 2) generated an isogenic control cell line derived from DS patient iPSCs by genome editing using TALEN method, and 3) investigated the functional differences in neuronal cells between control and DS cells via functional analysis of action potential measurement.
In this study, we generated iPSC lines derived from three DS patients. To establish isogenic control cells, we generated a genome-edited control cell line from one of the DS iPSC lines by substituting the point mutation with the wild-type residue using TALEN. This artificial control iPSC line will be a powerful tool for research into the pathology of DS. We measured action potential in iPSC-derived excitatory neurons by use of a microelectrode array system. The results of this study can be applied to research for drug discovery and development against DS.

Report

(5 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (7 results)

All 2018 2016 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (6 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene2018

    • Author(s)
      Tanaka Yasuyoshi、Sone Takefumi、Higurashi Norimichi、Sakuma Tetsushi、Suzuki Sadafumi、Ishikawa Mitsuru、Yamamoto Takashi、Mitsui Jun、Tsuji Hitomi、Okano Hideyuki、Hirose Shinichi
    • Journal Title

      Stem Cell Research

      Volume: 28 Pages: 100-104

    • DOI

      10.1016/j.scr.2018.01.036

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] Generation of isogenic iPS cell line model for Dravet syndrome using TALEN-mediated genome editing of SCN1A gene2016

    • Author(s)
      Y. Tanaka, T. Sone, N. Higurashi, T. Uchida, M. Ishikawa, H. Okano, S. Hirose
    • Organizer
      the 21st Korean Epilepsy Congress (KEC 2016)
    • Place of Presentation
      Seoul (Korea)
    • Year and Date
      2016-06-17
    • Related Report
      2016 Research-status Report
    • Int'l Joint Research
  • [Presentation] What was revealed by whole genome sequence analysis of genome edited patient-derived disease iPSCs.2015

    • Author(s)
      Takefumi Sone, Sung-Joon Park, Yasuyoshi Tanaka, Etsuro Ohta, Norimichi Higurashi, Kenta Nakai, Shinichi Hirose, Hideyuki Okano.
    • Organizer
      BMB2015
    • Place of Presentation
      横浜(日本)
    • Year and Date
      2015-12-01
    • Related Report
      2015 Research-status Report
  • [Presentation] TALEN-mediated genome editing of patient-derived iPSCs for disease model studies.2015

    • Author(s)
      Takefumi Sone, Yasuyoshi Tanaka, Etsuro Ohta, Makoto Hosoya、Naoki Ichiyanagi, Tetsuya Akiyama, Norimichi Higurashi、Shinichi Hirose, Hideyuki Okano.
    • Organizer
      Conference on Transposition and Genome Engineering 2015
    • Place of Presentation
      奈良(日本)
    • Year and Date
      2015-11-17
    • Related Report
      2015 Research-status Report
  • [Presentation] Genome editing of SCN1A in induced pluripotent stem cells to study the pathomechanisms of Dravet syndrome.2015

    • Author(s)
      Yasuyoshi Tanaka, Takehumi Sone, Norimichi Higurashi, Taku Uchida, Mitsuru Ishikawa, Hideyuki Okano, Shinichi Hirose.
    • Organizer
      13th AOCCN
    • Place of Presentation
      台北 (台湾)
    • Year and Date
      2015-05-14
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] TALEN-mediated genome editing of patient-derived iPSCs for disease model studies2015

    • Author(s)
      Takefumi sone, Yasuyoshi Tanaka, Etsuro Ohta, Naoki Ichiyanagi, Norimichi Higurashi, Shinichi Hirose, Hideyuki Okano
    • Organizer
      第14回日本再生医療学会総会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2015-03-18 – 2015-03-22
    • Related Report
      2014 Research-status Report
  • [Presentation] TALEN-mediated genome editing of patient-derived iPSCs for disease model studies2014

    • Author(s)
      Takefumi sone, Yasuyoshi Tanaka, Etsuro Ohta, Naoki Ichiyanagi, Norimichi Higurashi, Shinichi Hirose, Hideyuki Okano
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-11-24 – 2014-11-29
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2019-03-29  

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