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Optical cleaning method of living animal skull for 2photon imaging

Research Project

Project/Area Number 15K13376
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Optical engineering, Photon science
Research InstitutionThe University of Tokyo

Principal Investigator

Onodera Hiroshi  東京大学, 大学院工学系研究科(工学部), 特任教授 (20214207)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords臓器透明化 / 神経科学 / 情報伝達機構 / 透明化技術 / 脳活動リアルタイム観察 / GCAMP / 臓器透明化技術 / 神経生理学 / レーザー顕微鏡
Outline of Final Research Achievements

The aim of this study is to clarify skull bone of mice in order to analyze neuronal network in the cerebral cortex of living animal. First, we successfully optically cleaned mouse skull bone in vitro by using cleaning agent LUCID-vivo. Then we applied the LUCID-vivo solution on living mouse skull bone for 24 hours. We could observe cerebral cortex and blood vessels on the cortex through transparent skull bones. Neuronal networks of the cerebral cortex were visualized by using transgenic mice (GCAMP). This method can be applicable for many research fields, such as memory, motor function, sensory function, and emotion.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • Research Products

    (5 results)

All 2016

All Journal Article (4 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 3 results,  Open Access: 3 results) Presentation (1 results)

  • [Journal Article] Ultraflexible organic amplifier with biocompatible gel electrodes2016

    • Author(s)
      Tsuyoshi Sekitani, Tomoyuki Yokota, Kazunori Kuribara, Martin Kaltenbrunner, Takanori Fukushima, Yusuke Inoue, Masaki Sekino, Takashi Isoyama, Yusuke Abe Hiroshi, Onodera and Takao Someya
    • Journal Title

      Nature Communications

      Volume: 7 Issue: 1 Pages: 11425-11425

    • DOI

      10.1038/ncomms11425

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Dendrigraft polylysine coated-poly(glycolic acid) fibrous scaffolds for hippocampal neurons2016

    • Author(s)
      Kojima C, Nishioka E, Imai T, Nakahira A, Onodera H
    • Journal Title

      J Biomedical Materials Research

      Volume: 119 Issue: 33 Pages: 2744-2750

    • DOI

      10.1021/acs.jpcb.5b01553

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Optogenetic activation of leptin- and glucoseregulated GABAergic neurons in dorsomedial hypothalamus promotes food intake via inhibitory synaptic transmission to paraventricular nucleus of hypothalamus.2016

    • Author(s)
      Zesemdorj Otgon-Uul , Shigetomo Suyama, Hiroshi Onodera, Toshihiko Yada.
    • Journal Title

      Molecular Metabolism

      Volume: 5 Issue: 8 Pages: 709-715

    • DOI

      10.1016/j.molmet.2016.06.010

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Ultraflexible organic amplifier with biocompatible gel electrodes2016

    • Author(s)
      Tsuyoshi Sekitani, Tomoyuki Yokota, Kazunori Kuribara,w, Martin Kaltenbrunner, Takanori Fukushima,Yusuke Inoue, Masaki Sekino, Takashi Isoyama, Yusuke Abe, Hiroshi Onodera, Takao Someya
    • Journal Title

      Nature Communications

      Volume: in press

    • Related Report
      2015 Research-status Report
  • [Presentation] In vivoでのマウス 頭蓋骨 透明化 に向けた骨片透明化2016

    • Author(s)
      鳴海紘也,小野寺宏
    • Organizer
      応用物理学会秋季学術講演会
    • Place of Presentation
      新潟市
    • Year and Date
      2016-09-13
    • Related Report
      2016 Annual Research Report

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Published: 2015-04-16   Modified: 2018-03-22  

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