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The study for cerebellar cortical information processing using functional imaging and three-dimensional reconstruction

Research Project

Project/Area Number 24500476
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Fusional basic brain science
Research InstitutionThe Institute of Physical and Chemical Research (2013-2014)
Saitama University (2012)

Principal Investigator

MICHIKAWA TAKAYUKI  独立行政法人理化学研究所, 光量子工学研究領域, 研究員 (90282516)

Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Keywordsカルシウムイメージング / 国際情報交換
Outline of Final Research Achievements

Adenovirus can be used to express genetically encoded calcium indicators into specific types of neurons, such as cerebellar Purkinje cells. In vivo two-photon imaging of a large population of Purkinje cells will be useful to identify functional circuits that participate in information processing in cerebellar cortex. In this study, I have established experimental procedures and deconvolution-based data analysis methods suitable for inferring single complex spike firings of Purkinje cells from two-photon calcium imaging data acquired from living mice expressing a genetically encoded ratiometric calcium indicator, yellow cameleon 2.60.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report

Research Products

(8 results)

All 2014 2013 2012

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 1 results) Presentation (5 results)

  • [Journal Article] Phospholipase C-β1 and β4 contribute to non-genetic cell-to-cell variability in histamine-induced calcium signals in HeLa cells2014

    • Author(s)
      Ishida S, Matsu-Ura T, Fukami K, Michikawa T, Mikoshiba K.
    • Journal Title

      PloS One

      Volume: 9

    • DOI

      10.1371/journal.pone.0086410

    • Related Report
      2013 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Optimal microscopic systems for long-term imaging of intracellular calcium using a ratiometric genetically-encoded calcium indicator.2014

    • Author(s)
      Miyamoto A, Bannai H, Michikawa T, Mikoshiba K.
    • Journal Title

      Biochem Biophys Res Commun.

      Volume: 434 Pages: 252-257

    • DOI

      10.1016/j.bbrc.2013.02.112

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Cooperative and stochastic calcium releases from multiple calcium puffsites generate calcium microdomains in intact HeLa cells.2012

    • Author(s)
      Nakamura H, Bannai H, Inoue T, Michikawa T, Sano M, Mikoshiba K.
    • Journal Title

      Journal of Biological Chemistry

      Volume: 287 Pages: 24563-24572

    • DOI

      10.1074/jbc.m111.311399

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] Optical recording of neural activity using yellow cameleon 2.60-expressing mice2014

    • Author(s)
      Michikawa, T, Itohara, S., and Miyawaki, A,
    • Organizer
      理研シンポジウム:第2回「光量子工学研究」
    • Place of Presentation
      仙台市情報・産業プラザ 5階多目的ホール
    • Year and Date
      2014-11-25 – 2014-11-26
    • Related Report
      2014 Annual Research Report
  • [Presentation] Cell-type selective wide-field calcium imaging, combined Yellow Cameleon 2.60 Tg mice and macromicroscopy2013

    • Author(s)
      Kuroki, S., Tsutsui H., Michikawa T., Iwama M., Miyawaki A. and Itohara S.
    • Organizer
      日本神経科学会大会
    • Place of Presentation
      国立京都国際会館
    • Related Report
      2013 Research-status Report
  • [Presentation] In vivo calcium dynamics in cerebellar Purkinje cell dendrites2012

    • Author(s)
      Michikawa, T., Miyawaki, A., Kakei, S., Hausser, M., Itohara, S. and Nakai, J.
    • Organizer
      Society for Neuroscience
    • Place of Presentation
      New Orleans, USA
    • Related Report
      2012 Research-status Report
  • [Presentation] Cell-type selective wide-field calcium imaging, combined Yellow Cameleon 2.60 Tg mice and macromicroscopy2012

    • Author(s)
      Kuroki, S., Michikawa, T., Tsutsui, H., Manita, S., Shimozono, S., Murayama, M., Miyawaki, A. and Itohara, S
    • Organizer
      Molecular and Cellular Cognition Society
    • Place of Presentation
      New Orleans, USA
    • Related Report
      2012 Research-status Report
  • [Presentation] Establishment of transgenic mice expressing calcium sensor Yellow Cameleon 2.60 and applications to analysis of the thalamocortical pathway2012

    • Author(s)
      Kuroki, S., Michikawa, T., Manita, S., Tsutsui, H., Shimozono, S., Murayama, M., Miyawaki, A. and Itohara, S
    • Organizer
      日本神経科学会
    • Place of Presentation
      名古屋
    • Related Report
      2012 Research-status Report

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Published: 2013-05-31   Modified: 2019-07-29  

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