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Identification and elucidation of functional relationship between neuronal exosomal ncRNA and Lewy body dementia

Research Project

Project/Area Number 25890012
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Neurophysiology / General neuroscience
Research InstitutionOsaka University

Principal Investigator

KAWAHARA Hironori  大阪大学, 免疫学フロンティア研究センター, 特任研究員 (00424177)

Project Period (FY) 2013-08-30 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywordsexosome / α-synuclein / IP3 / ncRNA / 脳神経疾患
Outline of Final Research Achievements

Exosome is not only signal small vesicle which is utilized as cell-cell communication in various cells but also in neuronal cells. However, it remains unclear that the mechanisms by which neuronal exosomes are propagated within neuronal cells, particularly under IP3-stimulation. Novel lncRNAs (long non-coding RNAs) and proteins which were incorporated into IP3-stimulated exosomes were identified in mouse primary neurons. α-synuclein was efficiently incorporated into exosomes by Rpn1, and then efficiently transferred to glia cells via exosomes.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Annual Research Report
  • Research Products

    (1 results)

All 2014

All Presentation (1 results)

  • [Presentation] 神経系エキソソームを介した新規グリア細胞応答因子の探索2014

    • Author(s)
      河原裕憲 奥野龍禎 望月秀樹 華山力成
    • Organizer
      第37回 神経科学学会
    • Place of Presentation
      横浜市
    • Year and Date
      2014-09-11 – 2014-09-13
    • Related Report
      2014 Annual Research Report

URL: 

Published: 2013-09-12   Modified: 2019-07-29  

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