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Necessary environment for amelioration after ischemic reperfusion injury in brain: the role of L-serine

Research Project

Project/Area Number 15K19497
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Neurology
Research InstitutionKeio University

Principal Investigator

Suzuki Masataka  慶應義塾大学, 医学部(信濃町), 特任助教 (90595000)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Keywords虚血再灌流障害 / L-セリン / PHGDH / 脳虚血再灌流障害 / D-セリン / 脳虚血再韓流障害 / アストロサイト
Outline of Final Research Achievements

In this study, I aimed to clarify how L-serine , which is suplied by astroglia, affects on neurogenesis after ischemic reperfusion injury in brain of MCAO mouse model. The size of infarct region after MCAO in Astroglia specific knock out of phosphoglycerate dehydrogenase (PHGDH) was not significantly different from that in flox/flox mice. L-serine activated phosphorylation of p70S6K in primary cortical neurons in vitro. Because p70S6K is the protein that facilitates protein synthesis and cell proliferation, L-serine possibly stimulates neurogenesis.

Report

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

    (1 results)

All 2016

All Presentation (1 results)

  • [Presentation] Excessive D-serine mediates cell death in developing neuron2016

    • Author(s)
      鈴木将貴、笹部潤平、相磯貞和
    • Organizer
      Society for Neuroscience 2016
    • Place of Presentation
      サンディエゴ(アメリカ)
    • Year and Date
      2016-11-12
    • Related Report
      2016 Annual Research Report

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

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