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Molecular mechanisms that function in oligodendrocyte myelination

Research Project

Project/Area Number 24890291
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field General physiology
Research InstitutionNational Institute for Physiological Sciences

Principal Investigator

SHIMIZU Takeshi  生理学研究所, 分子生理研究系, 助教 (60398237)

Project Period (FY) 2012-08-31 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsオリゴデンドロサイト / ミエリン / グリア細胞
Research Abstract

Oligodendrocytes are glial cells that myelinate neuronal axons in the central nervous system. Myelin insulates axons to increase conduction velocity of neuronal action potentials. Recent studies have shown that mechanical factors influence various cell properties. Mechanical stimulation can be transduced to intracellular biochemical signals through conformational changes in focal adhesion-related mechanosensors. We analyzed oligodendrocyte morphology and myelination in relation with the mechanosensors. In addition, we found that non-canonical Wnt signaling was up-regulated in a demyelinating mouse model. We examined whether non-canonical Wnt signaling pathway had a role in the Experimental Autoimmune Encephalomyelitis-induced neural pathology.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Annual Research Report

URL: 

Published: 2012-11-27   Modified: 2019-07-29  

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