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Molecular-biological Research for Neuron-Glial Interaction during retinal regeneration.

Research Project

Project/Area Number 13671854
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Ophthalmology
Research InstitutionTokyo Women's Medical University

Principal Investigator

KITANO Shigehiko  Tokyo Women's Medical University, School of Medicine, Professor, 医学部, 教授 (30161483)

Co-Investigator(Kenkyū-buntansha) SEKIMOTO Kaori  Tokyo Women's Medical University, School of Medicine, Associate, 医学部, 助手 (10307499)
FUNATSU Hideharu  Tokyo Women's Medical University, School of Medicine, Assistant Professor, 医学部, 講師 (50181441)
Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2002: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2001: ¥1,700,000 (Direct Cost: ¥1,700,000)
KeywordsRetinal Ganglion Cells / Glial cells / Retinal regeneration / Neurotrophin / Cytokine / ニューロトロフィン / 虚血 / 興奮性アミノ酸 / 一酸化窒素合成酵素
Research Abstract

The cytotoxic effects of hypoxia and excitatory amino acids on cultured retinal ganglion cells (RGCs) were studied. And the influence of coculture with retinal Muller glia and cortical astrocytes on cell survival was evaluated. The results from our culture model demonstrate the importance of the neuron-glial interaction in determining cellular viability. Glial cells seem to play an important role in the response to hypoxia and excitotoxicity.
Nitric oxide may mediate hypoxic and excitotoxic effects on central neurons. In this culture, the glial cell monolayer is bNOS positive and iNOS negative immunohistochemically. The effect of a nitric oxide synthase (NOS) inhibitor, Nω-nitro-L-arginine (NA), on survival of culture rat retinal ganglion cells subjected to hypoxia and excitotoxicity were investigated. The survival rate of cultured RGCs exposed to hypoxia and excitatory amino acids increased in a dose-dependent fashion with NA. The time course of the survival rate of RGC cultures pretreated with NA showed a better survival rate. A NOS inhibitor provides partial protection of RGCs against hypoxia and excitotoxicity in cell culture.
In this culture, the glial cell monolayer express immunocytochemically nerve growth factor (NGF) and brain-derived neuritrophic factor (BDNF), vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), transforming growth factor β1 (TGF β1).
The ciliary marginal zone (CMZ) of the vertebrate retina contains undifferentiated progenitor cells that continue to proliferate and differentiate into retinal-specific cell types. With this culture system, cells from the CMZ of neonatal rat retina identified as various retinal cell types. To investigate whether conditioned medium with NGF and BDNF can induce differentiation of the cells from the CMZ, however, cells cultured in the conditioned medium showed very little retinal cell differentiation.

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 小関 義之: 東京女子医科大学雑誌. 71. 297-303 (200*)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yoshiyuki Koseki: "The protective effect of a nitric oxide synthase inhibitor in rat cultured retinal ganglion cells."Journal of Tokyo Women's Medical University. 71. 297-303 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] 小関 義之: "ラット培養網膜神経節細胞における一酸化窒素合成酵素阻害剤の細胞保護効果"東京女子医科大学雑誌. 71巻5・6. 297-303 (2001)

    • Related Report
      2001 Annual Research Report

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Published: 2001-04-01   Modified: 2016-04-21  

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