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Functional significance of Schwann cell-derived factors during periphralnerve regeneration

Research Project

Project/Area Number 09671493
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthopaedic surgery
Research InstitutionOsaka University Faculty of Medicine

Principal Investigator

YONENOBU Kazuo  Osaka University Faculty of Medicine, Associate professor, 医学部, 助教授 (50127320)

Co-Investigator(Kenkyū-buntansha) SHIMADA Kozo  Osaka University Faculty of Medicine, Assistant professor, 医学部, 助手 (00216061)
WADA Eiji  Osaka University Faculty of Medicine, Assistant professor, 医学部, 助手 (40273643)
ARAKI Toshiyuki  Osaka University Faculty of Medicine, Assistant professor, 医学部, 助手 (70263275)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1998: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1997: ¥1,200,000 (Direct Cost: ¥1,200,000)
Keywordsperipheral nerve / nerve regeneration / Schwann cell / adhesion / ninjurin
Research Abstract

During peripheral nerve regeneration, Schwann cells generate a number of factors which are necessary for nerve regeneration, which is a distinctive characteristics of peripheral nervous system.We have found plasma membrane proteins, ninjurin-1, by virtue of its up-regulation in Schwann cells after nerve injury, and ninjurin-2 by its homology with ninjurin1.Ninjurin-2 expression in the normal adult organs was primarily found in hematopoietic and lymphatic organs.In the peripheral nervous system, ninjurin-2 expression was found mostly in neurons of the peripheral ganglia including dorsal root and trigeminal ganglia, which showed a good contrast to ninjurin-1 exression observed only in satellite cells.After peripheral nerve injury, ninjurin-1 and -2 are both up-regulated in the neurons 1-3 days after injury.In the Schwann cells, both ninjurin-1 and -2 are hardly expressed in the normal myelinating Schwann cells, and dramatically up-regulated after nerve injury.Furthermore, we have found that neurite outgrowth from primary cultured DRG neurons is promoted when they are grown on ninjurin-2-overexpressing CHO cells.These results indicate that ninjurin-2 may functions differently from ninjurin-1 in normal peripheral nervous system, but after injury both ninjurin1 and ninjurin-2 promote nerve regeneration by their homophilic adhesion properties.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Araki T,Zimonjic DB,Popescu Milbrandt J: "Mechanism of homophilic binding mediated by ninjurin,a novel widely expressed adhesion molecule." J.Biol.Chem. 272. 21373-21380 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Araki T,Zimonjic DB,Popescu NC,Milbrandt J: "Mechanism of homophilic binding mediated by ninjurin, a novel widely expressed adhesion molecule." J.Biol.Chem.272. 21373-21380 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Araki,T: "Mechanism of homophilic binding mediated by ninjurin,a novel widely expressed adhesion molecule." J.Biol.Chem.272. 21373-21380 (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2017-10-12  

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