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Analysis on novel regulatory proteins attached to the growth cone vesicles.

Research Project

Project/Area Number 09680758
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Neurochemistry/Neuropharmacology
Research InstitutionGunma University

Principal Investigator

IGARASHI Michihiro  Gunma University School of Medicine, Assistant, 医学部, 助手 (50193173)

Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 1998: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 1997: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsgrowth cone / SNARE complex / syntaxin / synapse / rab3A / rabphilin / exocytosis / シナプス終末 / テトロトキシン / Rab3A サイクリング / GAP-43 / 開口放出 / シナプス前終末 / C-キナーゼ / カルパイン
Research Abstract

1) Growth cones are considered as the precursor of presynaptic terminals. To elucidate the minimal requirement of exocytotic molecular machinery, we examined the characteristics of exocytosis in growth cones using alpha-latrotoxin (alpha-LTX). The major biochemical difference between the adult presynptic terminal (SPS) and the isolated growth cone (IGC) was that rab3A was converted to GTP-form in the former, but remained GDP-form in the latter. We found that rabphilin was localized in much smaller amounts in IGC than in SPS.Following a supply of rabphilin, the IGC obtained as highly alpha-LTX-sensitivity as SPS, and the GDP-GTP conversion attached to rab3A on the GCV.In native IGCs, the GCVs had the SNAREs but riot NSF and alpha- SNAP ; while in the rabphilin-supplied IGC, the GCVs recruited NSF and alpha-SNAP, and the SNARE-NSF-SNAP complex was formed on the GCVs. Our results suggest that rab3A cycling develops later than the SNARE by accumulation of rabphilin, and that it is involved in determining the efficiency of exocytosis forced by alpha-LTX.
2) Although growth cones responds to various modulators of neurite outgrowth, the signal-transducing mechanisms for these modulators in growth cones are unclear. I examined L-type VSCC-dependent signaling p-athways. In intact IGCs, Bay K 8644 (BK) induced much more rapid elevation of [Ca^<2+>] than that in SPS.Ca^<2+>-dependent phosphorylation of GAP-43 and MAROKS protein by protein kinase C (PKC) was enhanced in the JGC by BK, resulting in the release of these proteins from the membrane, which is consistent with our recent report. In addition, the Ca^<2+>-dependent degradation of brain spectrin by calpain was also enhanced by BK or GABA, consequently inducing the release of alpha-actinin from the membrane skeleton of growth cones. The activities of PKC and calpain were not inhibited by inhibitors of the other.

Report

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

    (19 results)

All Other

All Publications (19 results)

  • [Publications] Ohbayasi K.et al.: "Shimulation of L-type Ca^<2+> channels in growd cored activated two independent signaling natuways." J.Neurosci.Res.51(6). 682-696 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 五十嵐道弘: "成長円錐からシナプス終末への転換の分子機構" 蛋白質核酸酵素. 印刷中. (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 五十嵐道弘: "軸索成長に関与する情報伝達" 生体の科学. 48(6). 542-554 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 五十嵐道弘: "軸索成長の分子機構" 医学のあゆみ. 180(2). 138-140 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi, M. et al.: "The SNARE Complex in groulk cored" J.Neenotei.17(4). 1460-1470 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi, M. (共著) <Fujosawa, H de.>: "Molecular Mechanism of Axon Growth and Nerve Pattern Formation" Japan Scientific Societies Press/Karger, Tokyo/Badel, 280(107-120) (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Ohbayashi K,Fukura H,Inoue HK,Komiya Y,Igarashi M: "Stimulation of L-type Ca^<2+> channel in growth cones activates two independent singling pathways" J.Neurosci.Res.51(6). 682-696 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi M,Tagaya M,Komiya Y: "The soluble N-ethylmaleimide-sensitive factor attachment protein receptor(SNARE) complex in growth cones : molecular aspects of the axon terminal development." J.Neurosci.17(4). 1460-1470 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi M: "From growth cone to synpase." Tanapkusitu-Kakusan-Koso(in Japanese). (in press). (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi M: "Signaling pathways involved in axonal growth." Seitai-no-Kagaku. 48(6). 542-554 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi M: "Molecular mechanisms of axonal growth." Igaku-no-Ayumi. 180(2). 138-140 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Igarashi M.: Japan Scientific Societies Press/Karge, Tokyo/Basel. Significance of the SNARE mechanisms in growth cones.Molecular Mechanisms of Axon Growth and Nerve Pattern Formation(Fujisawa H,ed.), 107-120 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Ohbayashi K et al.: "L-tipe Ca^<2+> Sfimulation in grouth cones activates two independent Cignaling pathways." Journal of Neuroxience Research. 5/(6). 682-696 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 五十嵐道弘: "成長円錐からシナプス終末への変化過程の分子機構" 蛋白質 核酸 酵素. 44(印刷中). (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] Igarashi,M.Tagaya M.Kamiya Y: "The SNARE Corplex in grouth cenes" Journal of Neuroscience. 17(4). 1460-1470 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Ohbayashi K, Fukura H.Inoue HK.Kamiya Y, Igarashi M: "Stimulatotn of L-tyne Ca^<2+> channel in grocuth cones activates two tdependent pathways" Journal of Neuroscience Research(印刷中). (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] 五十嵐道弘: "軸索成長の分子機構" 医学のあゆみ. 180(6). 138-140 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 五十嵐道弘: "軸索成長の制御に関与する情報伝達系" 生体の化学. 48(6). 542-554 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Igarashi M (他21名)(Fujisawa H ed): "Mechanisms of axonal groauth and newe patteun formation" Kargen/Japan Scientific Societies Press, 280 (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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