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2002 Fiscal Year Final Research Report Summary

グリア細胞によるイオンチャンネルの発現と局在の調節機構

Research Project

Project/Area Number 10214204
Research Category

Grant-in-Aid for Scientific Research on Priority Areas

Allocation TypeSingle-year Grants
Review Section Biological Sciences
Research InstitutionNational Institute for Physiological Sciences

Principal Investigator

IKENAKA Kazuhiro  Okazaki National Institutes, National Institute for Physiological Sciences, Professor, 生理学研究所, 教授 (00144527)

Co-Investigator(Kenkyū-buntansha) BABA Hiroko  Tokyo University of Pharmacology and Life Science, Professor, 薬学部, 教授 (40271499)
FUJIMOTO Ichiro  Center for Integrative Biochemistry, Research Associate, 統合バイオサイエンスセンター, 助手 (70264710)
KAGAWA Tetsushi  National Institute for Physiological Sciences, Research Associate, 生理学研究所, 助手 (50270484)
Project Period (FY) 1998 – 2001
Keywordsmyelinated fiber / ion channel clustering / Node of Ranvier / paranode
Research Abstract

Recently it has been shown that the function of oligodendrocyte (OL) is not only to insulate the axons but also to direct ion channel clustering on the axonal surface. In this study we identified the molecules involved in the interaction between OL and axon, and investigated the mechanisms underlying the induction of ion channel clustering.
1) Differentiation and maturation of OLs are regulated by signals derived from the axons. One of the signals known is Jagged-Notch signaling. We identified that expression of Mash1, a transcriptional factor, is suppressed by the activation of this signaling. We also found that development of OL is abnormal in the Mash1 knock-out mouse indicating that Mash1 is playing an important role in OL development in vivo.
2) We found that the presence of myelin membrane is not required in the initial clustering of the voltage gated sodium channels, but is required for the maturation of the nodes. On the other hand the myelin membrane and paranodal junctions are essential for the potassium channels to cluster at proper sites. Moreover, they are also necessary for the maintenance of the clusters. We also found that sulfatide and CD9 play important roles in transporting molecules, such as NF155, that are essential for the paranodal junction formation to the paranodes.

  • Research Products

    (35 results)

All Other

All Publications (35 results)

  • [Publications] Ishibashi, T.: "Initiation of sodium channel clustering at the node of Ranvier in the mouse optic nerve"Neurochem. Res.. 28. 117-125 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishibashi, T.: "A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation"J. Neurosci.. 22. 6507-6514 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takebayashi, H.: "The basic helix-loop-helix factor Olig2 is essential for development of motoneuron and oligodendrocyte lineages"Current Biology. 12. 1157-1163 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamada, M.: "Mutant PLP/DM20 cannot be processed to secrete PLP-related oligodendrocyte differentiation/survival factor"Neurochem. Res.. 26. 639-645 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Wada, T.: "Dorsal spinal cord inhibits oligodendrocyte development"Dev. Biol.. 227. 42-55 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shibata, R.: "A-type K^+ current mediated by the Kv4 channel regulates the generation of action potential in developing cerebellar granule cells"J. Neurosci.. 20. 4145-4155 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Baba, H.: "Completion of myelin compaction, but not the attachment of oligodendroglial processes triggers K^+ channel clustering"J. Neurosci. Res.. 58. 752-764 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamada, M.: "Proteolipid protein gene product can be secreted and exhibit biological activity during early development"J. Neurosci.. 19. 2143-2151 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shibata, R.: "Expression of Kv3.1 and Kv4.2 genes in developing cerebellar granule cells"Dev. Neurosci.. 21. 87-93 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yonemasu, T.: "Proximal promoter region is sufficient to regulate tissue-specific expression of UDP-galactose : Ceramide galactosyltransferase gene"J. Neurosci. Res.. 52. 757-765 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Miyamura, T.: "Metabolic labeling of a subset of glial cells by UDP-galactose : Implication for astrocyte lineage diversity"J. Neurosci. Res.. 52. 173-183 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yoshimatsu, T.: "Improvement of retroviral packaging cell lines by introducing the polyomavirus early region"Human Gene Therapy. 9. 161-172 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 中平英子: "神経研究の進歩"医学書院. 9 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 鹿川哲史: "分子細胞治療"先端医学社. 6 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 長谷川明子: "実験医学"羊土社. 9 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 鹿川哲史: "脳の科学"星和書店. 5 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 池中一裕: "組織培養工学"ニュー・サイエンス社. 4 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 和田圭樹: "CLINICAL NEUROSCIENCE"中外医学社. 4 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 南木浩二: "脳21"金芳堂. 15 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 馬場広子: "遺伝子治療開発研究ハンドブック"エヌ・ティー・エス. 6 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 岩崎靖乃: "遺伝子医学"(株)メディカルドゥ. 5 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 池中一裕: "NEUROLOGICAL SURGERY"医学書院. 5 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 中平健祐: "脳の科学"星和書店. 7 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishibashi, T., Ikenaka, K., Shimizu, T., Kagawa, T, and Baba, H.: "Initiation of sodium channel clustering at the node of Ranvier in the mouse optic nerve"Neurochem. Res.. 28. 117-125 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishibashi, T., Dupree, J.L., Ikenaka, K., Hirahara, Y., Honke, K., Peles, E., Popko, B., Suzuki, K., Nishino, H., Baba, H.: "A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation"J. Neurosci.. 22. 6507-6514 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takebayashi, H., Nabeshima, Y., Yoshida, S., Chisaka, O., Ikenaka, K., Nabeshima, Y.: "The basic helix-loop-helix factor Olig2 is essential for development of motoneuron and oligodendrocyte lineages"Current Biology. 12(13). 1157-1163 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamada, M., Jung, M., Kagawa, T., Ivanova, A., Nave, K.-A., and Ikenaka, K.: "Mutant PLP/DM20 cannot be processed to secrete PLP-related oligodendrocyte differentiation/survival factor"Neurochem. Res.. 26. 639-645 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Wada, T., Kagawa, T., Ivanova, A., Zalc, B., Shirasaki, R., Murakami, F., Iemura, S., Ueno, N., and Ikenaka, K.: "Dorsal spinal cord inhibits oligodendrocyte development"Dev. Biol.. 227. 42-55 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shibata, R., Nakahira, K., Shibasaki, K., Wakazono, Y., Imoto, K., and Ikenaka, K.: "A-type K^+ current mediated by the Kv4 channel regulates the generation of action potential in developing cerebellar granule cells"J. Neurosci.. 20. 4145-4155 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Baba, H., Akita, H., Ishibashi, T., Inoue, Y., Nakahira, K., and Ikenaka, K.: "Completion of myelin compaction, but not the attachment of oligodendroglial processes triggers K^+ channel clustering"J. Neurosci. Res.. 58. 752-764 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamada, M., Ivanova, A., Yamaguchi, Y., Less, M.B., and Ikenaka, K.: "Proteolipid protein gene product can be secreted and exhibit biological activity during early development"J. Neurosci.. 19(6). 2143-2151 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shibata, R., Wakazono, Y., Nakahira, K., Trimmer, J.S., and Ikenaka, K.: "Expression of Kv3.1 and Kv4.2 genes in developing cerebellar granule cells"Dev. Neurosci.. 21. 87-93 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yonemasu, T., Nakahira, K., Okumura, S., Kagawa, T., Espinosa de los Monteros, A., de Vellis, J., and Ikenaka, K.: "Proximal promoter region is sufficient to regulate tissue-specific expression of UDP-galactose : Ceramide galactosyltransferase gene"J. Neurosci. Res.. 52. 757-765 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Miyamura, T., Morita, N., Baba, H., Hase, S., Kajimoto,T., Tsuji, S., Kawata, M., Kato, I., Mikoshiba, K., and Ikenaka, K.: "Metabolic labeling of a subset of glial cells by UDP-galactose : Implication for astrocyte lineage diversity"J. Neurosci. Res.. 52. 173-183 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yoshimatsu, T., Tamura, M., Kuriyama, S., and Ikenaka, K.: "Improvement of retroviral packaging cell lines by introducing the polyomavirus early region"Human Gene Therapy. 9. 161-172 (1998)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2004-04-14  

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