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Therapy for neurodegeneerative disease using novel screening method for chemical chaperon.

Research Project

Project/Area Number 18590967
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Neurology
Research InstitutionKanagawa Cancer Center Research Institute

Principal Investigator

OSAKA Hitoshi  Kanagawa Cancer Center Research Institute, Kanagawa Center Research Institute, 技幹 (90426320)

Co-Investigator(Kenkyū-buntansha) INOUE Ken  National Institute of Neuroscience, 神経研究所・疾病研究第二部, 室長 (30392418)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,190,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥390,000)
Fiscal Year 2007: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2006: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsBiological neurochemistry / Neurodegeneration / Chaperon / 小胞体ストレス
Research Abstract

(1)Therapy for Pelizaeus-Merzbacher with chaperon. We failed to establish the gas-chromatographically measurement for a candidate chemical. We switched to search for chemicals to decrease the expression level of proteolipid protein(PLP). Duplication of PLP accounts for the half of the PMD patients. In C6 glioma cell line expressing PLP, we could measure PLP mRNA level by Quantitative RT-PCR. PLP expression was normalized by that of hypoxanthine guanine phosphoribosyl transferase. At first, we found that the more cell differentiate, the more PLP expresses. We optimized screening condition as follows ; chemicals extracted from food were added at final concentration of 10μM at cell density of 2.5×10^5/well(9.2cm^2) for 48hrs with DMEM(low glucose) including 1%fetal bovine serum. We screened the library including more than one hundred of food chemicals. We found 2 chemicals that decrease the PLP mRNA expression more than 50%. 11 chemicals were found to decrease the PLP expression level mor … More e than 30%. We have already found that PLP missence mutations cause overload to proteorytic system in the cell leading to cell death. Therefore, food chemicals that lower the level of PLP may be applied to the PMD patients with duplication as well as missence mutations in PLP gene.
(2)Establishment of therapeutic effect in mouse model of PMD. For proper evaluation of drugs for PMD, we need to assess the degree of myelination in mouse model. We tried to quantitatively measure myelination by microscopic examinations. Firstly, we evaluated the degree of myelination using light microscopic examinations after conventional HE, Kluver-Barrera's or immune staining using the antibodies to PLP and myelin basic protein. These methods partially disclosed the dysmyelination of PMD model mouse. Electron microscopic examination revealed the degree of myelination properly. Optical nerve was superior for quantitative examination among central nervous system, as it contained the uniform numbers of neuron and oligodendrocytes. Less

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (32 results)

All 2008 2007 2006

All Journal Article (23 results) (of which Peer Reviewed: 8 results) Presentation (7 results) Book (2 results)

  • [Journal Article] DISTINCT CLINICAL COURSE OF EPILEPSY WITH AN SCN2A MUTATION-COMPARISON WITH SCN1A MUTATIONS2008

    • Author(s)
      Osaka, H., Mazaki, E., Okamura, N., Iai, M., Yamada, M., Yamakawa, K., Yamashita, S.
    • Journal Title

      Progress in Epileptic Disorders

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter2008

    • Author(s)
      Tohyama, J., Akasaka, N., Osaka, H.Maegaki, Y., Kato, M., Saito, N.Yamashita, S., Ohno, K.
    • Journal Title

      Brain Development 30

    • NAID

      10025576951

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] De novo mutations in the gene encoding STXBP1(MUNC18-1)cause early infantile epileptic encephalopathy2008

    • Author(s)
      Saitsu, H., Kato, M., Mizuguchi, T., Hamada, K., Osaka, H., Tohyama, J., Uruno, K., Kumada, S., Nishiyama, K., Nishimura, A., Okada, I., Yoshimura, Y., Hirai, S., Kumada, T., Hayasaka, K., Fukuda, A., Ogata, K., Matsumoto, N
    • Journal Title

      Nature Genetics

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] De novo mutations in the gene encoding STXBP1(MUNC18-1) cause early infantile epileptic encephalopathy2008

    • Author(s)
      Saitsu H, Kato M, Mizuguchi T, Hamada K, Osaka H, Tohyama J, Uruno K, Kumada S, Nishiyama K, Nishimura A, Okada I, Yoshimura Y, Hirai S, Kumada T, Hayasaka K, Fukuda A, Ogata K & Matsumoto N
    • Journal Title

      Nature Genetics 40

      Pages: 782-788

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Pelizaeus-Merzbacher Disease2008

    • Author(s)
      Osaka H.
    • Journal Title

      Diagnostic pediatric neuroradiology, (Tokyo igaku-sha)

      Pages: 484-485

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Distinct clinical course of SMEI with SCN 2A mutation-Comparison with SCN 1A mutations.2008

    • Author(s)
      Osaka H, Mazaki E Ohamura N, Mizue I, Yamada M, Yamakawa K Yamashita S.
    • Journal Title

      Biology of Seizure Susceptibility in Developing Brain. Editions John Libbey Eurotext

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] DISTINCT CLINICAL COURSE OF EPILEPSY WITH AN SCN2A MUTATION-COMPARISON WITH SCN1A MUTATIONS2008

    • Author(s)
      Osaka, H., Mazaki, E., Okamura, N., Iai, M., Yamada, M., Yamakawa, K., Yamashita, S.
    • Journal Title

      Progress in Epileptic Disorders (in print)

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter2008

    • Author(s)
      Tohyama, J., Akasaka, N., Osaka, H., Maegaki, Y., Kato, M., Saito, N., Yamashita, S., Ohno, K.
    • Journal Title

      Brain Development 30

      Pages: 349-355

    • NAID

      10025576951

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] De novo mutations in the gene encoding STXBP1(MUNC18-1) cause early infantile epileptic encephalopathy2008

    • Author(s)
      Saitsu, H., Kato, M., Mizuguchi, T., Hamada, K., Osaka, H., Tohyama, J., Uruno, K., Kumada, S., Nishiyama, K., Nishimura, A., Okada, I., Yoshimura, Y., Hirai, S., Kumada, T., Hayasaka, K., Fukuda, A., Ogata, K., Matsumoto, N
    • Journal Title

      Nature Genetics (in print)

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation2007

    • Author(s)
      Osaka, H., Ogiwara, I., Mazaki, E., Okamura, N., Yamashita, S., Imai, M., Yamada, M., Kurosawa, K., Iwamoto, H., Yasui-Furukori, N., Kaneko, S., Fujiwara, T., Inoue, Y., Yamakawa, K
    • Journal Title

      Epilepsy Research 75

      Pages: 46-51

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Dopaminergic neuronal loss in transgenic mice expressing the Parkinson's disease-associated UCH-L1 I93M mutant.2007

    • Author(s)
      Setsuie R, Wang YL, Mochizuki H, Osaka H, Hayakawa H, Ichihara N, et. al.
    • Journal Title

      Neurochem Int 50

      Pages: 119-2

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter.2007

    • Author(s)
      Tohyama J, Akasaka N, Osaka H, Maegaki Y, Kato M, Saito N, et. al.
    • Journal Title

      Brain Dev. Dec 5(Epub ahead of print)

    • NAID

      10025576951

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Patients with sodium channel alpha 1 gene mutation show wide phenotypic variation2007

    • Author(s)
      Osaka, H., Ogiwara, I., Mazaki, E., Okamura, N., Yamashita, S., Iai, M., Yamada, M., Kurosawa, K., Iwamoto, H., Yasui-Furukori, N., Kanneko, S., Fujiwara, T., Inoue, Y., Yamakawa, K
    • Journal Title

      Epilepsy Research 75

      Pages: 46-51

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Aberrant trafficking of a proteolipid protein in a mild Pelizaeus-Merzbacher disease.2006

    • Author(s)
      Koizume, S., Takizawa, S., Fujita, K., Aida, N., Yamashita, S., Miyagi, Y., and Osaka, H.
    • Journal Title

      Neuroscience 141

      Pages: 1861-1869

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Parkin potentiates ATP-indused currents due to activation of P2X receptors in PC12 cells.2006

    • Author(s)
      Sato, A., Arimura, Y., Manago, Y., Nishikawa, K., Aoki, K., Wada, E., Suzuki, Y., Osaka, H., Setsuie, R., et. al.
    • Journal Title

      J Cell Physiol. 209

      Pages: 172-82

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Overexpression of ubiqitin carboxyl-terminal hydrolase L1 arrests spermatogenesis in transgenic mice.2006

    • Author(s)
      Wang, Y. L., Liu, W., Sun, Y J., Kwon, J., Setsuie, R., Osaka, H., Noda, M., Aoki, S., Yoshikawa, Y., and Wada, K.
    • Journal Title

      Mol Reprod Dev 73

      Pages: 40-49

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Taccination and infection as causative factors in Japanese patients with Rasmussen syndrome : Molecular mimicry and HLA class I2006

    • Author(s)
      Takahashi, Y, Matsuda, K, Kubota Y, Shimomura J, Yamasaki, E, Kudo, T, Fukushima K, Osaka H, Akasaka N, Imamaura A, Yamada S, Kondo, N, Fujiwara
    • Journal Title

      Clinical & Developmental Immunology 13

      Pages: 381-38

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Aberrant trafficking of a proteolipid protein in a mild Pelizaeus-Merzbacher disease.2006

    • Author(s)
      Koizume, S., Takizawa, S., Fujita, K., Aida, N., Yamashita, S., Miyagi, Y., Osaka, H.
    • Journal Title

      Neuroscience 141

      Pages: 1861-1869

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Parkin potentiates ATP-induced currents due to activation of P2X receptors in PC12 cells.2006

    • Author(s)
      Sato, A., Arimura, Y., Manago, Y., Nishikawa, K., Aoki, K., Wada, E., Suzuki, Y., Osaka, H., Setsuie, R., Sakurai, M.
    • Journal Title

      J Cell Physiol.

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Dopaminergic neurona1 loss in transgenic mice expressing the Parkinson' s disease-associated UCH-LI I93M mutant.2006

    • Author(s)
      Setsuie, R., Wang, Y.L., Mochizuki, H., Osaka, H., Hayakawa, H., Ichihara, N., Li, H., Furuta, A., Sano, Y., Sun, Y.J., et al.
    • Journal Title

      Neurochem Int. 50

      Pages: 119-129

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Solo/Trio8, a membrane-associated short isoform of Trio, modulates endosome dynamics and neurite elongation.2006

    • Author(s)
      Sun, Y.J., Nishikawa, K., Yuda, H., Wang, Y.L., Osaka, H., Fukazawa, N., Naito, A., Kudo, Y., Wada, K., Aoki, S.
    • Journal Title

      Mol Cell Biol 26

      Pages: 6923-6935

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Overexpression of ubiquitin carboxy1-terminal hydrolase L1 arrests spermatogenesis in transgenic mice.2006

    • Author(s)
      Wang, Y.L., Liu, W., Sun, Y.J., Kwon, J., Setsuie, R., Osaka, H., Noda, M., Aoki, S., Yoshikawa, Y., Wada, K.
    • Journal Title

      Mol Reprod Dev 73

      Pages: 40-49

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Vaccination and infection as causative factors in Japanese patients with Rasmussen syndrome : Molecular mimicry and HLA class I2006

    • Author(s)
      Takahashi, Y, Matsuda, K, Kubota Y, Shimomura J, Yamasaki, E, Kudo, T, Fukushima K, Osaka H, Akasaka N, Imamaura, A, Yamada, S, Rondo, N, Fujiwara, T
    • Journal Title

      Clinical & Developmental Irnmunology 13

      Pages: 381-387

    • Related Report
      2006 Annual Research Report
  • [Presentation] Establishment of screening system for Pelizaeus-Merzbacher disease2008

    • Author(s)
      Osaka H, Kenji K, Mizue I, Michiko Y, Yamashita J.
    • Organizer
      50th Annual Meeting of Japanese pediatric neurology
    • Place of Presentation
      Tokyo
    • Year and Date
      2008-05-28
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Pelizaeus-Merzbacher病の病態に基づく治療法開発の試み(共同演者)2007

    • Author(s)
      井上 健, 他
    • Organizer
      第51回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2007-09-13
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Annual Research Report 2007 Final Research Report Summary
  • [Presentation] Distinct clinical course of SMEI with SCN 2A mutation-Comparison with SCN 1A mutations.2007

    • Author(s)
      Osaka H, Mazaki E, Okamura N, Yamashita S, Mizue I, Yamada M and Yamakawa K
    • Organizer
      10th Annual Meeting of the Infantile Seizure Society ; INTERNATIONAL SYMPOSIUM ON BIOLOGY OF SEIZURE SUSCEPTIBILITY
    • Place of Presentation
      Tokyo
    • Year and Date
      2007-04-07
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Pelizaeus-Merzbacher病の病態解析2007

    • Author(s)
      小坂 仁, 他
    • Organizer
      49回日本小児神経学会総会
    • Place of Presentation
      大阪
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Annual Research Report 2007 Final Research Report Summary
  • [Presentation] Pathophysiology for Pelizaeus-Merzbacher disease2007

    • Author(s)
      Osaka H, Kenji K, Mizue I, Michiko Y, Yamashita J.
    • Organizer
      49th Annual Meeting of Japanese pediatric neurology
    • Place of Presentation
      Osaka
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Special Lecture ; Clinical, pathophysiology and the therapy for dysmyelinating disease2006

    • Author(s)
      Osaka H.
    • Organizer
      14th Shinshu neuro-pediatric conference
    • Place of Presentation
      Matsumoto
    • Year and Date
      2006-05-13
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Aberrant trafficking of a mutated proteolipid protein in a mild Pelizaeus-Merzbacher disease.2006

    • Author(s)
      Koizume S, Takizawa S, Yamashita S, Miyagi Y, OsakaH
    • Organizer
      29th Annual Meeting of Japanese molecular biology
    • Place of Presentation
      Kyoto
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Book] elizaeus-Merzbacher病; 小児中枢神経疾患の画像診断20082008

    • Author(s)
      小坂 仁
    • Total Pages
      2
    • Publisher
      東京医学社
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Book] elizaeus-Merzbacher病;小児中枢神経疾患の画像診断20082008

    • Author(s)
      小坂 仁
    • Total Pages
      2
    • Publisher
      東京医学社
    • Related Report
      2007 Annual Research Report

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Published: 2006-04-01   Modified: 2016-04-21  

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