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Preparation and analysis of model mice with Parkinson's disease

Research Project

Project/Area Number 11670654
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Neurology
Research InstitutionTokyo Metropolitan Institute of Gerontology

Principal Investigator

TAKAHASHI Mayumi  Tokyo Metropolitan Institute of Gerontology, Department of Ultrastructure, Assistant, 超微形態部門, 研究助手 (50133632)

Co-Investigator(Kenkyū-buntansha) 白澤 卓二  財団法人 東京都老人総合研究所, 分子遺伝学部門, 室長 (80226323)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1999: ¥1,800,000 (Direct Cost: ¥1,800,000)
KeywordsParkinson's disease / Model mouse / Dopaminergic neuron / Superoxide / Mn-SOD / Knockout mouse / Gene therapy / Adeno virus / ドーパミン / 人口高齢化 / ES細胞 / Tyrosine Hydroxylase
Research Abstract

The generation of Parkinson's disease model mouse Reactive Oxygen Species (ROS) plays a pathological role in the development of neurodegenerative diseases including Parkinson's disease. Doperminergic system in CNS participates in the higher brains functions such as recognition, motor coordination, and memory. Neuropathologically, the doperminergic neurons are vulnerable for the ageing process of the brain where the apoptotic figures are often observed in the midbrain of aged animal brains. Clinically, the reduction in the number of doperminergic neurons leads to the symptom of Parkinson's disease such as tremor, rigidity, and motor disturbance. To address the pathogenic mechanisms of Parkinson's disease in aged population, we tried to generate a model mouse in which Mn-SOD gene, a defensive enzyme against ROS, is conditionally knocked down specifically in doperminergic neurons. For this purpose, we first generated the Mn-SOD flox mouse in which recombination signal called loxp is inserted in the genomic locus of mouse Mn-SOD gene to delete the catalytic exons by cre recombinase. By crossing with TH-Cre transgenic mice (provided by Prof. Kobayashi, Fukushima) which specifically express cre recombinase in dopaminergic neurons, Mn-SOD flox mice would inactivate Mn-SOD gene in doperminergic neurons and provide an excellent model system for Parkinson's disease.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (15 results)

All Other

All Publications (15 results)

  • [Publications] Shimizu,T. et al.: "Isoaspartate formation and neurodegeneration in Alzheimer's disease."Archives of Biochemistry and Biophysics. 381. 225-234 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Nakano,H. et al.: "Targeted disruption of traf5 gene causes defects in CD40-and CD27-mediated lymphocyte activation."Proc Natl Acad Sci USA. 96. 9803-9808 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tomoda,T. et al.: "A mouse serine/threonine kinase homologous to Gelegans UNC51 functions in parallel fiber formation of cerebellar granule neurons."Neuron. 24. 833-846 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shimizu, T., Watanabe, A., Ogawara, M., Mori, H., and Shirasawa, T.: "Isoaspartate formation and neurodegeneration in Alzheimer's disease."Arch. Biochem. Biophys.. 381. 225-234 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Nakano, H., Sakon, S., Koseki, H., Takemori, T., Tada, K., Matsumoto, M., Munechika, E.Sakai, T., Shirasawa, T., Akiba, H., Kobata, T., Santee, S.M., Ware, C.F., Rennert, P.D., Taniguchi, M., Yagita, H., and Okumura, K.: "Targeted disruption of traf5 gene causes defects in CD40- and CD27- mediated lymphocyte activation."Proc. Natl. Acad. Sci. USA. 96. 9803-9808 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tomoda, T., Bhatt, R.S., Kuroyanagi, H., Shirasawa, T., and Hatten, M.E.: "A mouse serine threonine kinase homologous to C.elegans UNIC51 functions in parallel fiber formation of cerebellar granule neurons."Neuron. 24. 833-846 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shimizu,T. et al.: "Isoaspartate formation and neurodegeneration in Alzheimer's disease."Archives of Biochemistry and Biophysics. 381. 225-234 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Nakano,H. et al.: "Targeted disruption of traf5 gene causes defects in CD40- and CD27- mediated lymphocyte activation."Proc Natl Acad Sci USA. 96. 9803-9808 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tomoda,T. et al.: "A mouse serine/threonine kinase homologous to C. elegans UNC51 functions in parallel fiber formation of cerebellar granule neurons."Neuron. 24. 833-846 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tomoda T. et al.: "A mouse serine/threonine kinase homologous to C.elegans UNC51 functions in parallel fiber formation of cerebellar granule neurons"Neuron. 24. 833-846 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Nakano H. et al.: "Targeted disruption of traf5 gene causes defects in CD40- and CD27-mediated lymphoeyte activation"Proc Natl Acad Sci USA. 96. 9803-9808 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Yan J. et al.: "Mouse ULK2, a novel member of the UNC-51-like protein kinases.unique features of functional domains"Oncogene. 18. 5850-5859 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Fukuda H. et al.: "Synthesis, Aggregation, and Neurotoxicity of the Alzheimer's A beta 1-42 Amyloid Peptide and Its Isoaspartyl Isomers"Bioorganic & Medicinal Chemistry Letters. 9. 953-956 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Yamamoto A. et al.: "Deficiency in protein L-isoaspartyl methyltransferase results in a fatal progressive epilepsy"J Neurosci. 18. 2063-2074 (1998)

    • Related Report
      1999 Annual Research Report
  • [Publications] Smith C. D. et al.: "Crystallization and preliminary cryogenic X-ray diffraction analyses of protein L-isoaspartyl O-methyltransferase from human fetal brain"Proteins. 28. 457-460 (1997)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2025-11-20  

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