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Molecular pathological study of hereditary spinocerebellar ataxia.

Research Project

Project/Area Number 09670642
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Neurology
Research InstitutionThe University of Tokyo

Principal Investigator

MURAYAMA Shigou  The University of Tokyo Hospital, Neurology Research Lecture, 医学部・附属病院, 助手 (50183653)

Co-Investigator(Kenkyū-buntansha) HIMURO Kimihide  The University of Tokyo Hospital, Neurology Fellow, 医学部・附属病院, 医員
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1998: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1997: ¥2,100,000 (Direct Cost: ¥2,100,000)
Keywordsspinocerebellar ataxia / molecular pathology / CAG repeat / Machedo-Joseph disease / DRPLA / in situ hybridization / 遺伝性脊髄小脳変性症 / 分子病理 / 免疫組織化学 / インシチュ-ハイブリダイゼーション / CAG リピート病 / マカドジョセフ病 / 画像解析
Research Abstract

1. In situ hybridization
Seventeen-day-old fetus and neonate rats were served for in situ hybridization study. A 35S-labeled c-RNA probe from MJD-1 was synthesized as was previously described (Nishiyama et al, Ann Neurol 1997). Sagittally sliced whole bodies of rats were snap-frozen and processed for in situ hybridization. However, no significant signal was obtained.
2. Genotype-phenotype correlation
Eight cases of genetically-determined Machado-Joseph disease (MJD) were studied morphologically. The case number, age, sex and the size of normal and expanded alleles were as follows : #1, 77year-old male, 23/64 ; #2, 78yea-old female, 21/69 ; #3, 44year-old male, 25/75 ; #4, 62year-old female, 14/76 ; #5, 46year-old male, 29/77 ; #6, 49 year-old male, 14/77 ; #7,44 year-old male, 23/79 ; #8, 32 year-old male, 19/79. Ubiquitin immunocytochmistry was applied to all the sections of the central nervous system, in order to elucidate the presence of intranuclear neuronal inclusions. α B-crystallin … More e immunocytochemistry was applied to the sections including subthalmic nucleus and the density of the immunoreactive oligodendroglia was calculated. Intranuclear inclusions were seen in very small number of pontine neurons and showed no correlation with the length of the expanded alleles. In contrast, the density of oligodendroglia was definitely increased, compared with normal controls. The density calculated by age showed correlation with the length of the expanded allele. This finding statistically resembled the decrease of neurons in the striatum in Huntington's disease and could represent the core pathology of MJD.
3. Comparative pathological study of Haw-River syndrome (HRS) and DRPLA
Two cases of HRS and six cases of DRPLA were pathologically studied. Both showed prominent grumosus alteration in the dentate nuclei and pallido-luysian degeneration. Axonal spheroids emphasized in HRS were also seen in some cases of DRPLA. Thus, these two cases were essentially the same and the name of HRS may only represent geographical cluster. Less

Report

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

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Murayama S et al.: "Regional and cellular expression of the D*t*t*-pallidolecysian atrophy"Annals of Neurology. 41. 599-605 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Murayama S et al.: "Molecular pathological studies of Machado-Joseph disease"Brain Pathology. 7. 1273 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] S. Murayama et al.: "Molecular pothological study of Machedo-Joseph disease"Brain Pathology. 7. 1273 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Murayama S. et al.: "Regional and cellular expression of the dentatorubropallidoluysian atrophy."41. 599-605 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Murayama S.et al.: "Pathology of Machado-Joseph Disease" Society for Neuroscience Abstract. 25. (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] MURAYAMA S.et al :"Molecular pathological studies of Machado-Joseph disease." Brain Pathology. 7. 1273 (1997)

    • Related Report
      1997 Annual Research Report

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

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