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Gene therapy for neurogical abnormality using mouse model of lipidosis

Research Project

Project/Area Number 13670841
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionThe Jikei University School of Medicine

Principal Investigator

IDA H (2002)  Jikei Univ, Dept. of Pediatrics asso prof, 医学部, 助教授 (90167255)

洲鎌 盛一 (2001)  東京慈恵会医科大学, 医学部, 助手 (10154452)

Co-Investigator(Kenkyū-buntansha) SUGAMA S  Jikei Univ, Dept. of Pediatrics assi prof, 医学部, 講師 (10154452)
OHASHI T  Jikei Univ, Dept. of Pediatrics asso prof, 医学部, 助教授 (60160595)
長谷川 頼康  東京慈恵会医科大学, 医学部, 助手 (60256435)
井田 博幸  東京慈恵会医科大学, 医学部, 講師 (90167255)
Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 2002: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2001: ¥1,600,000 (Direct Cost: ¥1,600,000)
Keywordslipidosis / gene therapy / mouse model / CNS involvement / 神経細胞 / Krabbe病 / Twitcherマウス / アデノウイルスベクター / 胎児治療
Research Abstract

We investigated the effectiveness of gene therapy to lipidosis mouse model. Krabbe disease is caused by a deficiency of galactocerebiostdase (GALC). This enzyme defect resuts in accumulation of psychosine which leads severe demyelination and the occurrence of globoid cells.Twitcher mouse is a murine model of human Krabbe disease. This model mouse manifests twitching and body weight loss, and ultimately dies at 5 weeks after birth. We injected recombinant adenovirus encoding GALC into the lateral ventricle of twitcher mice at birth. Significant improvements in motor functions, body weight and twitching and a prolonged life span were observed. GALC activity was increased to 15% that of normal littermates and psychosine concentration was decreased to 55% that of untreated twitcher mice at postnatal day 15 (PND 15). The number of globoid cells in brain stem was also reduced significantly at PND 35. In contrast, when adenoviruses were injected to the twitcher mice at PND 15, almost no improvements were observed. These data demonstrate that the timing of gene transfer may be of great importance in Krabbe disease.

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (20 results)

All Other

All Publications (20 results)

  • [Publications] Ida H, et al.: "Effects of enzyme replacement therapy in 13 Japanese pediatric patients with Gaucher disease"Eur J Pediatr. 160. 21-25 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Shen J.S, Ida H, et al.: "Establishement and characterization of spontaneously immortalized Schwann cells from murine globoid cell leukodystrophy(Twitcher)"J Neuroscience Res. 68. 588-594 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Mikami T, Ida H, et al.: "Signaling pathway for radiation-induced apoptosis in the lymphoblasts from neuronopathic (type A) and non-neuronopathic (type B) forms of Niemann-Pick disease"J Neuro Sci. 199. 39-43 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Komatu M, Ida H, et al.: "Evidence for the association of ultraviolet-C and H2O2-induced apoptosis with acid sphingomyelinase activation"Biochim Biophys Acta. 1533. 47-54 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Lee Y.S, Ida H, et al.: "Gaucher disease : Compound heterozygote with RecNciI and L444P mutations"J Tropical Pediatr. 47. 115-117 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Tsuda M, Ida H, et al.: "A newly recognized missennse mutation in the GLUT2 gene in a patient with Fanconi-Blckel syndrome"Eur J Pediatr. 160. 867 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Ida.H, Rennert OM, Kobayashi M and Eto Y: "Effects of enzyme replacement therapy in 13 Japanese pediatric patients with Gaucher disease."Eur J Pediatr. 160. 21-5 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Shen J.S, Watabe.K, Meng X.L, Ida H, Ohashi Tand Eto Y: "Establishement and characterization of spontaneously immortalized Schwann cells from murine globoid cell leukodystrophy (Twitcher)."J Neuroscience Res.. 68. 588-594 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Mikami.T, Takahasi.T, Ishida.A, Minamiya.Y, Ida.H, Takada.G.: "Signaling pathway for radiation-induced apoptosis in the lymphoblasts from neuronopathic (type A) and-non-neuronopathtic (type B) forms of Niemann-Pick disease."J Neuro Sci.. 199. 39-43 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Komatu.M, Takahasi.T, Abe.T, Takahasi.I, Ida.H, Takada.G.: "Evidence for the association of ultraviolet-C and H2O2-induced apoptosis with acid sphingomyelinase activation."Biochim Biophys Acta. 1533. 47-54 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Tsuda.M, Kitasawa.E, Ida.H, Eto.Y, Owada.M.: "A newly recognized missennse mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome."Eur J Pediatr. 160. 867 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Lee Y.S, PohL.K.S, Ida.H, Loke K.Y.: "Type II Gaucher disease:Compound heterozygote with RecNcil and L444P mutation."J Tropical Pediatr. 47. 115-117 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Shen J.S, Ida H, et al.: "Establishement and characterization of spontaneously immortalized Schwann cells from murine globoid cell leukodystrophy (Twitcher)"J Neuroscience Res. 68. 588-594 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Mikami T, Ida H, et al.: "Signaling pathway for radiation-induced apoptosis in the lymphoblasts from neuronopathic (type A) and non-neuronopathic (type B) forms of Niemann-Pick disease"J Neuro Sci. 199. 39-43 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Sugama S., Kimura A., et al.: "Frontal lobe dementia with abnormal cholesterol metabolism and heterozygous mutation in sterol 27-hydroxylase gene"J Inherit Metab Dis. 24. 379-92 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Sugama S., Soeda A.: "Magnetic resonance imaging in three children with kernicterus"Pediatr Neurol. 25. 328-31 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Sugama S., Eto Y.: "Behavioral and cognitive profiles in a patient with selective caudate lesions due to neonatal brain insults"Jikeikai Med J. 48. 123-30 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Sugama S., Eto Y.: "Cognitive profile in a patient with Dandy-Walker Malformation and normal intelligence"Jikeikai Med J. 48. 131-7 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Sugama S., Eto Y.: "Clinical profile of patients with basal ganglia and thalamic lesions due to hypoxic-ischemic brainn damaqe"Jikeikai Med J. 48. 7-13 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Sugama S., Eto Y.: "Role of the cerebellum in cognition in a case of cerebellar hypoplasia and occipital cephalocele"Jikeikai Med J. 47. 261-8 (2000)

    • Related Report
      2001 Annual Research Report

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Published: 2001-04-01   Modified: 2016-04-21  

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