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1995 Fiscal Year Final Research Report Summary

Three-dimensional imaging of cells and tissues for the clarification of pathogenesis of inherited metabolic diseases.

Research Project

Project/Area Number 06670847
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Pediatrics
Research InstitutionThe Tokyo Metropolitan Institute of Medical Science

Principal Investigator

SAKURABA Hitoshi  The Tokyo Metropolitan Institute of Medical Science, Department of Clinical Genetics, Research Scientist, 臨床遺伝学研究部門, 研究員 (60114493)

Co-Investigator(Kenkyū-buntansha) FUJISHIRO Issei  Ochanomizu University, Department of Information Sciences, Faculty of Science, A, 理学情報科学科, 助教授 (00181347)
KOTANI Masaharu  The Tokyo Metropolitan Institute of Medical Science, Department of Tumor Immunol, 臨床遺伝学研究部門, 研究員 (10195737)
ITOH Kohji  The Tokyo Metropolitan Institute of Medical Science, Department of Clinical Gene, 臨床遺伝学研究部門, 研究員 (00184656)
Project Period (FY) 1994 – 1995
KeywordsLipidosis / Metachromatic leukodystrophy / Fabry disease / Volume visualization / Three-dimensional images / confocal laser scanning microscopy
Research Abstract

The basic understanding of sphingolipidosis requires study of the clinical, biochemical, and pathological aspects. To study the pathological aspects, the organs and tissues affected by the disease must be observed. We have used volume visualization techniques to create three-dimensional (3D) images of a brain affected by late infantile metachromatic leukodystrophy (MLD) and of a biopsied kidney tissue affected by Fabry disease.
The 3D brain images of a MLD patient showed clearly, stereographically, and non-invasively the intracerebral lesion. This lesion, which indicated hyperintensity in magnetic resonance (MR) images, extended throughout the periventricular white matter. The 3D brain images provided to integrate information in combination with two-dimensional MR images. Volumetric ray-casting was useful in obtaining directly images of the entire brain and in allowing an intuitive understanding of the extension of the lesion in three dimensions and of the extent of the defects in the MLD brain. Isosurfacing facilitated a clear extraction of the lesion located by volumetric ray-casting. Each technique used in this study playd a role in visualization and their use was complementary.
The combination of a laser scanning confocal microscopic analysis and the volume visualization showed stereographically the accumulation of globotriaosylceramide in the biopsied kidney tissue from a patient with Fabry disease.
3D images will promote basic and clinical investigations of sphingolipidosis.

  • Research Products

    (38 results)

All Other

All Publications (38 results)

  • [Publications] Ishii, S.: "Human α-galactosidase gene expression: significance of two peptide regions encoded by exons 1-2 and 6." Biochim. Biophys. Acta. 1204. 265-270 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsuji, A.: "Lysosomal enzyme replacement using α_2-macroglobulin as a transport vehicle." J. Biochem.115. 937-944 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kotani, M.: "Evidence for direct binding to intracellularly distributed ganglioside G_<M2> to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblasts." Cell Structure and Function. 19. 81-87 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Oshima, A.: "Intracellular processing and maturation of mutant gene products in hereditary β-galactosidase deficiency(β-galactosidosis)." Hum. Genet.93. 109-114 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii, N.: "Normal serum β-galactosidase in juvenile GM1 gangliosidosis." Pediatr. Neurol.10. 317-319 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Satake, A.: "Distribution of lysosomal protective protein in human tissues." Biochem. Biophys. Res. Commun.205. 38-43 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Itoh, K.: "Protective protein as an endogenous endothelin degradation enzyme in human tissues." J. Biol. Chem.270. 515-518 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Okumiya, Y.: "α-Galactosidase gene mutations in Fabry disease: heterogeneous expressions of mutant enzyme proteins." Hum. Genet.95. 557-561 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii, S.: "The functional role of glutamine-280 and threonine-282 in human α-galactosidase." Biochim. Biophys. Acta. 1270. 163-167 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii, N.: "Clinical and molecular analysis of a Japanese boy with Morquio B disease." Clin. Genet.48. 103-108 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nakao, S.: "An atypical variant of Fabry's disease in men with left ventricular hypertrophy." N. Engl. J. Med.333. 288-293 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kuroki, Y.: "A nobel missense mutation(C552Y) is present in the β-hexosaminidase β-subunit gene of a Japanese patient with infantile Sandhoff disease." Biochem. Biophys. Res. Commun.212. 564-571 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii, N.: "β-Galactosidosis(genetic β-galactosidase deficiency): clinical and genetic heterogeneity of the skeletal form." Develop. Brain Dysfunct.8. 40-50 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Okumiya, T.: "Galactose stabilizes various missense mutants of α-galactosidase in Fabry disease." Biochem. Biophys. Res. Commun.214. 1219-1224 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Itoh, K.: "Immunofluorescence analysis of globotriaosylceramide accumulated in the hearts of variant hemizygotes and heterzygotes with Fabry disease." Am. J. Cardiol.(in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takenaka, T.: "Coexistence of gene mutations causing Fabry Disease and Duchenne muscular dystrophy in a Japanese boy." Clin. Genet.(in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii, S.: "Aggregation of the inactive-form of human α-galactosidase in the endoplasmic reticulum." Biochem, Biophys. Res. Commun.(in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shimmoto, M.: "A human protective protein gene partially overlaps the gene encoding phospholipid transfer protein on the complementary strand of DNA." Biochem, Biophys. Res. Commun.(in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Suzuki, Y.: "The metabolic and molecular bases of inherited disease." McGraw-Hill(New York), 38 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishii S., et al.: "Human alpha-galactosidase gene expression : significance of two peptide regions encoded by exons 1-2 and 6." Biochim.Biophys.Acta.1204. 265-270 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tsuji A., et al.: "Lysosomal enzyme replacement using alpha_2-macroglobulin as a transport vehicle." J.Biochem.115. 937-944 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kotani, M., et al.: "Evidence for direct binding of intracellularly distributed ganglioside G_<M2> to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblasts." Cell Structure and Function. 19. 81-87 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Oshima, A,, et al: "Intracellular processing and maturation of mutant gene products in hereditary beta-galactosidase deficiency (beta-galactosidosis)" Hum.Genet.93. 109-114 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishii, N., et al.: "Normal serum beta-galactosidase in juvenile GM1 gangliosidosis." Pediatr.Neurol.10. 317-319 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Satake, A., et al: "Distribution of lysosomal protective protein in human tissues." Biochem.Biophys.Res.Commun.205. 38-43 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Itoh, K., et al.: "Protective protein as an endogenous endothelin degradation enzyme in human tissues." J.Biol. Chem.270. 515-518 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Okumiya, Y., et al.: "alpha-Galactosidase gene mutations in Fabry disease : heterogeneous expressions of mutant enzyme proteins." Hum.Genet.95. 557-561 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishii, S., et al.: "The functional role of glutamine-280 and threonine-282 in human alpha-galactosidase." Biochim.Biophys.Acta.1270. 163-167 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishii, N., et al.: "Clinical and molecular analysis of a Japanese boy with Morquio B disease." Clin.Genet.48. 103-108 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nakao, S., et al.: "An atypical variant of Fabry's disease in men with left ventricular hypertrophy." N.Engl.J.Med.333. 288-293 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuroki, Y., et al.: "A nobel missense mutation (C552Y) is present in the beta-hexosaminidase beta-subunit gene of a Japanese patient with infantile Sandhoff disease" Biochem.Biophys.Res.Commun.212. 564-571 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishii, N., et al.: "beta-Galactosidosis (genetic beta-galactosidase deficiency) : clinical and genetic heterogeneity of the skeletal form." Develop.Brain Dysfunct.8. 40-50 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Okumiya, T., et al.: "Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease." Biochem.Biophys.Res.Commum. 214. 1219-1224 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Itoh, K., et al.: "Immunofluorescence analysis of globotriaosylceramide accumulated in the hearts of variant hemizygotes and heterzygotes with Fabry disease." Am.J.Cardiol. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takenaka, T., et al.: "Coexistence of gene mutations causing Fabry Disease and Duchenne muscular dystrophy in a Japanese boy." Clin.Genet.(in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishii, S., et al.: "Aggregation of the inactive-form of human alpha-galactosidase in the endoplasmic reticulum." Biochem.Biophys. Res.Commun.(in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shimmoto, M., et al.: "A human protective protein gene partially overlaps the gene encoding phospholipid transfer protein on the complementary strand of DNA." Biochem.Biophys.Res.Commun.(in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Suzuki, Y., et al.: beta-Galactosidase deficiency (beta-Galactosidosis) : GM1 gangliosidosis and Morquio B disease. The metabolic and molecular bases of inherited disease. 7ht ed. (Scriver, C.R., Beaudet, A.L., Sly, W.S., Valle, D., eds.). McGraw-Hill (New York), 2785-2823 (1995)

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

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Published: 1997-03-04  

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