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Establishment of cryo-preservation method for ovary and testis and storage of wild mouse genes.

Research Project

Project/Area Number 08680918
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Laboratory animal science
Research InstitutionTHE TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE

Principal Investigator

TAYA Choji  THE TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE,DEPARTMENT OF LABORATORY ANIMAL SCIENCE,RESEARCH STAFF, 実験動物研究部門, 研究員 (90175456)

Project Period (FY) 1996 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1997: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
KeywordsCryo-preservation of ovary / Cryo-preservation of testis / Wild mouse genes / Preservation of gene resources
Research Abstract

This study aimed at an establishment of storage system for wild mouse genome by freezing of ovary and testis from a viewpoint of preservation of gene resources.
1. Establishment of cryo-preservation method for ovary and strage of wild mouse genes.
Successful freezing conditions of ovaries were detected in a series of experiments using laboratory mice. When the freesing method was applied to ovaries of MSM inbred strain derived from Japanese wild mice, mice derived from frozen ovaries were obtained, though litter sizes were very small.
2. Establishment of cryo-preservation method for testis
freezing injuries of newborn mouse testes were examined histologically at various points of a freezing course. A lot of germ cells retained a normal morphology in the program of slow cooling til -40゚C before immersion into LN2.
In order to confirm the growth of germ cells and the production of spermatozoa, the frozen newborn testis were transplanted into histocompatible adult testis. In the case of a freezing program described above, at 14 days after transplantation meiotic germ cells were observed and at six weeks spermatozoa were detected in the seminiferous tubules derived from the frozen testes, though it has not been confirmed whether they have a capacity of fertilization to oocytes.
A reconstitution of thawed testis to a host reproductive system is under investigation.

Report

(3 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Shimmoto, M.: "Generation and charactrzaton of transgenic mice expressing a human mutant d-galactosidase with af R301Q substitution causing a variant form of Fabry disease." FEBS Lett.417. 89-91 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ishii, S: "α-Galactosidase transgenic mouse:Heterogenous gene expression and posttranslational glycosylation." Glycoconjugate J.(in press). (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Shimmoto, M.et al.: "Generation and characterization of transgenic mice expressing a human mutant alpha-galactosidase with an R301Q substitution causing a variant form of Fabry disease" FEBS Lett.417. 89-91 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ishii, S.et al.: "Alpha-garactosidase transgenic mouse : Heterogenous gene expression and posttranslational glycosylation." Glycoconjugate J.(in press). (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Shimmoto,M.: "Generation and characterization of transgenic mice expressing a human mutant α-galactosidase with an R301Q substitution causing a variant form of Fabry disease." FEBS Lett.417. 89-91 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Ishii S.: "α-Galactosidase transgenic mouse:Heterogenous gene expression and posttranslational glycosylation." Glycoconjugate J.(in press). (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1996-04-01   Modified: 2016-04-21  

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