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Investigation on gene therapy for congenital bleeding tendency

Research Project

Project/Area Number 03454523
Research Category

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

Allocation TypeSingle-year Grants
Research Field Hematology
Research InstitutionNagoya University

Principal Investigator

SAITO Hidehiko  Nagoya University School of Medicine, Professor, 医学部, 教授 (20153819)

Co-Investigator(Kenkyū-buntansha) EMI Nobuhiko  Nagoya University School of Medicine, Senior Resident, 医学部, 医員
TANIMOTO Mitsune  Nagoya University School of Medicine, Assistant Professor, 医学部, 助手 (10240805)
TAKAMATSU Junki  Nagoya University School of Medicine, Associate Professor, 医学部, 助教授 (80221365)
Project Period (FY) 1991 – 1992
Project Status Completed (Fiscal Year 1992)
Budget Amount *help
¥5,600,000 (Direct Cost: ¥5,600,000)
Fiscal Year 1992: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1991: ¥4,300,000 (Direct Cost: ¥4,300,000)
Keywordsfactor IX / expression vector / retroviral vector / pL9RNL / gene therapy / VII因子 / レトロウイルスベクター / 第IX因子 / レトロウイルスベクタ-
Research Abstract

We constructed a new factor IX expression vector containing a full length factor IX cDNA.The Moloney Murine Leukemia Virus (MoMLV)-based retroviral vector pLRNL was cloned with the entire coding region of human factor IX down stream of the promoter of Rous sarcoma virus, givinh rise to the construct pL9RNL.The GP+E 86 packaging cell was transfected with pL9RNL and two mouse fibroblast cell lines (PA317 and NIH3T3) were infected with the virus generated from PA317 cell. During the 24 hr culture period, the maximum 1.2mug of factor IX was secreted into the medium from 10^6 of GP+E 86 cells. Factor IX in the culture media had the relatively normal procoagulant activity and was barium-citrate precipitated. Western blotting analysis of the barium-citrate precipitated revealed that a single chain 50Kd protein indistinguishable from the plasma-derived factor IX was produced in these three cells. The retroviral expression system that we utilized herein may contribute to the study of recombinant wild type or various mutant factor IX,and to the basic study for the future gene therapy.

Report

(3 results)
  • 1992 Annual Research Report   Final Research Report Summary
  • 1991 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Saito,H.et al.: "Construction and its expression of a new retroviral vector Containing on human Coagulation factor IX CDNA" Thromb.Res.69. 387-393 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Saito, H.et al: "Construction and its expression of a new retroviral vector containing a human blood coagulation factor IX cDNA." Thromb Res. 69. 387-393 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Matsushita, T.: "Construction and its expression of a new retroviral vector containing a human blood coagulation factor XI cDNA." Thromb Res in press.

    • Related Report
      1992 Annual Research Report
  • [Publications] Yamamoto, K.: "Impaired secretion of the elongated mutant of protein C(protein C-Nagoya): Molecular and cellular basis for hereditary protein C deficiency." J Clin Invest. 90. 2439-2446 (1992)

    • Related Report
      1992 Annual Research Report
  • [Publications] Yamamoto, K.: "Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C." J Lab Clin Med. 119. 682-689 (1992)

    • Related Report
      1992 Annual Research Report
  • [Publications] Yamamoto, K.: "Two novel sequence polymorphisms of the human protein C gene." Nuc Acid Res. 19. 6973- (1991)

    • Related Report
      1992 Annual Research Report
  • [Publications] Yamamoto, K.: "Genotype establishments for protein C deficiency by use of a DNA polymorphism in the gene." Blood. 77. 2633-2636 (1991)

    • Related Report
      1992 Annual Research Report
  • [Publications] Ichinose, A.: "Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis." Proc Natl Acad Sci USA. 88. 115-119 (1991)

    • Related Report
      1992 Annual Research Report
  • [Publications] Hamaguchi,M.: "Three distinct point mutations in the factor IX gene of three Japanese CRM^+ Hemophilia B patients (Factor IX B_M Nagoya 2,Factor IX Nagoya 3 and 4.)" Thromb Haemost. 65. 514-520 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] Matsushita,T.: "Direct carrier detection in hemophilia B Kindreds:use of modified primers (mutagenic primers) for enzymatic amplification of the factor IX gene." Thromb Res. 63. 355-361 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] Sugiura,I.: "Three distinct point mutations of the von Willebrand factor genen in four patients with type IIA von Willebrand disease." Thromb Haemost.

    • Related Report
      1991 Annual Research Report
  • [Publications] Saito,H.: "Recent Advances in Thrombosis and Fibrinolysis" Academic Press,Inc., 363 (1991)

    • Related Report
      1991 Annual Research Report

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Published: 1991-04-01   Modified: 2016-04-21  

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