• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2000 Fiscal Year Final Research Report Summary

Molecular investigation on the fulminant hepatitis-resistant model animals

Research Project

Project/Area Number 10470253
Research Category

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

Allocation TypeSingle-year Grants
Section一般
Research Field Digestive surgery
Research InstitutionHAMAMATSU UNIVERSITY SCHOOL OF MEDICINE (1999-2000)
Akita University (1998)

Principal Investigator

MIURA Naoyuki  Hamamatsu University, School of Medicine, Professor, 医学部, 教授 (40165965)

Co-Investigator(Kenkyū-buntansha) SATO Eiji  Hamamatsu University, School of Medicine, Res. Associate, 医学部, 助手 (70118751)
WU Yi-xin  Hamamatsu University, School of Medicine, Res. Associate, 医学部, 助手 (60283363)
YOSHIDA Nobuaki  University of Tokyo, Inst. Medical Science, Professor, 医科学研究所, 教授 (10250341)
Project Period (FY) 1998 – 2000
KeywordsRb protein / Transgenic mice / Apoptosis / Fulminant hepatitis / Fas antigen / TNFα / Hepatocellular carcinoma / Nodule
Research Abstract

Two lines of the transgenic mice in which the human Rb cDNA was controlled under the) kbp of rat hepatocyte nuclear factor-1 (HNF-1) promoter/enhancer were generated. Transgenic mice, line A (TGA) had about 11 copies of the transgenes per haploid and line B (TGB) had about 4 copies of the transgenes. By Western blot analysis, we observed that a large amount of Rb protein was expressed in the liver of TGA mice and a small amount of Rb protein was expressed in that of TGB mice. In control mice, injection of anti-Fas antibody and TNFα induced increase of GOT and GPT in serum, hemorrhages and hepatocyte apoptosis in the histology. However, in TGA mice, the increase in GOT and GPT was marginal and no hemorrhages and apoptosis were detected In TGB mice, the increase in GOT and GPT was moderate and apoptosis of the substantial number of hepatocytes was observed, but no hemorrhages. In order to investigate the molecular mechanism of anti-apoptotic condition, we did the western blot analysis of … More apoptosis-related proteins. Fas, Bcl-2, Bcl-X, Bid, Bad, ICE, CPP32, E2F1, E2F2, E2F3, E2F4, E2F5 and p53 proteins had no differences between control mice and Rb transgenic mice. However, the Bax protein was decreased in Rb transgenic mice compared to control mice. This suggests that the Bax protein is on e of the contributing proteins for the anti-apoptotic condition.
Next we investigated whether the Rb transgenic mice showed resistance to chemical carcinogenesis. We inject diethylnitrosamine into the peritoneal cavity at the age of 6 weeks and treated phenobarbital in drinking water for 35 weeks. After the experiment, the mice were sacrificed to make histological sections for counting the numbers of hepatocellular carcinoma and hepatic nodule. In control mice, a large number of nodules and several hepatocellular carcinoma were developed. In contrast, the number of nodules was greatly reduced and no hepatocellular carcinomas were detected in Rb transgenic mice. These results indicate that the Rb protein act as an anti apoptotic agent and an anti-tumorigenic agent in the liver in vivo. Less

  • Research Products

    (16 results)

All Other

All Publications (16 results)

  • [Publications] Terada,K.: "Restoration of holoceruloplasmin synthesis in LEC rat after infusion of recombinant adenovirus bearing WND cDNA."J.Biol.Chem.. 273. 1815-1820 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Komatsu,M.: "Copper-transporting P-type adenosine triphosphatase (ATP7B) is associated with cisplatin resistance."Cancer Res.. 60. 1312-1316 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Harada,M.: "Role of ATP7B in biliary copper excretion in a human hepatoma cell line and normal rat hepatocytes."Gastroenterology. 118. 921-928 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Eguchi,A.: "Identification and characterization of cell lines with a defect in a post-adsorption stage of Sendai virus-mediated membrane fusion."J.Biol.Chem.. 275. 17549-17555 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Roelofsen,H.: "Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion."Gastroenterology. 119. 782-793 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ichihara,T.: "Resistance to fulminant hepatitis and carcinogenesis conferred by overexpression of retinoblastoma protein in mouse liver."Hepatology. (印刷中).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Sugiyama,T.: "Tissue Engineering for Therapeutic Use 3"Elsevier Science B.V.. 161 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Miura,N.: "Etiology and morphogenesis of congenital heart disease : Twenty years of progress in genetics and developmental biology"Futura Publishing Co.. 389 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Terada, K.et al.: "Restoration of holoceruloplasmin synthesis in LEC rat after infusion of recombinant adenovirus bearing WND cDNA."J.Biol. Chem.. 273. 1815-1820 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Komatsu, M.et al.: "Copper-transporting P-type adenosine triphosphatase (ATP7B) is associated with cisplatin resistance."Cancer Res.. 60. 1312-1316 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Harada, M.et al.: "Role of ATP7B in biliary copper excretion in a human hepatoma cell line and normal rat hepatocytes."Gastroenterology. 118. 921-928 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Eguchi, A.et al.: "Identification and characterization of cell lines with a defect in a post-adsorption stage of Sendai virus-mediated membrane fusion."J.Biol. Chem.. 275. 17549-17555 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Roelofsen, H.et al.: "Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion."Gastroenterology. 119. 782-793 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ichihara, T.et al.: "Resistance to fulminant hepatitis and carcinogenesis conferred by overexpression of retinoblastoma protein in mouse liver."Hepatology. (in press.).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Sugiyama, T.et al.: "Tissue Engineering for Therapeutic Use 3"Elsevier Science B.V.. (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Miura, N.et al.: "Etiology and morphogenesis of congenital heart disease : Twenty years of progress in genetics and developmental biology"Futura Publishing Co.. (2000)

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

URL: 

Published: 2002-03-26  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi