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Reconstruction of cirrhotic liver by means of extracellular matrix remodeling and differential stimulation of stem cells.

Research Project

Project/Area Number 14370394
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Digestive surgery
Research InstitutionHYOGO COLLEGE OF MEDICINE

Principal Investigator

IIMURO Yuji  Hyogo College of Medicine, Faculty of Medicine, Associate Professor, 医学部, 助教授 (30252018)

Co-Investigator(Kenkyū-buntansha) UEKI Takahiro  Hyogo College of Medicine, Faculty of Medicine, Research Associate, 医学部, 助手 (10309461)
IWASAKI Tsuyoshi  Hyogo College of Medicine, Faculty of Medicine, Associate Professor, 医学部, 助教授 (10151721)
FUJIMOTO Jiro  Hyogo College of Medicine, Faculty of Medicine, Professor, 医学部, 教授 (90199373)
HIRANO Tadamichi  Hyogo College of Medicine, Faculty of Medicine, Research Associate, 医学部, 助手 (90340968)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥14,000,000 (Direct Cost: ¥14,000,000)
Fiscal Year 2003: ¥6,400,000 (Direct Cost: ¥6,400,000)
Fiscal Year 2002: ¥7,600,000 (Direct Cost: ¥7,600,000)
KeywordsLiver cirrhosis / Gene therapy / Bone marrow transplant / Hepatocyte growth factor
Research Abstract

The purpose of the present study was to clarify the role of bone marrow-derived multipotent stem cells in the reconstructing process of cirrhotic livers during gene therapy with hepatocyte growth factor(HGF) cCDNA. [Methods]C57BL/6J mice received CCl_4(2.0ml/kg p.o.) for 6 weeks, developing liver cirrhosis. After irradiation of 900cGy, these animals underwent transplantation with bone marrow cells derived from LacZ transgenic mice. After the transplantation, some of the recipients were injected with HGF cDNA encapsulated in HVJ-liposome(200μg/body i.m.) once a week for 4 weeks. Control animal received empty HVJ-liposome. CCl_4 administration was continued once a week during this period. In these animals, recruitment of LacZ-positive bone marrow-derived cells into the liver was investigated immunohistochemically. Expression of c-Met/HGF receptor on the cell surface of bone marrow cells was also examined. [Results]Gene therapy with HGF cDNA effectively attenuated liver cirrhosis in the mice. During the reconstructing process of the cirrhotic livers, most of the donor derived LacZ-positive cells differentiated into the endothelial cells or sinusoidal endothelial cells. Small part of the LacZ-positive cells also differentiated into Kupffer cells, but not into hepatocyte, oval cells, or hepatic sttelate cells. Expression of c-Met was detected immunohistochemically on some of the bone marrow cells. [Conclusion]These results suggest that reconstruction of cirrhotic liver is efficiently carried out in combination of hepatic tissue-derived and bone-marrow-derived stem cell differentiation. HGF possibly accelerates differentiation of these stem cells into liver-constituting cells.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (17 results)

All Other

All Publications (17 results)

  • [Publications] Iimuro Y 他: "Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat."Gastroenterology. 124・2. 445-458 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nishio T, Iimuro Y 他: "Increased expression of collagenase in the liver induces hepatocyte proliferation with cytoplasmic accumulation of β-catenin in the rat."Journal of Hepatology. 38・4. 468-475 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Iimuro Y 他: "Strategy of gene therapy for liver cirrohosis and hepatocellular carcinoma."J Hepatobiliary Pancreat Surg.. 10・1. 45-47 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Ogushi I, Iimuro Y 他: "Nuclear factor kappa B decoy oligodeoxynucleotides prevent endotoxin-induced fatal liver failure in a murine model."Hepatology. 38・2. 335-344 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Harada N, Iimuro Y 他: "Inactivation of the small GTPase Rac1 protects the liver from ischemia/reperfusion injury in the rat."Surgery. 134・3. 480-491 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Iimuro Y, Nishio T, Morimoto T, Nitta T, Stefanovic B, Choi SK, Brenner DA, Yamaoka Y.: "Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat."Gastroenterology. 124(2). 445-458 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nishio T, Iimuro Y, Nitta T, Harada N, Yoshida M, Hirose T, Yamamoto N, Morimoto T, Brenner DA, Yamaoka Y.: "Increased expression of collagenase in the liver induces hepatocyte proliferation with cytoplasmic accumulation of beta-catenin in the rat."J Hepatol.. 38(4). 468-475 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Iimuro Y, Fujimoto J.: "Strategy of gene therapy for liver cirrohosis and hepatocellular carcinoma."J Hepatobiliary Pancreat Surg.. 10(1). 45-47 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Ogushi I, Iimuro Y, Seki E, Son G, Hirano T, Hada T, Tsutsui H, Nakanishi K, Morishita R, Kaneda Y, Fujimoto J.: "Nuclear factor kappa B decoy oligodeoxynucleotides prevent endotoxin-induced fatal liver failure in a murine model."Hepatology.. 38(2). 335-344 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Harada N, Iimuro Y, Nitta T, Yoshida M, Uchinami H, Nishio T, Hatano E, Yamamoto N, Yamamoto Y, Yamaoka Y.: "Inactivation of the small GTPase Rac1 protects the liver from ischemia/reperfusion injury in the rat."Surgery.. 134(3). 480-491 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Iimuro Y 他: "Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat."Gastroenterology. 124・2. 445-458 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Nishio T, Iimuro Y 他: "Increased expression of collagenase in the liver induces hepatocyte proliferation with cytoplasmic accumulation of β-catenin in the rat"Journal of Hepatology. 38・4. 468-475 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Iimuro Y 他: "Strategy of gene therapy for liver cirrohosis and hepatocellular carcinoma."J Hepatobiliary Pancreat Surg.. 10・1. 45-47 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Ogushi I, Iimuro Y 他: "Nuclear factor kappa B decoy oligodeoxynucleotides prevent endotoxin-induced fatal liver failure in a murine model."Hepatology. 38・2. 335-344 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Harada N, Iimuro Y 他: "Inactivation of the small GTPase Rac1 protects the liver from ischemia/reperfusion injury in the rat."Surgery. 134・3. 480-491 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Iimuro Y 他: "Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat"Gastroenterology. 124・3. 445-458 (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] Nishio T, Iimuro Y 他: "Increased expression of collagenase in the liver induces hepatocyte proliferation with cytoplasmic accumulation of β-catenin in the rat"Journal of Hepatology. (In press ). (2003)

    • Related Report
      2002 Annual Research Report

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Published: 2002-04-01   Modified: 2016-04-21  

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