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A Role of Protein Tyrosine Phosphorylation in Bile Ductular Metaplasia of Hepatocytes

Research Project

Project/Area Number 11670203
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionAkita University

Principal Investigator

NISHIKAWA Yuji  Akita University School of Medicine, Associate Professor, 医学部, 助教授 (90208166)

Co-Investigator(Kenkyū-buntansha) ENOMOTO Katsuhiko  Akita University School of Medicine, Professor, 医学部, 教授 (20151988)
YOSHIOKA Toshiaki  Akita University School of Medicine, Research Associate, 医学部, 助手 (80302264)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥2,100,000 (Direct Cost: ¥2,100,000)
KeywordsBile ductular reaction (metaplasia) / Hepatocytes / Bile duct cells / Liver fibrosis / Chronic liver disease / Three-dimensional culture / Liver non-parenchymal cells / Kupffer cells / 蛋白質チロシンリン酸化 / バナジウム酸 / 肝硬変 / 培養
Research Abstract

Bile ductules are known to increase in the portal area in chronic liver diseases with portal fibrosis and inflammation (ductular reaction). It has been considered that newly formed bile ductules may be derived from periportal hepatocytes, although the mechanism is not clear. In this study, we investigated a possible role of protein tyrosine phosphorylation in the bile ductular metaplasia of hepatocytes using a three dimensional culture system. We also studied whether liver non-parenchymal cells, especially Kupffer cells, affected hepatocyte differentiation. Summary of our results are as follows.
(1) When sheroidal aggregates of mature rat hepatocytes were embedded within a three-dimensional collagen gel matrix, dendritic cellular processes elongated from the aggregates and these processes expressed bile duct-specific cytokeratins, such as cytokeratins 19 and 20. These cellular processes formed bile duct-like tubular structures with distinct basal membrane after 3 weeks in vitro.
(2) A prototype protein tyrosine phosphatase inhibitor, sodium orthovanadate, which increased protein tyrosine phosphorylation levels of cellular proteins, promoted the dendritic morphogenesis and expression of the bile duct-specific cytokeratins of cultured hepatocytes.
(3) The dendritic morphogenesis of cultured hepatocytes was markedly enhanced by soluble factors derived from liver non-parenchymal cells, especially interleukin 6 and transforming growth factor α, which are known to be secreted by Kupffer cells.
Our data suggested that bile ductular differentiation of mature hepatocytes within the collagenous matrix might be regulated by protein tyrosine phosphorylation and affected by non-parenchymal cell-derived soluble factors.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Yuji Nishikawa, et al.: "Inhibition of hepatoma cell growth in vitro by arylating and non-arylating K vitamin analogs"The Journal of Biological Chemistry. 274. 34803-34810 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Osamu Muto, et al.: "HGF/SF-induced spreading of MDCK cells correlates with disappearance of barmotin/7H6, a tight junction-associated protein, from the cell membrane"Cell Biology International. 24. 439-446 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Y,Nishikwa, et al.: "Inhibition of hepatoma cell growth in vitro by arylating and non-arylating K vitamin analogs"The Journal of Biological Chemistry. 274. 34803-34810 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] O.Muto, et al.: "HGF/SF-induced spreading of MDCK cells correlates with disappearance of barmotin/7H6, a tight junction-associated protein, from the cell membrane"Cell Biology International. 24. 439-446 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yuji Nishikawa, et al.: "Inhibition of hepatoma cell growth in vitro by arylating and non-arylating K vitamin analogs"The Journal of Biological Chemistry. 274(49). 34803-34810 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Osamu Muto, et al.: "HGF/SF-induced spreading of MDCK cells correlates with disappearance of barmotin/7H6, a tight junction-associated protein, from the cell membrane"Cell Biology International. 24(7). 439-446 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yuji Nishikawa: "Inhibition of Hepatoma Cell Growth in Vitro by Arylating and Non-arylating K Vitamin Analogs SIGNIFICANCE OF PROTEIN TYROSINE PHOSPHATASE INHIBITION"The Journal of Biological Chemistry. 274(49). 34803-34810 (1999)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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