Proliferative capability of hepatocytes and expression of G1-related cell cycle molecules in the development of liver cirrhosis in rats

  • Authors:
    • Fumi Funakoshi
    • Tsutomu Masaki
    • Yuko Kita
    • Misuzu Hitomi
    • Kazutaka Kurokohchi
    • Naohito Uchida
    • Seishiro Watanabe
    • Hitoshi Yoshiji
    • Shigeki Kuriyama
  • View Affiliations

  • Published online on: June 1, 2004     https://doi.org/10.3892/ijmm.13.6.779
  • Pages: 779-787
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Abstract

Liver cirrhosis is the end stage of various chronic liver diseases and its prognosis is very poor. One of the most important causes of liver cirrhosis appears to be impaired proliferative capability of hepatocytes caused by continuous hepatic damage. Cell cycle-related molecules have been shown to play essential roles in cell proliferation. Specifically, G1-related cell cycle molecules are important, because they are requisite for the entry into the cell cycle from the quiescent state. However, the role of these cell cycle molecules during the development of liver cirrhosis remains to be examined. In the present study, liver cirrhosis was produced in rats by intraperitoneally administering dimethylnitrosamine (DMN). Proliferative capability of hepatocytes estimated immunohistochemically by proliferating cell nuclear antigen staining was markedly increased at an early stage of cirrhosis development. However, it was gradually decreased thereafter and suppressed substantially at the time of cirrhosis manifestation. Cyclin D1 expression estimated by a real-time reverse transcription-polymerase chain reaction (RT-PCR) method was also increased markedly at an early stage of cirrhosis development but decreased substantially thereafter. mRNA levels of catalytic subunits of cyclin D1, cyclin-dependent kinase 4 (Cdk4) and Cdk6, did not show significant changes during the development of liver cirrhosis. Among G1-specific Cdk inhibitors, expression of p15INK4b and p16INK4a estimated by an RT-PCR method was increased according to the progression of cirrhosis and reached a peak at the time of cirrhosis manifestation. Conversely, p18INK4c expression did not change significantly during the development of liver cirrhosis. These results suggest that cyclin D1 plays an essential role in hepatocyte proliferation in response to hepatic damage. However, with the decrease of cyclin D1 expression and increase of p15INK4b and p16INK4a expression, proliferative capability of hepatocytes is severely impaired and extracellular matrix components are deposited to retrieve space lost by the destruction of hepatic parenchyma, resulting in establishment of liver cirrhosis.

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June 2004
Volume 13 Issue 6

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Spandidos Publications style
Funakoshi F, Masaki T, Kita Y, Hitomi M, Kurokohchi K, Uchida N, Watanabe S, Yoshiji H and Kuriyama S: Proliferative capability of hepatocytes and expression of G1-related cell cycle molecules in the development of liver cirrhosis in rats. Int J Mol Med 13: 779-787, 2004
APA
Funakoshi, F., Masaki, T., Kita, Y., Hitomi, M., Kurokohchi, K., Uchida, N. ... Kuriyama, S. (2004). Proliferative capability of hepatocytes and expression of G1-related cell cycle molecules in the development of liver cirrhosis in rats. International Journal of Molecular Medicine, 13, 779-787. https://doi.org/10.3892/ijmm.13.6.779
MLA
Funakoshi, F., Masaki, T., Kita, Y., Hitomi, M., Kurokohchi, K., Uchida, N., Watanabe, S., Yoshiji, H., Kuriyama, S."Proliferative capability of hepatocytes and expression of G1-related cell cycle molecules in the development of liver cirrhosis in rats". International Journal of Molecular Medicine 13.6 (2004): 779-787.
Chicago
Funakoshi, F., Masaki, T., Kita, Y., Hitomi, M., Kurokohchi, K., Uchida, N., Watanabe, S., Yoshiji, H., Kuriyama, S."Proliferative capability of hepatocytes and expression of G1-related cell cycle molecules in the development of liver cirrhosis in rats". International Journal of Molecular Medicine 13, no. 6 (2004): 779-787. https://doi.org/10.3892/ijmm.13.6.779