Title of article :
HCV-core protein accelerates recovery from the insensitivity of liver cells to Fas-mediated apoptosis induced by an injection of anti-Fas antibody in mice
Author/Authors :
Arata Honda، نويسنده , , Masahiko Hatano، نويسنده , , Michinori Kohara، نويسنده , , Yutaka Arai، نويسنده , , Tety Hartatik، نويسنده , , Takashi Moriyama، نويسنده , , Michio Imawari، نويسنده , , Katsuro Koike، نويسنده , , Osamu Yokosuka، نويسنده , , Kunitada Shimotohno، نويسنده , , Takeshi Tokuhisa، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
8
From page :
440
To page :
447
Abstract :
Background/Aims: Hepatitis C virus (HCV) is a major etiologic agent of chronic hepatitis, cirrhosis, and hepatocellular carcinoma. The aim of this study was to elucidate pathological effects of HCV-core protein on liver cells. Methods: We have generated transgenic mice carrying HCV-core cDNA (Px-core) and pathologically examined livers of Px-core mice. Results: HCV-core protein was detectable in livers from lines 5 (C5) and 8 (C8) of Px-core transgenic mice. Since chronic hepatitis and cirrhosis precede hepatocellular carcinoma in patients with HCV infection, we tried to examine the effect of repetitive injection of a small dose of anti-Fas antibody in the transgenic mice. Surprisingly, an initial injection of anti-Fas antibody induced resistance of liver cells to the second injection of anti-Fas antibody in both Px-core and littermate control mice. The insensitivity of liver cells induced in the control mice continued for more than 24 weeks after the first injection but was broken within 1 week after partial hepatectomy. However, the sensitivity was restored in the Px-core mice within 12 weeks after the injection. Conclusion: HCV-core protein in liver cells may affect persistence of Fas-mediated liver cell injury.
Keywords :
hepatectomy , trans , Alanineantibody , HCV-coregenie mouse.aminotransaminase , Anti-Fasprotein
Journal title :
Journal of Hepatology
Serial Year :
2000
Journal title :
Journal of Hepatology
Record number :
585018
Link To Document :
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