| Literature DB >> 12479930 |
Kazuo Yoneyama1, Takashi Goto, Kouichi Miura, Ken ichirou Mikami, Shigetoshi Ohshima, Kunio Nakane, Jiun Guey Lin, Masashiro Sugawara, Norio Nakamura, Kamon Shirakawa, Masafumi Komatsu, Sumio Watanabe.
Abstract
In viral hepatitis, binding of Fas ligand (FasL) with Fas expressed on the surfaces of infected hepatocytes induces apoptosis, removing hepatitis virus along with infected hepatocytes. We measured serum concentrations of soluble Fas (sFas) and FasL (sFasL), expression of membrane-bound FasL, and expression of FasL-mRNA in patients with chronic hepatitis C without cirrhosis (CH-C) and chronic hepatitis C with liver cirrhosis (LC-C). In CH-C, sFasL concentrations were lower and FasL-mRNA expression was significantly less than in volunteers. In LC-C, sFas concentrations were significantly greater than in healthy volunteers, while sFasL, membrane-bound FasL expression, and FasL-mRNA expression did not show significant differences. We also examined these variables over 24 h following the first interferon (IFN) treatment in patients with CH-C. Serum concentrations of sFas and sFasL, and FasL-mRNA expression increased markedly beyond amounts present before IFN injection until 12 h after IFN injection. However, membrane-bound FasL expression decreased until 6 h, followed by an increase until 24 h. Our findings suggest that the ratio of membrane-bound FasL to sFasL may be regulated to remove virally infected cells in CH-C. In addition, apoptosis mediated by the Fas/FasL system may be influenced by IFN injection for treatment of CH-C.Entities:
Year: 2002 PMID: 12479930 DOI: 10.1016/s1386-6346(02)00137-7
Source DB: PubMed Journal: Hepatol Res ISSN: 1386-6346 Impact factor: 4.288