Hepatic failure and liver cell damage in acute Wilson's disease involve CD95 (APO-1/Fas) mediated apoptosis

被引:209
作者
Strand, S
Hofmann, WJ
Grambihler, A
Hug, H
Volkmann, M
Otto, G
Wesch, H
Mariani, SM
Hack, V
Stremmel, W
Krammer, PH
Galle, PR
机构
[1] Univ Heidelberg Hosp, Dept Gastroenterol, D-69115 Heidelberg, Germany
[2] Inst Pathol, D-69120 Heidelberg, Germany
[3] ZMBH, Ctr Mol Biol, D-69120 Heidelberg, Germany
[4] Dept Surg, D-69120 Heidelberg, Germany
[5] German Canc Res Ctr, Tumorimmunol Program, D-69120 Heidelberg, Germany
[6] German Canc Res Ctr, Radiol Program, D-69120 Heidelberg, Germany
[7] German Canc Res Ctr, Div Immunochem, D-69120 Heidelberg, Germany
关键词
D O I
10.1038/nm0598-588
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Wilson's disease can result in fulminant liver failure due to hepatic copper overload. The CD95 system mediates apoptosis and has been demonstrated to be involved in liver disease. In this study CD95 mediated apoptosis was investigated in patients with fulminant hepatic failure in the course of Wilson's disease and in an in vitro model of copper treated human hepatoma cells. In patients, hepatic expression of CD95 and CD95L mRNA and apoptosis were detected. Copper overload in vitro resulted in hepatocytic apoptosis which could be reduced with a neutralizing anti-CD95L antibody. Copper treatment of hepatocytes results in activation of the CD95 system and induction of apoptosis which is operative during the course of hepatic failure in acute Wilson's disease.
引用
收藏
页码:588 / 593
页数:6
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