Dissection of the multiple mechanisms of TNF‐α‐induced apoptosis in liver injury

WX Ding, XM Yin - Journal of cellular and molecular medicine, 2004 - Wiley Online Library
Journal of cellular and molecular medicine, 2004Wiley Online Library
Tumor necrosis factor (TNF)‐α‐induced hepatocyte apoptosis is implicated in a wide range
of liver diseases including viral hepatitis, alcoholic hepatitis, ischemia/reperfusion liver
injury, and fulminant hepatic failure. TNF‐α exerts a variety of effects that are mediated
mainly by TNF‐receptor 1 (TNF‐R1) in cell death. The activation of TNF‐R1 leads to the
activation of multiple apoptotic pathways involving the activation of the pro‐death Bcl‐2
family proteins, reactive oxygen species, C‐Jun NH2‐terminal kinase, cathepsin B, acidic …
Abstract
Tumor necrosis factor (TNF)‐α‐induced hepatocyte apoptosis is implicated in a wide range of liver diseases including viral hepatitis, alcoholic hepatitis, ischemia/reperfusion liver injury, and fulminant hepatic failure. TNF‐α exerts a variety of effects that are mediated mainly by TNF‐receptor 1 (TNF‐R1) in cell death. The activation of TNF‐R1 leads to the activation of multiple apoptotic pathways involving the activation of the pro‐death Bcl‐2 family proteins, reactive oxygen species, C‐Jun NH2‐terminal kinase, cathepsin B, acidic sphingomyelinase and neutral sphingomyelinase. These pathways are closely interlinked and mainly act on mitochondria, which release the apoptogenic factors and other events, resulting in apoptosis. This article reviews the recent progress in the molecular mechanisms of TNF‐α‐induced apoptosis in hepatocytes, and discusses how these molecular findings are shaping our understanding of the pathogenesis of liver diseases and our strategy to develop novel therapeutics.
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