Hepatitis C virus infection sensitizes human hepatocytes to TRAIL-induced apoptosis in a caspase 9-dependent manner

L Lan, S Gorke, SJ Rau, MB Zeisel, E Hildt… - The Journal of …, 2008 - journals.aai.org
L Lan, S Gorke, SJ Rau, MB Zeisel, E Hildt, K Himmelsbach, M Carvajal-Yepes, R Huber…
The Journal of Immunology, 2008journals.aai.org
Apoptosis of infected cells represents a key host defense mechanism against viral infections.
The impact of apoptosis on the elimination of hepatitis C virus (HCV)-infected cells is poorly
understood. The TRAIL has been implicated in the death of liver cells in hepatitis-infected
but not in normal liver cells. To determine the impact of TRAIL on apoptosis of virus-infected
host cells, we studied TRAIL-induced apoptosis in a tissue culture model system for HCV
infection. We demonstrated that HCV infection sensitizes primary human hepatocytes and …
Abstract
Apoptosis of infected cells represents a key host defense mechanism against viral infections. The impact of apoptosis on the elimination of hepatitis C virus (HCV)-infected cells is poorly understood. The TRAIL has been implicated in the death of liver cells in hepatitis-infected but not in normal liver cells. To determine the impact of TRAIL on apoptosis of virus-infected host cells, we studied TRAIL-induced apoptosis in a tissue culture model system for HCV infection. We demonstrated that HCV infection sensitizes primary human hepatocytes and Huh7. 5 hepatoma cells to TRAIL induced apoptosis in a dose-and time-dependent manner. Mapping studies identified the HCV nonstructural proteins as key mediators of sensitization to TRAIL. Using a panel of inhibitors targeting different apoptosis pathways, we demonstrate that sensitization to TRAIL is caspase-9 dependent and mediated in part via the mitochondrial pathway. Sensitization of hepatocytes to TRAIL-induced apoptosis by HCV infection represents a novel antiviral host defense mechanism that may have important implications for the pathogenesis of HCV infection and may contribute to the elimination of virus-infected hepatocytes.
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