Non-structural 3 protein expression is associated with T cell protein tyrosine phosphatase and viral RNA levels in chronic hepatitis C patients
Autor: | Nogol Rahbin, Lars Frelin, Erwin Daniel Brenndörfer, Matti Sällberg, Rolf Hultcrantz, Soo Aleman |
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Rok vydání: | 2013 |
Předmět: |
Adult
Male viruses Hepatitis C virus Biophysics Hepacivirus Biology Viral Nonstructural Proteins medicine.disease_cause Biochemistry Liver disease Viral life cycle medicine Humans Molecular Biology Liver injury NS3 Protein Tyrosine Phosphatase Non-Receptor Type 2 virus diseases Cell Biology Hepatitis C biochemical phenomena metabolism and nutrition Hepatitis C Chronic Middle Aged Viral Load medicine.disease digestive system diseases Viral replication Liver Immunology RNA Viral Female Viral load |
Zdroj: | Biochemical and biophysical research communications. 433(1) |
ISSN: | 1090-2104 |
Popis: | The hepatitis C virus (HCV) non-structural 3 (NS3) protein plays key roles in both the viral life cycle and in the modulation of intrahepatic signaling and immunity. We recently showed that NS3 cleaves the T cell protein tyrosine phosphatase (TCPTP). To better understand the inactivation of TCPTP in HCV-infected humans, we investigated whether there is an association between TCPTP cleavage, NS3 protein levels and clinical parameters in hepatitis C patients. Liver biopsies were obtained from 69 HCV RNA positive patients with confirmed chronic HCV infection and 16 control patients. Hepatic NS3 and TCPTP protein levels were determined and correlated to viral load or clinical parameters for the severity of liver disease. We found a positive correlation between the viral load and the intrahepatic NS3 protein levels in patients infected with HCV. HCV-infected patients had significantly lower intrahepatic TCPTP levels than non-infected control patients. In HCV-infected patients both intrahepatic NS3 expression and the viral load were inversely correlated with the intrahepatic TCPTP protein levels. Detection of NS3 did not associate with any other clinical parameters such as liver damage, the grade of liver inflammation or fibrosis stage. This is the first study reporting a detailed analysis of HCV NS3 and TCPTP protein levels in the liver. It demonstrates a clear link between HCV viral load, NS3 expression in the liver and intrahepatic TCPTP levels. Thus, the association between TCPTP cleavage and viral replication may have important consequences for the HCV life cycle and HCV-induced liver diseases. |
Databáze: | OpenAIRE |
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