Cloned (Comment) | Organism |
---|---|
recombinant expression of wild-type active NS3 and NS3 mutants in LX-2 cells, real-time PCR expression analysis. Protease competent NS3 has a significant fibrogenic impact in LX-2 cells when compared to protease defective NS3 or GFP control plasmids. The expression of miR-122 is downregulated in both versions of the cells transfected with NS3 plasmids irrespective of protease function, impact of protease competent NS3 and protease defective TNS3 on TGF-beta production from LX-2 cells, overview | Hepacivirus C |
Protein Variants | Comment | Organism |
---|---|---|
additional information | generation of mutated non-structural proteins 3 (NS3) | Hepacivirus C |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Hepacivirus C | - |
HCV | - |
Synonyms | Comment | Organism |
---|---|---|
NS3 protease | - |
Hepacivirus C |
NS3 protein | - |
Hepacivirus C |
General Information | Comment | Organism |
---|---|---|
malfunction | protease competent NS3 has a significant fibrogenic impact in expressing LX-2 cells when compared to protease defective NS3 or GFP control plasmids | Hepacivirus C |
physiological function | possible role of NS3 protease activity of hepatitis C virus in fibrogenesis and miR-122 expression in hepatic stellate cells. Various roles of hepatitis C virus (HCV) NS3 protein in viral pathogenesis are emphasized, especially in the progression of fibrosis and tumors. The expression of miR-122 is downregulated in LX-2 cells transfected with NS3 plasmids, encoding active or defective NS3s, irrespective of protease function. The protease function of NS3 protein is a crucial factor for the induction of hepatic fibrosis but it does not play a complete role in the expression of miR-122. The proteolytically active NS3 protein upregulates TGF-beta1 production | Hepacivirus C |