Antioxidant, N-acetyl-L-cysteine inhibits the expression of the collagen α2 (I) promoter in the activated human hepatic stellate cell line in the absence as well as the presence of transforming growth factor-β
        Hepatology research : the official journal of the Japan Society of Hepatology Volume 24 Issue 3
        Page 305-315
        
published_at 2002
            Title
        
        Antioxidant, N-acetyl-L-cysteine inhibits the expression of the collagen α2 (I) promoter in the activated human hepatic stellate cell line in the absence as well as the presence of transforming growth factor-β
        
        
    
                
                    Creators
                
                    Kayano Kozo
                
                
            
            
                
                    Creators
                
                    Sakaguchi Eiki
                
                
            
            
            
            
                
                    Creators
                
                    Okita Kiwamu
                
                
            
    
            Creator Keywords
        
            Liver fibrosis
            Hepatic stellate cell
            N-acetyl- -cysteine
            LI90
            COL1A2 promoter
    Although recent studies suggest the inhibitory property of N-acetyl-L-cysteine (NAC) on activation of hepatic stellate cell (HSC), the effects on once-activated HSCs are not well clarified. We investigated the influences of NAC on human-derived once-activated HSC line, LI90 with a focus on the collagen α2 (I) (COL1A2) promoter expression. Plasmid containing whole length of COL1A2 promoter linked to firefly luciferase gene and its various 5′-deletions were transiently transfected to LI90. The luciferase activity was determined with or without 10 mM of NAC in the absence or presence of 1 ng/ml of transforming growth factor (TGF)-β. The effects of NAC on generation of intracellular reactive oxygen species (ROS) in LI90 were also analyzed. As a result, NAC significantly (P<0.05) suppressed the COL1A2 promoter expression in the absence or presence of TGF-β. The expression was much more inhibited when used the deletion containing only AP-1/NF-κB binding sites than that including only three SP-1 binding sites. The ROS production was also comparably inhibited by NAC in both condition. These results indicated NAC suppressed, through its anti-oxidative action, the COL1A2 promoter expression in once-activated HSCs in the absence or presence of TGF-β at least partly by affecting the signal transduction cascade encompassing AP-1/NF-κB activation.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        journal article
    
    
        
            Publishers
        
            Elsevier
    
    
        
            Date Issued
        
        2002
    
    
        
            File Version
        
        Not Applicable (or Unknown)
    
    
        
            Access Rights
        
        metadata only access
    
    
            Relations
        
            
                
                
                [ISSN]1386-6346
            
            
                
                
                [NCID]AA11140867
            
            
            
                [isVersionOf]
                
                [URI]http://www.sciencedirect.com/science/journal/13866346
            
    
