Interferon alfa down-regulates collagen gene transcription and suppresses experimental hepatic fibrosis in mice

• DOI: 10.1053/jhep.2003.50408
• Publication Date: 2003-09-25T18:21:50Z
• Authors: Y Inagaki
• Keywords: Male; 0301 basic medicine; Down-Regulation; Interferon-alpha; Nuclear Proteins; Mice, Transgenic; Liver Cirrhosis, Experimental; Collagen Type I; Rats; 3. Good health; DNA-Binding Proteins; Mice; 03 medical and health sciences; Gene Expression Regulation; Liver; Animals; Collagen; Phosphorylation; Rats, Wistar; Promoter Regions, Genetic; Carbon Tetrachloride; E1A-Associated p300 Protein; Cells, Cultured

The equilibrium between the production and degradation of collagen is rigorously controlled by a number of growth factors and cytokines. Interferon alfa (IFN–α) is now widely used for the treatment of chronic hepatitis C, which can improve serum levels of fibrotic markers and the degree of hepatic fibrosis, not only in patients who responded to therapy but also in those in whom it is ineffective. These findings may suggest that IFN–α possesses direct antifibrotic effects in addition to its antiviral activity. However, in contrast to IFN–γ, which has been shown to suppress collagen gene transcription, little is known about the mechanisms responsible for the antifibrotic effects of IFN–α. Here, we report that IFN–α, when administered into transgenic mice harboring the α2(I) collagen gene (COL1A2) promoter sequence, significantly repressed promoter activation and prevented the progression of hepatic fibrosis induced by carbon tetrachloride injection. Transient transfection assays indicated that IFN–α decreased the steady–state levels of COL1A2 messenger RNA (mRNA) and inhibited basal and TGF–β/Smad3–stimulated COL1A2 transcription in activated hepatic stellate cells (HSC). These inhibitory effects of IFN–α on COL1A2 transcription were exerted through the interaction between phosphorylated Stat1 and p300. Blocking of the IFN–α signal by overexpressing the intracellular domain–deleted IFN receptor increased basal COL1A2 transcription and abolished the inhibitory effects of IFN–α. In conclusion, our results indicate that IFN–α antagonizes the TGF–β/Smad3–stimulated COL1A2 transcription in vitro and suppresses COL1A2 promoter activation in vivo, providing a molecular basis for antifibrotic effects of IFN–α. (Hepatology 2003;38:890-899).