Vitamin D receptor and Jak-STAT signaling crosstalk results in calcitriol-mediated increase of hepatocellular response to IFN-α

• Published in: The Journal of immunology (1950) 2014-06, Vol.192 (12), p.6037-6044
• Main Authors: Lange, Christian M, Gouttenoire, Jérôme, Duong, François H T, Morikawa, Kenichi, Heim, Markus H, Moradpour, Darius
• Format: Article
• Language: English
• Subjects: Calcitriol - pharmacology; Cell Line; Gene Expression Regulation - drug effects; Gene Expression Regulation - genetics; Gene Expression Regulation - immunology; Hepacivirus - physiology; Hepatitis C - drug therapy; Hepatitis C - genetics; Hepatitis C - immunology; Hepatitis C - pathology; Hepatitis C virus; Humans; Interferon-alpha - pharmacology; Janus Kinases - genetics; Janus Kinases - immunology; Phosphorylation - drug effects; Phosphorylation - genetics; Phosphorylation - immunology; Receptors, Calcitriol - genetics; Receptors, Calcitriol - immunology; Signal Transduction - drug effects; Signal Transduction - genetics; Signal Transduction - immunology; STAT1 Transcription Factor - genetics; STAT1 Transcription Factor - immunology; Virus Replication - drug effects; Virus Replication - immunology; Vitamins - pharmacology
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1302296

Recent clinical research suggests a role for vitamin D in the response to IFN-α-based therapy of chronic hepatitis C. Therefore, we aimed to explore the underlying mechanisms in vitro. Huh-7.5 cells harboring subgenomic hepatitis C virus (HCV) replicons or infected with cell culture-derived HCV were exposed to bioactive 1,25-dihydroxyvitamin D3 (calcitriol) with or without IFN-α. In these experiments, calcitriol alone had no effect on the HCV life cycle. However, calcitriol enhanced the inhibitory effect of IFN-α on HCV replication. This effect was based on a calcitriol-mediated increase of IFN-α-induced gene expression. Further mechanistic studies revealed a constitutive inhibitory interaction between the inactive vitamin D receptor (VDR) and Stat1, which was released upon stimulation with calcitriol and IFN-α. As a consequence, IFN-α-induced binding of phosphorylated Stat1 to its DNA target sequences was enhanced by calcitriol. Importantly, and in line with these observations, silencing of the VDR resulted in an enhanced hepatocellular response to IFN-α. Our findings identify the VDR as a novel suppressor of IFN-α-induced signaling through the Jak-STAT pathway.