The inflammatory cytokine interferon‐gamma inhibits sortilin‐1 expression in hepatocytes via the JAK/STAT pathway

摘要

Abstract Sortilin‐1, a receptor of the VPS10p family, has been associated with cardiovascular disease in genome‐wide association studies. It is implicated in lipoprotein metabolism, secretion of proprotein convertase subtilisin/kexin type 9 (PCSK9) and secretion of inflammatory cytokines. However, its own regulation remains unclear. Chronic inflammation is a hallmark of atherosclerosis and the absence of regulatory T (Treg) cells is associated with reduced protein expression of sortilin‐1 in the liver. Therefore, we postulated that mediator(s) of inflammation known to be downregulated by Treg cells may modulate sortilin‐1 expression. In this study, we identify interferon‐gamma (IFN‐γ) as the key inflammatory mediator controlling sortilin‐1 levels. In vitro cultures of murine hepatocytes cell line and in silico experiments showed that the transcription factor Signal transducer and activator of transcription 1 was activated and bound to the Sort‐1 gene upon IFN‐γ treatment. This reduced the expression of sortilin‐1, while disrupting the IFN‐γ signaling pathway prevented the effect. These data unravel an intricate mechanism by which inflammation modulates receptors involved in lipoprotein turnover.