The HP1γ epigenetic silencer dampens IFN-γ response at the gut epithelial barrier

Abstract

Interferon gamma (IFN-γ) plays central roles in the pathophysiology of inflammatory bowel disease (IBD), both activating inflammatory responses and immunosuppressive functions. However, the epigenetic mechanisms controlling the expression of IFN-γ responsive genes at the gut epithelial barrier are not well understood. In this study, we identified the epigenetic regulator HP1γ as a transcriptional repressor of the IFN-γ-responsive genes STAT1 (signal transducer and activator of transcription 1) and PD-L1 (Programmed Cell Death Ligand 1). Accordingly, HP1γ gene inactivation in the mouse gut epithelium resulted in an immunopathology with a long-lasting up-regulation of STAT1 and PD-L1. Colon organoids models and in vitro cell lines showed that HP1γ deficiency primed STAT1 and PD-L1 expressions, ultimately sensitizing epithelial cells to IFN-γ stimulation. Chromatin immunoprecipitation experiments suggest that HP1 promoter tethering is involved in the silencing of gene expression. Overall, these results identify HP1γ as an epigenetic silencing pathway controlling the IFN-γ response at the epithelial barrier.

HP1γ Prevents Activation of the cGAS/STING Pathway by Preserving Nuclear Envelope and Genomic Integrity in Colon Adenocarcinoma Cells

“…[40,41]. Thus, aside from its function as an epigenetic silencer of inflammatory genes [42], HP1γ may also exert anti-inflammatory properties by preserving from a deleterious cytoplasmic DNA response. We next analyzed the expression levels of TGFβ, a protein downstream of STING and the type-I interferon (IFN) family.…”

“…[ 40 , 41 ]. Thus, aside from its function as an epigenetic silencer of inflammatory genes [ 42 ], HP1γ may also exert anti-inflammatory properties by preserving from a deleterious cytoplasmic DNA response.…”