Dynamic regulation of canonical TGFβ signalling by endothelial transcription factor ERG protects from liver fibrogenesis
Research output: Contribution to journal › Article › peer-review
- Imperial College London
- University of Birmingham
The role of the endothelium in protecting from chronic liver disease and TGFβ-mediated fibrosis remains unclear. Here we describe how the endothelial transcription factor ETS-related gene (ERG) promotes liver homoeostasis by controlling canonical TGFβ-SMAD signalling, driving the SMAD1 pathway while repressing SMAD3 activity. Molecular analysis shows that ERG binds to SMAD3, restricting its access to DNA. Ablation of ERG expression results in endothelial-to-mesenchymal transition (EndMT) and spontaneous liver fibrogenesis in EC-specific constitutive hemi-deficient (Erg cEC-Het ) and inducible homozygous deficient mice (Erg iEC-KO ), in a SMAD3-dependent manner. Acute administration of the TNF-α inhibitor etanercept inhibits carbon tetrachloride (CCL4)-induced fibrogenesis in an ERG-dependent manner in mice. Decreased ERG expression also correlates with EndMT in tissues from patients with end-stage liver fibrosis. These studies identify a pathogenic mechanism where loss of ERG causes endothelial-dependent liver fibrogenesis via regulation of SMAD2/3. Moreover, ERG represents a promising candidate biomarker for assessing EndMT in liver disease.The transcription factor ERG is key to endothelial lineage specification and vascular homeostasis. Here the authors show that ERG balances TGFβ signalling through the SMAD1 and SMAD3 pathways, protecting the endothelium from endothelial-to-mesenchymal transition and consequent liver fibrosis in mice via a SMAD3-dependent mechanism.
|Publication status||Published - 12 Oct 2017|
- Animals, Carbon Tetrachloride, Cells, Cultured, Down-Regulation, End Stage Liver Disease, Endothelial Cells, Epithelial-Mesenchymal Transition, Etanercept, Female, Fibrosis, Human Umbilical Vein Endothelial Cells, Humans, Liver, Liver Cirrhosis, Biliary, Liver Cirrhosis, Experimental, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Oncogene Proteins, Signal Transduction, Smad1 Protein, Smad2 Protein, Smad3 Protein, Transcriptional Regulator ERG, Transforming Growth Factor beta, Tumor Necrosis Factor-alpha, Up-Regulation, Journal Article, Research Support, Non-U.S. Gov't