A20 suppresses canonical Smad-dependent fibroblast activation: novel function for an endogenous inflammatory modulator

Arthritis Res Ther. 2016 Oct 3;18(1):216. doi: 10.1186/s13075-016-1118-7.

Abstract

Background: The ubiquitin-editing cytosolic enzyme A20, the major negative regulator of toll-like receptor (TLR)-mediated cellular inflammatory responses, has tight genetic linkage with systemic sclerosis (SSc). Because recent studies implicate endogenous ligand-driven TLR signaling in SSc pathogenesis, we sought to investigate the regulation, role and mechanism of action of A20 in skin fibroblasts.

Method: A20 expression and the effects of forced A20 expression or siRNA-mediated A20 knockdown on fibrotic responses induced by transforming growth factor-ß (TGF-ß) were evaluated was evaluated in explanted human skin fibroblasts. Additionally, A20 regulation by TGF-ß, and by adiponectin, a pleiotropic adipokine with anti-fibrotic activity, was evaluated.

Results: In normal fibroblasts, TGF-ß induced sustained downregulation of A20, and abrogated its TLR4-dependent induction. Forced expression of A20 aborted the stimulation of collagen gene expression and myofibroblast transformation induced by TGF-ß, and disrupted canonical Smad signaling and Smad-dependent transcriptional responses. Conversely, siRNA-mediated knockdown of A20 enhanced the amplitude of fibrotic responses elicited by TGF-ß. Adiponectin, previously shown to block TLR-dependent fibrotic responses, elicited rapid and sustained increase in A20 accumulation in fibroblasts.

Conclusion: These results identify the ubiquitin-editing enzyme A20 as a novel endogenous mechanism for negative regulation of fibrotic response intensity. Systemic sclerosis-associated genetic variants of A20 that cause impaired A20 expression or function, combined with direct suppression of A20 by TGF-ß within the fibrotic milieu, might play a significant functional role in persistence of fibrotic responses, while pharmacological augmentation of A20 inhibitory pathway activity might represent a novel therapeutic strategy.

Keywords: A20; Fibrosis; IL-6; LPS; Systemic sclerosis; TGF-ß; TLR4; TNFAIP3; Type I collagen; adiponectin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Blotting, Western
  • Cells, Cultured
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Fibrosis / metabolism
  • Fibrosis / pathology
  • Fluorescent Antibody Technique
  • Gene Knockdown Techniques
  • Humans
  • Microscopy, Confocal
  • Polymerase Chain Reaction
  • Scleroderma, Systemic / metabolism*
  • Scleroderma, Systemic / pathology
  • Signal Transduction / physiology
  • Skin / metabolism
  • Skin / pathology
  • Smad Proteins / metabolism*
  • Transforming Growth Factor beta / metabolism
  • Tumor Necrosis Factor alpha-Induced Protein 3 / metabolism*

Substances

  • Smad Proteins
  • Transforming Growth Factor beta
  • TNFAIP3 protein, human
  • Tumor Necrosis Factor alpha-Induced Protein 3