Endoplasmic Reticulum Oxidative Stress Promotes Glutathione-Dependent Oxidation of Collagen-1A1 and Promotes Lung Fibroblast Activation

Am J Respir Cell Mol Biol. 2024 Nov;71(5):589-602. doi: 10.1165/rcmb.2023-0379OC.

Abstract

Changes in the oxidative (redox) environment accompany idiopathic pulmonary fibrosis (IPF). S-glutathionylation of reactive protein cysteines is a post-translational event that transduces oxidant signals into biological responses. We recently demonstrated that increases in S-glutathionylation promote pulmonary fibrosis, which was mitigated by the deglutathionylating enzyme glutaredoxin (GLRX). However, the protein targets of S-glutathionylation that promote fibrogenesis remain unknown. In the present study we addressed whether the extracellular matrix is a target for S-glutathionylation. We discovered increases in COL1A1 (collagen 1A1) S-glutathionylation (COL1A1-SSG) in lung tissues from subjects with IPF compared with control subjects in association with increases in ERO1A (endoplasmic reticulum [ER] oxidoreductin 1) and enhanced oxidation of ER-localized PRDX4 (peroxiredoxin 4), reflecting an increased oxidative environment of the ER. Human lung fibroblasts exposed to TGFB1 (transforming growth factor-β1) show increased secretion of COL1A1-SSG. Pharmacologic inhibition of ERO1A diminished the oxidation of PRDX4, attenuated COL1A1-SSG and total COL1A1 concentrations, and dampened fibroblast activation. Absence of Glrx enhanced COL1A1-SSG and overall COL1A1 secretion and promoted the activation of mechanosensing pathways. Remarkably, COL1A1-SSG resulted in marked resistance to collagenase degradation. Compared with COL1, lung fibroblasts plated on COL1-SSG proliferated more rapidly and increased the expression of genes encoding extracellular matrix crosslinking enzymes and genes linked to mechanosensing pathways. Overall, these findings suggest that glutathione-dependent oxidation of COL1A1 occurs in settings of IPF in association with enhanced ER oxidative stress and may promote fibrotic remodeling because of increased resistance to collagenase-mediated degradation and fibroblast activation.

Keywords: glutaredoxin; glutathionylation; idiopathic pulmonary fibrosis; mechanosensing; redox.

MeSH terms

  • Collagen Type I* / metabolism
  • Collagen Type I, alpha 1 Chain*
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum Stress
  • Fibroblasts* / metabolism
  • Glutaredoxins / genetics
  • Glutaredoxins / metabolism
  • Glutathione* / metabolism
  • Humans
  • Idiopathic Pulmonary Fibrosis* / metabolism
  • Idiopathic Pulmonary Fibrosis* / pathology
  • Lung* / metabolism
  • Lung* / pathology
  • Membrane Glycoproteins
  • Oxidation-Reduction*
  • Oxidative Stress*
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Peroxiredoxins
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Collagen Type I, alpha 1 Chain
  • Collagen Type I
  • Glutathione
  • Glutaredoxins
  • ERO1A protein, human
  • COL1A1 protein, human
  • PRDX4 protein, human
  • Transforming Growth Factor beta1
  • Oxidoreductases
  • Membrane Glycoproteins
  • Peroxiredoxins