An essential role for EROS in redox-dependent endothelial signal transduction

Redox Biol. 2024 Jul:73:103214. doi: 10.1016/j.redox.2024.103214. Epub 2024 May 24.

Abstract

The chaperone protein EROS ("Essential for Reactive Oxygen Species") was recently discovered in phagocytes. EROS was shown to regulate the abundance of the ROS-producing enzyme NADPH oxidase isoform 2 (NOX2) and to control ROS-mediated cell killing. Reactive oxygen species are important not only in immune surveillance, but also modulate physiological signaling responses in multiple tissues. The roles of EROS have not been previously explored in the context of oxidant-modulated cell signaling. Here we show that EROS plays a key role in ROS-dependent signal transduction in vascular endothelial cells. We used siRNA-mediated knockdown and developed CRISPR/Cas9 knockout of EROS in human umbilical vein endothelial cells (HUVEC), both of which cause a significant decrease in the abundance of NOX2 protein, associated with a marked decrease in RAC1, a small G protein that activates NOX2. Loss of EROS also attenuates receptor-mediated hydrogen peroxide (H2O2) and Ca2+ signaling, disrupts cytoskeleton organization, decreases cell migration, and promotes cellular senescence. EROS knockdown blocks agonist-modulated eNOS phosphorylation and nitric oxide (NO) generation. These effects of EROS knockdown are strikingly similar to the alterations in endothelial cell responses that we previously observed following RAC1 knockdown. Proteomic analyses following EROS or RAC1 knockdown in endothelial cells showed that reduced abundance of these two distinct proteins led to largely overlapping effects on endothelial biological processes, including oxidoreductase, protein phosphorylation, and endothelial nitric oxide synthase (eNOS) pathways. These studies demonstrate that EROS plays a central role in oxidant-modulated endothelial cell signaling by modulating NOX2 and RAC1.

Keywords: EROS; Endothelial cells; NOX2; RAC1; Redox signaling; Reductive stress.

MeSH terms

  • Cell Movement
  • Cellular Senescence
  • Gene Knockdown Techniques
  • Human Umbilical Vein Endothelial Cells* / metabolism
  • Humans
  • Hydrogen Peroxide / metabolism
  • NADPH Oxidase 2* / genetics
  • NADPH Oxidase 2* / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type III / genetics
  • Nitric Oxide Synthase Type III / metabolism
  • Oxidation-Reduction*
  • Phosphorylation
  • Reactive Oxygen Species* / metabolism
  • Signal Transduction*
  • rac1 GTP-Binding Protein* / genetics
  • rac1 GTP-Binding Protein* / metabolism

Substances

  • NADPH Oxidase 2
  • rac1 GTP-Binding Protein
  • Reactive Oxygen Species
  • CYBB protein, human
  • RAC1 protein, human
  • Hydrogen Peroxide
  • Nitric Oxide Synthase Type III
  • Nitric Oxide