PLAC8-Mediated Activation of NOX4 Signalling Restores Angiogenic Function of Endothelial Colony-Forming Cells in Experimental Hypoxia

Cells. 2023 Sep 6;12(18):2220. doi: 10.3390/cells12182220.

Abstract

Ischaemic cardiovascular disease is associated with tissue hypoxia as a significant determinant of angiogenic dysfunction and adverse remodelling. While cord blood-derived endothelial colony-forming cells (CB-ECFCs) hold clear therapeutic potential due to their enhanced angiogenic and proliferative capacity, their impaired functionality within the disease microenvironment represents a major barrier to clinical translation. The aim of this study was to define the specific contribution of NOX4 NADPH oxidase, which we previously reported as a key CB-ECFC regulator, to hypoxia-induced dysfunction and its potential as a therapeutic target. CB-ECFCs exposed to experimental hypoxia demonstrated downregulation of NOX4-mediated reactive oxygen species (ROS) signalling linked with a reduced tube formation, which was partially restored by NOX4 plasmid overexpression. siRNA knockdown of placenta-specific 8 (PLAC8), identified by microarray analysis as an upstream regulator of NOX4 in hypoxic versus normoxic CB-ECFCs, enhanced tube formation, NOX4 expression and hydrogen peroxide generation, and induced several key transcription factors associated with downstream Nrf2 signalling. Taken together, these findings indicated that activation of the PLAC8-NOX4 signalling axis improved CB-ECFC angiogenic functions in experimental hypoxia, highlighting this pathway as a potential target for protecting therapeutic cells against the ischaemic cardiovascular disease microenvironment.

Keywords: NOX4 NADPH oxidase; angiogenesis; endothelial colony-forming cells; hypoxia; placenta-specific 8; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Hypoxia*
  • Endothelial Cells / metabolism
  • Fetal Blood / cytology
  • Fetal Blood / metabolism
  • Humans
  • Hydrogen Peroxide / metabolism
  • NADPH Oxidase 4 / genetics
  • NADPH Oxidase 4 / metabolism
  • NF-E2-Related Factor 2 / metabolism
  • Neovascularization, Physiologic* / genetics
  • Reactive Oxygen Species / metabolism
  • Signal Transduction*

Substances

  • Hydrogen Peroxide
  • NADPH Oxidase 4
  • NF-E2-Related Factor 2
  • NOX4 protein, human
  • Reactive Oxygen Species