AI Article Synopsis

  • Emerging research highlights the significant role of Nox1-generated reactive oxygen species (ROS) in regulating various cellular processes, although specific targets of Nox1 are still not well understood.
  • The study identified ERp72, a protein with TRX homology domains, as a direct target of Nox1-induced oxidation, which leads to decreased reductase activity of ERp72.
  • The findings show that Nox1 interacts with ERp72 at the plasma membrane, suggesting a functional partnership that influences redox-sensitive signaling pathways within cells.

Article Abstract

Emerging evidence indicates that Nox (NADPH oxidase) 1-generated ROS (reactive oxygen species) play critical regulatory roles in various cellular processes, yet little is known of direct targets for the oxidase. In the present study we show that one of the proteins selectively oxidized in response to Nox1-generated ROS was ERp72 (endoplasmic reticulum protein 72 kDa) with TRX (thioredoxin) homology domains. Oxidation of ERp72 by Nox1 resulted in an inhibition of its reductase activity. EGF treatment of cells stimulated the Nox1 activity and the activated Nox1 subsequently mediated EGF-induced suppression of the ERp72 reductase activity. Co-immunoprecipitation, GST (glutathione transferase) pulldown assays and mutational analysis, indicated that Nox1 associates with ERp72, which involves its N-terminus encompassing a Ca(2+)-binding site and the first TRX-like motif. Furthermore, confocal microscopy showed co-localization between Nox1 and ERp72 at the plasma membrane. These results suggest that Nox1 functionally associates with ERp72, regulating redox-sensitive signalling pathways in a cellular context.

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http://dx.doi.org/10.1042/BJ20071259DOI Listing

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