Targeted redox inhibition of protein phosphatase 1 by Nox4 regulates eIF2[alpha]-mediated stress signaling

• Published in: The EMBO journal Vol. 35; no. 3; p. 319
• Main Authors: Santos, Celio XC, Hafstad, Anne D, Beretta, Matteo, Zhang, Min, Molenaar, Chris, Kopec, Jola, Fotinou, Dina, Murray, Thomas V, Cobb, Andrew M, Martin, Daniel, Zeh Silva, Maira, Anilkumar, Narayana, Schroder, Katrin, Shanahan, Catherine M, Brewer, Alison C, Brandes, Ralf P, Blanc, Eric, Parsons, Maddy, Belousov, Vsevelod, Cammack, Richard, Hider, Robert C, Steiner, Roberto A, Shah, Ajay M
• Format: Journal Article
• Language: English
• Published: Heidelberg Blackwell Publishing Ltd 01.02.2016
• Subjects: Endoplasmic reticulum; Inactivation; Kinases; Metals; Oxidation; Phosphatase; Phosphorylation; Protein synthesis; Proteins; Survival
• ISSN: 0261-4189; 1460-2075
• DOI: 10.15252/embj.201592394

Phosphorylation of translation initiation factor 2[alpha] (eIF2[alpha]) attenuates global protein synthesis but enhances translation of activating transcription factor 4 (ATF4) and is a crucial evolutionarily conserved adaptive pathway during cellular stresses. The serine-threonine protein phosphatase 1 (PP1) deactivates this pathway whereas prolonging eIF2[alpha] phosphorylation enhances cell survival. Here, we show that the reactive oxygen species-generating NADPH oxidase-4 (Nox4) is induced downstream of ATF4, binds to a PP1-targeting subunit GADD34 at the endoplasmic reticulum, and inhibits PP1 activity to increase eIF2[alpha] phosphorylation and ATF4 levels. Other PP1 targets distant from the endoplasmic reticulum are unaffected, indicating a spatially confined inhibition of the phosphatase. PP1 inhibition involves metal center oxidation rather than the thiol oxidation that underlies redox inhibition of protein tyrosine phosphatases. We show that this Nox4-regulated pathway robustly enhances cell survival and has a physiologic role in heart ischemia-reperfusion and acute kidney injury. This work uncovers a novel redox signaling pathway, involving Nox4-GADD34 interaction and a targeted oxidative inactivation of the PP1 metal center, that sustains eIF2[alpha] phosphorylation to protect tissues under stress. Synopsis Protein unfolding stress leads to eIF2[alpha] phosphorylation, which is counteracted by protein phosphatase 1 (PP1). This study shows that ROS-generating NADPH oxidase-4 inactivates PP1 at the ER via metal center oxidation, allowing for an enhanced stress signaling response and cell survival. During cellular stresses, eIF2[alpha] phosphorylation inhibits protein synthesis but increases ATF4 translation. NADPH oxidase-4 (Nox4) is induced by ATF4 and binds to a PP1-targeting protein, GADD34, to inhibit PP1 specifically at the ER. PP1 inhibition involves metal center oxidation and results in increased eIF2[alpha] phosphorylation and ATF4 levels. Nox4 enhances cell and organ survival during stress via this pathway.