Targeted redox inhibition of protein phosphatase 1 by Nox4 regulates eIF2α‐mediated stress signaling. (7th January 2016)

• Record Type: Journal Article
• 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; Schröder, 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
• Is Part Of: EMBO journal. Volume 35:Number 3(2016)
• Page Start: 319
• Page End: 334
• Publication Date: 2016-01-07
• Subjects: eIF2α -- metal center -- Nox4 -- protein phosphatase -- redox signaling; Molecular biology -- Periodicals; 572.805
• DOI: 10.15252/embj.201592394
• Languages: English
• ISSNs: 0261-4189

Abstract

Abstract: Phosphorylation of translation initiation factor 2α (eIF2α) 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 eIF2α 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 eIF2α 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 eIF2α phosphorylation to protect tissues under stress. Synopsis: Protein unfolding stress leads to eIF2α 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, eIF2α 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 eIF2α phosphorylation and ATF4 levels. Nox4 enhances cell and organ survival during stress via this pathway. Abstract : Protein unfolding stress leads to eIF2α 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.