| Literature DB >> 25716320 |
Ana Tomasovic1, Nina Kurrle1, Duran Sürün1, Juliana Heidler1, Koraljka Husnjak2, Ina Poser3, Frank Schnütgen1, Susan Scheibe4, Michael Seimetz4, Peter Jaksch5, Anthony Hyman3, Norbert Weissmann4, Harald von Melchner6.
Abstract
We recently identified the antioxidant protein Sestrin 2 (Sesn2) as a suppressor of platelet-derived growth factor receptor β (Pdgfrβ) signaling and Pdgfrβ signaling as an inducer of lung regeneration and injury repair. Here, we identified Sesn2 and the antioxidant gene inducer nuclear factor erythroid 2-related factor 2 (Nrf2) as positive regulators of proteasomal function. Inactivation of Sesn2 or Nrf2 induced reactive oxygen species-mediated proteasomal inhibition and Pdgfrβ accumulation. Using bacterial artificial chromosome (BAC) transgenic HeLa and mouse embryonic stem cells stably expressing enhanced green fluorescent protein-tagged Sesn2 at nearly endogenous levels, we also showed that Sesn2 physically interacts with 2-Cys peroxiredoxins and Nrf2 albeit under different reductive conditions. Overall, we characterized a novel, redox-sensitive Sesn2/Pdgfrβ suppressor pathway that negatively interferes with lung regeneration and is up-regulated in the emphysematous lungs of patients with chronic obstructive pulmonary disease (COPD).Entities:
Keywords: Chronic Obstructive Pulmonary Disease (COPD); Nuclear Factor 2 (Erythroid-derived 2-like Factor) (NFE2L2) (Nrf2); Peroxiredoxin; Proteasome; Reactive Oxygen Species (ROS)
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Year: 2015 PMID: 25716320 PMCID: PMC4392273 DOI: 10.1074/jbc.M114.632133
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157