TY - JOUR T1 - Bromodomain and extra-terminal (BET) proteins regulate antioxidant gene expression JF - European Respiratory Journal JO - Eur Respir J VL - 42 IS - Suppl 57 SP - 3514 AU - Charalambos Michaeloudes AU - Nicolas Mercado AU - Peter J. Barnes AU - Ian M. Adcock AU - Kian Fan Chung Y1 - 2013/09/01 UR - http://erj.ersjournals.com/content/42/Suppl_57/3514.abstract N2 - Background: Oxidative stress, a key pathogenic factor in COPD, arises due to reactive oxygen species (ROS) accumulation and defective antioxidant defences in the lungs. The latter is partly due to acetylation of the antioxidant gene activator nuclear factor E2-related factor 2 (Nrf2). Bromodomain and extra-terminal (BET) proteins regulate gene transcription by binding to acetylated proteins and recruiting transcriptional regulators to gene promoters. Their role in antioxidant gene regulation is unknown. Aims & Objectives: Determine the role of BET proteins in antioxidant gene expression in human primary airway smooth muscle cells (ASMCs) and THP1 monocytic cells. Methods: BET proteins were inhibited using the selective inhibitor (+) - JQ1 [JQ1]. mRNA and protein expression was determined by real-time PCR and western blotting, respectively. Results: In ASMCs, JQ1 (50-1000nM) increased the mRNA of Nrf2-mediated antioxidants haem oxygenase (HO)-1 (∼5-fold; p<0.05), NADPH: quinone oxidoreductase 1 (NQO1) (∼6-fold; p<0.05) and GCL catalytic subunit (GCLC) (∼4-fold; p<0.05), in a concentration-dependent manner. The up-regulation of HO-1 (∼3-fold; p<0.05), NQO1 (∼2.5-fold; p<0.05) and GCLC (∼2-fold; p<0.05) mRNA by JQ1 (300nM) occurred 8-24hrs post-treatment. Concomitantly, JQ1 (300nM) increased Nrf2 mRNA (∼1.8-fold; p<0.01) and protein (∼3-fold; p<0.05), and reduced the expression of the Nrf2 inhibitor Kelch-like ECH-associated protein 1 (Keap1). JQ1 had the same effect in THP1 cells. Conclusions: BET proteins may augment antioxidant defences and prevent oxidative stress in addition to their known anti-inflammatory and anti-proliferative actions. They have potential as novel therapeutic targets in COPD. ER -