Activating transcription factor 4 and CCAAT/enhancer-binding protein-β negatively regulate the mammalian target of rapamycin via Redd1 expression in response to oxidative and endoplasmic reticulum stress

• Published in: Free radical biology & medicine Vol. 46; no. 8; pp. 1158 - 1167
• Main Authors: Jin, Hyeon-Ok, Seo, Sung-Keum, Woo, Sang-Hyeok, Kim, Eun-Sung, Lee, Hyung-Chahn, Yoo, Doo-Hyun, An, Sungkwan, Choe, Tae-Boo, Lee, Su-Jae, Hong, Seok-Il, Rhee, Chang-Hun, Kim, Jong-Il, Park, In-Chul
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.04.2009
• Subjects: Activating Transcription Factor 4 - genetics; Activating Transcription Factor 4 - metabolism; Activating Transcription Factor 4 - physiology; ATF4; C/EBP-β; CCAAT-Enhancer-Binding Protein-beta - physiology; Endoplasmic Reticulum; ER stress; Feedback, Physiological; HeLa Cells; Humans; Hydrogen Peroxide - metabolism; mTOR; Oxidative Stress; Protein Kinases - genetics; Protein Kinases - metabolism; Redd1/RTP801; RNA, Small Interfering - genetics; Signal Transduction; Sirolimus - metabolism; TOR Serine-Threonine Kinases; Transcription Factors - genetics; Transcription Factors - metabolism; Transcriptional Activation; ER stress; mTOR; Oxidative stress; Redd1/RTP801; C/EBP-β; ATF4
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2009.01.015

Regulation of mRNA translation in mammalian cells involves the coordinated control of mammalian target of rapamycin (mTOR) signaling. At present, limited information is available on the potential relevance of mTOR regulation, although translation inhibition during oxidative and endoplasmic reticulum (ER) stress is clearly important. In this study, we show that activating transcription factor 4 (ATF4) and CCAAT/enhancer-binding protein-β (C/EBP-β) negatively regulate mTOR via Redd1 expression in response to oxidative and ER stress. Oxidative and ER stress conditions induce rapid and significant activation of ATF4 downstream of eIF2α phosphorylation, which is responsible for Redd1 expression. In our experiment, overexpression of ATF4 was associated with reduced mTOR activity via Redd1 expression, whereas suppression of ATF4 levels with small interfering RNA led to the recovery of decreased mTOR activity mediated by downregulation of Redd1 during oxidative and ER stress. We additionally identified Redd1 as a downstream effector of C/EBP-β stimulated by ATF4 activated under the stress conditions examined. RNA interference studies provided further evidence of the requirement of C/EBP-β for Redd1 expression. We conclude that the Redd1 gene is transactivated by the ATF4 and C/EBP family of transcription factors, leading to mTOR inhibition in response to oxidative and ER stress.