Mediterranean Research Centre for Molecular Medicine, Team Cellular and Molecular Physiopathology of Obesity and Diabetes, INSERM U 895, F-06204 Nice, France.
J Biol Chem. 2010 Feb 19;285(8):5157-64. doi: 10.1074/jbc.M109.047688. Epub 2009 Dec 8.
REDD1 (regulated in development and DNA damage responses) is essential for the inhibition of mTORC1 (mammalian target of rapamycin complex) signaling pathway in response to hypoxia. REDD1 expression is regulated by many stresses such as hypoxia, oxidative stress, and energy depletion. However, the regulation of REDD1 expression in response to insulin remains unknown. In the present study, we demonstrate that in murine and in human adipocytes, insulin stimulates REDD1 expression. Insulin-induced REDD1 expression occurs through phosphoinositide 3-kinase/mTOR-dependent pathways. Moreover, using echinomycin, a hypoxia-inducible factor 1 (HIF-1) inhibitor, and HIF-1alpha small interfering RNA, we demonstrate that insulin stimulates REDD1 expression only through the transcription factor HIF-1. In conclusion, our study shows that insulin stimulates REDD1 expression in adipocytes.
REDD1(发育和 DNA 损伤反应调节)对于抑制缺氧反应中的 mTORC1(雷帕霉素靶蛋白复合物)信号通路是必需的。REDD1 的表达受到许多应激的调节,如缺氧、氧化应激和能量耗竭。然而,胰岛素对 REDD1 表达的调节仍然未知。在本研究中,我们证明在鼠和人脂肪细胞中,胰岛素刺激 REDD1 的表达。胰岛素诱导的 REDD1 表达是通过磷酸肌醇 3-激酶/mTOR 依赖途径发生的。此外,使用抑制缺氧诱导因子 1(HIF-1)的 echinomycin 和 HIF-1alpha 小干扰 RNA,我们证明胰岛素仅通过转录因子 HIF-1 刺激 REDD1 的表达。总之,我们的研究表明胰岛素刺激脂肪细胞中 REDD1 的表达。