Institute of Animal Developmental and Molecular Biology, Heinrich Heine University, Düsseldorf, Germany.
PLoS One. 2019 Feb 7;14(2):e0211937. doi: 10.1371/journal.pone.0211937. eCollection 2019.
Initially, the function of the fat mass and obesity associated (Fto) gene seemed to be primarily the regulation of the body weight. Here we show that loss of Fto results in a hyperactivation of the hypothalamic-pituitary-adrenal (HPA) axis. In consequence, Fto-/- mice display an anxiety-like behavior and impairments in working memory. Furthermore, differentiation of neurons is affected in the hippocampus. As a cause of these impairments we identified a processing defect of the neurotrophin BDNF which is most likely the result of a reduced expression of MMP-9. Therefore, we propose FTO as a possible new target to develop novel approaches for the treatment of diseases associated with hippocampal disorders. In parallel, we also would like to make the point that any anti-obesity therapy via blocking FTO function can have negative effects on the proper function of the hippocampus.
最初,脂肪质量和肥胖相关(Fto)基因的功能似乎主要是调节体重。在这里,我们表明 Fto 的缺失会导致下丘脑-垂体-肾上腺(HPA)轴的过度激活。结果,Fto-/- 小鼠表现出类似焦虑的行为和工作记忆障碍。此外,海马体中的神经元分化受到影响。我们发现作为这些损伤的一个原因,神经营养因子 BDNF 的加工缺陷很可能是由于 MMP-9 的表达减少所致。因此,我们提出 FTO 作为一种可能的新靶点,以开发治疗与海马障碍相关疾病的新方法。同时,我们也想指出,任何通过阻断 FTO 功能的抗肥胖治疗都可能对海马体的正常功能产生负面影响。