Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
Max Planck Florida Institute for Neuroscience, Jupiter, United States.
Elife. 2018 Feb 8;7:e33273. doi: 10.7554/eLife.33273.
Stress can be a motivational force for decisive action and adapting to novel environment; whereas, exposure to chronic stress contributes to the development of depression and anxiety. However, the molecular mechanisms underlying stress-responsive behaviors are not fully understood. Here, we identified the orphan receptor GPR158 as a novel regulator operating in the prefrontal cortex (PFC) that links chronic stress to depression. GPR158 is highly upregulated in the PFC of human subjects with major depressive disorder. Exposure of mice to chronic stress also increased GPR158 protein levels in the PFC in a glucocorticoid-dependent manner. Viral overexpression of GPR158 in the PFC induced depressive-like behaviors. In contrast GPR158 ablation, led to a prominent antidepressant-like phenotype and stress resiliency. We found that GPR158 exerts its effects via modulating synaptic strength altering AMPA receptor activity. Taken together, our findings identify a new player in mood regulation and introduce a pharmacological target for managing depression.
压力可以成为采取果断行动和适应新环境的动力;然而,长期暴露于压力会导致抑郁和焦虑的发生。然而,压力反应行为的分子机制尚不完全清楚。在这里,我们鉴定出孤儿受体 GPR158 是一种在大脑前额叶皮层(PFC)中起作用的新型调节因子,它将慢性应激与抑郁联系起来。GPR158 在患有重度抑郁症的人类受试者的 PFC 中高度上调。慢性应激暴露也以糖皮质激素依赖性方式增加了 PFC 中的 GPR158 蛋白水平。病毒过表达 GPR158 在 PFC 中诱导出类似抑郁的行为。相反,GPR158 缺失导致明显的抗抑郁样表型和应激弹性。我们发现 GPR158 通过调节 AMPA 受体活性来改变突触强度发挥作用。总之,我们的发现确定了一种新的调节情绪的分子,为治疗抑郁症提供了一个药理学靶点。