Department of Neuroscience, Brown University, Providence, RI 02912, USA.
Department of Neuroscience, Brown University, Providence, RI 02912, USA.
Neuron. 2018 Dec 5;100(5):1209-1223.e4. doi: 10.1016/j.neuron.2018.10.005. Epub 2018 Oct 25.
Drugs of abuse, like alcohol, modulate gene expression in reward circuits and consequently alter behavior. However, the in vivo cellular mechanisms through which alcohol induces lasting transcriptional changes are unclear. We show that Drosophila Notch/Su(H) signaling and the secreted fibrinogen-related protein Scabrous in mushroom body (MB) memory circuitry are important for the enduring preference of cues associated with alcohol's rewarding properties. Alcohol exposure affects Notch responsivity in the adult MB and alters Su(H) targeting at the dopamine-2-like receptor (Dop2R). Alcohol cue training also caused lasting changes to the MB nuclear transcriptome, including changes in the alternative splicing of Dop2R and newly implicated transcripts like Stat92E. Together, our data suggest that alcohol-induced activation of the highly conserved Notch pathway and accompanying transcriptional responses in memory circuitry contribute to addiction. Ultimately, this provides mechanistic insight into the etiology and pathophysiology of alcohol use disorder.
滥用药物,如酒精,会调节奖励回路中的基因表达,从而改变行为。然而,酒精诱导持久转录变化的体内细胞机制尚不清楚。我们表明,果蝇 Notch/Su(H)信号通路和蘑菇体(MB)记忆回路中的分泌纤维蛋白原相关蛋白 Scabrous 对于与酒精奖赏特性相关的线索的持久偏好很重要。酒精暴露会影响成年 MB 中的 Notch 反应性,并改变 Su(H)在多巴胺-2 样受体(Dop2R)上的靶向。酒精线索训练也会导致 MB 核转录组的持久变化,包括 Dop2R 的可变剪接和新涉及的转录本(如 Stat92E)的变化。总之,我们的数据表明,酒精诱导的高度保守的 Notch 途径的激活以及记忆回路中伴随的转录反应有助于成瘾。最终,这为酒精使用障碍的病因和发病生理学提供了机制上的见解。