Institute of Life Sciences, Key Laboratory of Developmental Genes and Human Diseases, Southeast University, Nanjing 210096, China.
Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, JS 226001, China.
Sci Rep. 2016 Dec 1;6:38246. doi: 10.1038/srep38246.
Neurexins are cell adhesion molecules involved in synaptic formation and synaptic transmission. Mutations in neurexin genes are linked to autism spectrum disorders (ASDs), which are frequently associated with sleep problems. However, the role of neurexin-mediated synaptic transmission in sleep regulation is unclear. Here, we show that lack of the Drosophila α-neurexin homolog significantly reduces the quantity and quality of nighttime sleep and impairs sleep homeostasis. We report that neurexin expression in Drosophila mushroom body (MB) αβ neurons is essential for nighttime sleep. We demonstrate that reduced nighttime sleep in neurexin mutants is due to impaired αβ neuronal output, and show that neurexin functionally couples calcium channels (Cac) to regulate synaptic transmission. Finally, we determine that αβ surface (αβ) neurons release both acetylcholine and short neuropeptide F (sNPF), whereas αβ core (αβ) neurons release sNPF to promote nighttime sleep. Our findings reveal that neurexin regulates nighttime sleep by mediating the synaptic transmission of αβ neurons. This study elucidates the role of synaptic transmission in sleep regulation, and might offer insights into the mechanism of sleep disturbances in patients with autism disorders.
神经连接蛋白是参与突触形成和突触传递的细胞粘附分子。神经连接蛋白基因的突变与自闭症谱系障碍(ASD)有关,而 ASD 通常与睡眠问题有关。然而,神经连接蛋白介导的突触传递在睡眠调节中的作用尚不清楚。在这里,我们发现 Drosophila α-neurexin 同源物的缺失显著减少了夜间睡眠的数量和质量,并损害了睡眠稳态。我们报告说,Drosophila 蘑菇体(MB)αβ 神经元中的神经连接蛋白表达对于夜间睡眠是必需的。我们证明了神经连接蛋白突变体中夜间睡眠减少是由于αβ 神经元输出受损所致,并表明神经连接蛋白通过功能性偶联钙通道(Cac)来调节突触传递。最后,我们确定αβ 表面(αβ)神经元释放乙酰胆碱和短神经肽 F(sNPF),而αβ 核心(αβ)神经元释放 sNPF 以促进夜间睡眠。我们的研究结果表明,神经连接蛋白通过调节αβ 神经元的突触传递来调节夜间睡眠。本研究阐明了突触传递在睡眠调节中的作用,可能为自闭症患者睡眠障碍的机制提供了一些启示。