California Institute of Technology, Division of Biology and Biological Engineering, Pasadena, United States.
Elife. 2020 Dec 18;9:e54491. doi: 10.7554/eLife.54491.
Although several sleep-regulating neuronal populations have been identified, little is known about how they interact with each other to control sleep/wake states. We previously identified neuropeptide VF (NPVF) and the hypothalamic neurons that produce it as a sleep-promoting system (Lee et al., 2017). Here we show using zebrafish that -expressing neurons control sleep via the serotonergic raphe nuclei (RN), a hindbrain structure that is critical for sleep in both diurnal zebrafish and nocturnal mice. Using genetic labeling and calcium imaging, we show that -expressing neurons innervate and can activate serotonergic RN neurons. We also demonstrate that chemogenetic or optogenetic stimulation of expressing neurons induces sleep in a manner that requires NPVF and serotonin in the RN. Finally, we provide genetic evidence that NPVF acts upstream of serotonin in the RN to maintain normal sleep levels. These findings reveal a novel hypothalamic-hindbrain neuronal circuit for sleep/wake control.
尽管已经确定了几个调节睡眠的神经元群体,但对于它们如何相互作用来控制睡眠/觉醒状态知之甚少。我们之前发现神经肽 VF(NPVF)和产生它的下丘脑神经元是一种促进睡眠的系统(Lee 等人,2017)。在这里,我们使用斑马鱼表明表达神经元通过 5-羟色胺能中缝核(RN)控制睡眠,这是昼夜斑马鱼和夜间小鼠睡眠的关键后脑结构。使用遗传标记和钙成像,我们表明表达神经元支配并能激活 5-羟色胺能 RN 神经元。我们还证明,表达神经元的化学遗传学或光遗传学刺激以需要 RN 中的 NPVF 和 5-羟色胺的方式诱导睡眠。最后,我们提供了遗传证据,表明 NPVF 在 RN 中作为 5-羟色胺的上游物质发挥作用,以维持正常的睡眠水平。这些发现揭示了一个新的下丘脑-后脑神经元睡眠/觉醒控制回路。