Peking-Tsinghua Center for Life Sciences, State Key Laboratory of Biomembrane and Membrane Biology, PKU-IDG/McGovern Institute For Brain Research, Beijing Advanced Innovation Center for Genomics, School of Life Sciences, Peking University, Beijing, China.
National Institute of Biological Sciences, Beijing, China.
Elife. 2017 Oct 6;6:e26519. doi: 10.7554/eLife.26519.
Our understanding of the molecular mechanisms underlying sleep homeostasis is limited. We have taken a systematic approach to study neural signaling by the transmitter 5-hydroxytryptamine (5-HT) in drosophila. We have generated knockout and knockin lines for , the 5-HT synthesizing enzyme and all five 5-HT receptors, making it possible for us to determine their expression patterns and to investigate their functional roles. Loss of the , or gene decreased sleep time whereas loss of the or gene diminished sleep rebound after sleep deprivation. expression in a small subset of, probably a single pair of, neurons in the dorsal fan-shaped body (dFB) is functionally essential: elimination of the gene from these neurons led to loss of sleep homeostasis. Genetic ablation of 5HT2b neurons in the dFB decreased sleep and impaired sleep homeostasis. Our results have shown that serotonergic signaling in specific neurons is required for the regulation of sleep homeostasis.
我们对睡眠稳态的分子机制的理解是有限的。我们采取了系统的方法来研究果蝇中递质 5-羟色胺(5-HT)的神经信号。我们生成了用于 5-HT 合成酶和所有五种 5-HT 受体的基因敲除和基因敲入系,这使我们能够确定它们的表达模式并研究它们的功能作用。失去 、 或 基因会减少睡眠时间,而失去 或 基因会减少睡眠剥夺后的睡眠反弹。在背扇形体(dFB)中的一小部分神经元中表达 ,可能是一对神经元,在功能上是必需的:从这些神经元中消除 基因导致睡眠稳态丧失。dFB 中的 5-HT2b 神经元的遗传消融会减少睡眠并损害睡眠稳态。我们的结果表明,特定神经元中的 5-羟色胺能信号对于调节睡眠稳态是必需的。