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Sleep homeostasis regulated by 5HT2b receptor in a small subset of neurons in the dorsal fan-shaped body of drosophila

机译:果蝇背扇形体中一小部分神经元的5HT2b受体调节睡眠稳态

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摘要

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 Trh, 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 Trh, 5HT1a or 5HT2b gene decreased sleep time whereas loss of the Trh or 5HT2b gene diminished sleep rebound after sleep deprivation. 5HT2b 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 5HT2b 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.
机译:我们对睡眠稳态的分子机制的理解是有限的。我们采用了系统的方法来研究果蝇中5-羟色胺(5-HT)的神经信号传递。我们已经生成了Trh,5-HT合成酶和所有五个5-HT受体的敲除和敲除系,这使我们能够确定它们的表达模式并研究其功能作用。 Trh,5HT1a或5HT2b基因的丢失减少了睡眠时间,而Trh或5HT2b基因的丢失则减少了睡眠剥夺后的睡眠反弹。 5HT2b在背扇形体(dFB)的一小部分神经元中表达可能是功能上必不可少的:从这些神经元中消除5HT2b基因会导致睡眠稳态的丧失。 dFB中5HT2b神经元的遗传消融可减少睡眠并损害睡眠稳态。我们的结果表明,特定神经元的血清素能信号传导是调节睡眠稳态所需的。

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