Center for Brain & Disease Research, VIB-KU Leuven, Leuven, Belgium.
Department of Neurosciences, KU Leuven, Leuven, Belgium.
Nat Neurosci. 2024 Feb;27(2):359-372. doi: 10.1038/s41593-023-01549-4. Epub 2024 Jan 23.
The sleep-wake cycle is determined by circadian and sleep homeostatic processes. However, the molecular impact of these processes and their interaction in different brain cell populations are unknown. To fill this gap, we profiled the single-cell transcriptome of adult Drosophila brains across the sleep-wake cycle and four circadian times. We show cell type-specific transcriptomic changes, with glia displaying the largest variation. Glia are also among the few cell types whose gene expression correlates with both sleep homeostat and circadian clock. The sleep-wake cycle and sleep drive level affect the expression of clock gene regulators in glia, and disrupting clock genes specifically in glia impairs homeostatic sleep rebound after sleep deprivation. These findings provide a comprehensive view of the effects of sleep homeostatic and circadian processes on distinct cell types in an entire animal brain and reveal glia as an interaction site of these two processes to determine sleep-wake dynamics.
睡眠-觉醒周期由昼夜节律和睡眠内稳态过程决定。然而,这些过程的分子影响及其在不同脑细胞群体中的相互作用尚不清楚。为了填补这一空白,我们对成年果蝇大脑在睡眠-觉醒周期和四个昼夜时间点的单细胞转录组进行了分析。我们显示了细胞类型特异性转录组变化,其中神经胶质细胞的变化最大。神经胶质细胞也是少数与睡眠内稳态和生物钟都相关的基因表达的细胞类型之一。睡眠-觉醒周期和睡眠驱动力水平会影响神经胶质细胞中时钟基因调控因子的表达,而特异性地破坏神经胶质细胞中的时钟基因会损害睡眠剥夺后睡眠内稳态反弹。这些发现提供了一个全面的视角,展示了睡眠内稳态和昼夜节律过程对整个动物大脑中不同细胞类型的影响,并揭示了神经胶质细胞作为这两个过程相互作用的一个交互点,以决定睡眠-觉醒动力学。