Single-cell transcriptomics reveals that glial cells integrate homeostatic and circadian processes to drive sleep-wake cycles.
Joana DoppAntonio OrtegaKristofer DavieSuresh PoovathingalEl-Sayed BazSha LiuPublished in: Nature neuroscience (2024)
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.
Keyphrases
- single cell
- sleep quality
- physical activity
- rna seq
- gene expression
- high throughput
- genome wide
- stem cells
- dna methylation
- transcription factor
- induced apoptosis
- signaling pathway
- spinal cord injury
- white matter
- mesenchymal stem cells
- young adults
- functional connectivity
- genome wide identification
- single molecule
- childhood cancer