Sleep pressure modulates single-neuron synapse number in zebrafish

• 成果类型: Article
• 署名作者: Suppermpool, Anya; Lyons, Declan G.; Broom, Elizabeth; Rihel, Jason
• 署名单位: University of London; University College London; University of London; University College London
• 刊物名称: Nature
• ISSN/ISSBN: 0028-5483
• DOI: 10.1038/s41586-024-07367-3
• 发表日期: 2024-05-16
• 关键词: visual-system; homeostasis; plasticity; potentiation; deprivation; wakefulness; melatonin; proteins; memory; wake

摘要

Sleep is a nearly universal behaviour with unclear functions 1 . The synaptic homeostasis hypothesis proposes that sleep is required to renormalize the increases in synaptic number and strength that occur during wakefulness 2 . Some studies examining either large neuronal populations 3 or small patches of dendrites 4 have found evidence consistent with the synaptic homeostasis hypothesis, but whether sleep merely functions as a permissive state or actively promotes synaptic downregulation at the scale of whole neurons is unclear. Here, by repeatedly imaging all excitatory synapses on single neurons across sleep-wake states of zebrafish larvae, we show that synapses are gained during periods of wake (either spontaneous or forced) and lost during sleep in a neuron-subtype-dependent manner. However, synapse loss is greatest during sleep associated with high sleep pressure after prolonged wakefulness, and lowest in the latter half of an undisrupted night. Conversely, sleep induced pharmacologically during periods of low sleep pressure is insufficient to trigger synapse loss unless adenosine levels are boosted while noradrenergic tone is inhibited. We conclude that sleep-dependent synapse loss is regulated by sleep pressure at the level of the single neuron and that not all sleep periods are equally capable of fulfilling the functions of synaptic homeostasis. Synapses are gained during spontaneous or forced periods of wake and lost during sleep in a neuron-subtype-dependent manner in zebrafish.