Neural reactivation during human sleep

Denis, Dan; Cairney, Scott

doi:10.31219/osf.io/zk92t

Cited by 1 publication

(1 citation statement)

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“…The relationship between sleep and memory is well documented (13, 50, 51). In particular, sleep plays a role in the consolidation of STM into LTM (52). Employing genetic and pharmacological activation, previous studies have demonstrated that inducing sleep after a courtship memory training protocol that is sufficient to create STM but not LTM, could convert that STM to LTM in Drosophila (14, 18, 19).…”

Section: Resultsmentioning

confidence: 99%

The dorsal fan-shaped body is a neurochemically heterogeneous sleep-regulating center inDrosophila

Jones,

Holder,

Montgomery

et al. 2024

Preprint

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Sleep is a behavior that is conserved throughout the animal kingdom. Yet, despite extensive studies in humans and animal models, the exact function or functions of sleep remain(s) unknown. A complicating factor in trying to elucidate the function of sleep is the complexity and multiplicity of neuronal circuits that are involved in sleep regulation. It is conceivable that distinct sleep-regulating circuits are only involved in specific aspects of sleep and may underlie different sleep functions. Thus, it would be beneficial to assess the contribution of individual circuits in sleep’s putative functions. The intricacy of the mammalian brain makes this task extremely difficult. However, the fruit flyDrosophila melanogaster,with its simpler brain organization, available connectomics, and unparalleled genetics offers the opportunity to interrogate individual sleep-regulating centers. InDrosophila, neurons projecting to the dorsal Fan-Shaped Body (dFB) have been proposed to be key regulators of sleep, particularly sleep homeostasis. We recently demonstrated that the most widely used genetic tool to manipulate dFB neurons, the 23E10-GAL4 driver, expresses in two sleep-regulating neurons (VNC-SP neurons) located in the Ventral Nerve Cord (VNC), the fly analog of the vertebrate spinal cord. Since most data supporting a role for the dFB in sleep regulation have been obtained using 23E10-GAL4, it is unclear whether the sleep phenotypes reported in these studies are caused by dFB neurons or VNC-SP cells. A recent publication replicated our finding that 23E10-GAL4 contains sleep-promoting neurons in the VNC. However, it also proposed that the dFB is not involved in sleep regulation at all. Unfortunately, this suggestion was made using genetic tools that are not dFB-specific. In this study, using a newly created dFB-specific genetic driver line, we demonstrate that the majority of 23E10-GAL4 dFB neurons can promote sleep when activated and that these neurons are involved in sleep homeostasis. In addition, we show that dFB neurons are neurochemically heterogeneous. Most dFB neurons express both glutamate and acetylcholine, while a minority of cells express only one of these two neurotransmitters. Importantly, dFB neurons do not express GABA, as previously suggested. Using neurotransmitter-specific dFB tools, our data also points at cholinergic dFB neurons as particularly potent at promoting sleep. Finally, we demonstrate that dFB-induced sleep can consolidate Short-Term Memory (STM) into Long-Term Memory (LTM), suggesting that the benefit of sleep on memory is not circuit-specific.

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