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  • 1
    In: Nature Communications, Springer Science and Business Media LLC, Vol. 14, No. 1 ( 2023-11-20)
    Abstract: Inflammation in the brain and gut is a critical component of several neurological diseases, such as Parkinson’s disease (PD). One trigger of the immune system in PD is aggregation of the pre-synaptic protein, α-synuclein (αSyn). Understanding the mechanism of propagation of αSyn aggregates is essential to developing disease-modifying therapeutics. Using a brain-first mouse model of PD, we demonstrate αSyn trafficking from the brain to the ileum of male mice. Immunohistochemistry revealed that the ileal αSyn aggregations are contained within CD11c + cells. Using single-cell RNA sequencing, we demonstrate that ileal CD11c + cells are microglia-like and the same subtype of cells is activated in the brain and ileum of PD mice. Moreover, by utilizing mice expressing the photo-convertible protein, Dendra2, we show that CD11c + cells traffic from the brain to the ileum. Together these data provide a mechanism of αSyn trafficking between the brain and gut.
    Type of Medium: Online Resource
    ISSN: 2041-1723
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2023
    detail.hit.zdb_id: 2553671-0
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  • 2
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 40, No. 50 ( 2020-12-09), p. 9617-9633
    Abstract: Dopamine is a wake-promoting neuromodulator in mammals and fruit flies. In Drosophila melanogaster , the network of clock neurons that drives sleep/activity cycles comprises both wake-promoting and sleep-promoting cell types. The large ventrolateral neurons (l-LN v s) and small ventrolateral neurons (s-LN v s) have been identified as wake-promoting neurons within the clock neuron network. The l-LN v s are innervated by dopaminergic neurons, and earlier work proposed that dopamine signaling raises cAMP levels in the l-LN v s and thus induces excitatory electrical activity (action potential firing), which results in wakefulness and inhibits sleep. Here, we test this hypothesis by combining cAMP imaging and patch-clamp recordings in isolated brains. We find that dopamine application indeed increases cAMP levels and depolarizes the l-LN v s, but, surprisingly, it does not result in increased firing rates. Downregulation of the excitatory D 1 -like dopamine receptor (Dop1R1) in the l-LN v s and s-LN v s, but not of Dop1R2, abolished the depolarization of l-LN v s in response to dopamine. This indicates that dopamine signals via Dop1R1 to the l-LN v s. Downregulation of Dop1R1 or Dop1R2 in the l-LN v s and s-LN v s does not affect sleep in males. Unexpectedly, we find a moderate decrease of daytime sleep with downregulation of Dop1R1 and of nighttime sleep with downregulation of Dop1R2. Since the l-LN v s do not use Dop1R2 receptors and the s-LN v s also respond to dopamine, we conclude that the s-LN v s are responsible for the observed decrease in nighttime sleep. In summary, dopamine signaling in the wake-promoting LN v s is not required for daytime arousal, but likely promotes nighttime sleep via the s-LN v s. SIGNIFICANCE STATEMENT In insect and mammalian brains, sleep-promoting networks are intimately linked to the circadian clock, and the mechanisms underlying sleep and circadian timekeeping are evolutionarily ancient and highly conserved. Here we show that dopamine, one important sleep modulator in flies and mammals, plays surprisingly complex roles in the regulation of sleep by clock-containing neurons. Dopamine inhibits neurons in a central brain sleep center to promote sleep and excites wake-promoting circadian clock neurons. It is therefore predicted to promote wakefulness through both of these networks. Nevertheless, our results reveal that dopamine acting on wake-promoting clock neurons promotes sleep, revealing a previously unappreciated complexity in the dopaminergic control of sleep.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2020
    detail.hit.zdb_id: 1475274-8
    SSG: 12
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