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dc.rights.licenseopenen_US
dc.contributor.authorLI, Yingge
dc.contributor.authorZHOU, Xiaoya
dc.contributor.authorCHENG, Chen
dc.contributor.authorDING, Guangming
dc.contributor.authorZHAO, Peng
dc.contributor.authorTAN, Kai
dc.contributor.authorCHEN, Lixia
dc.contributor.authorPERRIMON, Norbert
hal.structure.identifierInstitut de Neurosciences cognitives et intégratives d'Aquitaine [INCIA]
dc.contributor.authorVEENSTRA, Jan-Adrianus
dc.contributor.authorZHANG, Luoying
dc.contributor.authorSONG, Wei
dc.date.accessioned2024-09-16T09:01:44Z
dc.date.available2024-09-16T09:01:44Z
dc.date.issued2023-05-23
dc.identifier.issn2056-5968en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/201590
dc.description.abstractEnSevere sleep deprivation (SD) has been highly associated with systemic energy wasting, such as lipid loss and glycogen depletion. Despite immune dysregulation and neurotoxicity observed in SD animals, whether and how the gut-secreted hormones participate in SD-induced disruption of energy homeostasis remains largely unknown. Using Drosophila as a conserved model organism, we characterize that production of intestinal Allatostatin A (AstA), a major gut-peptide hormone, is robustly increased in adult flies bearing severe SD. Interestingly, the removal of AstA production in the gut using specific drivers significantly improves lipid loss and glycogen depletion in SD flies without affecting sleep homeostasis. We reveal the molecular mechanisms whereby gut AstA promotes the release of an adipokinetic hormone (Akh), an insulin counter-regulatory hormone functionally equivalent to mammalian glucagon, to mobilize systemic energy reserves by remotely targeting its receptor AstA-R2 in Akh-producing cells. Similar regulation of glucagon secretion and energy wasting by AstA/galanin is also observed in SD mice. Further, integrating single-cell RNA sequencing and genetic validation, we uncover that severe SD results in ROS accumulation in the gut to augment AstA production via TrpA1. Altogether, our results demonstrate the essential roles of the gut-peptide hormone AstA in mediating SD-associated energy wasting.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enGut AstA mediates sleep deprivation-induced energy wasting in Drosophila
dc.title.alternativeCell Discoven_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41421-023-00541-3en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed37221172en_US
bordeaux.journalCell Discoveryen_US
bordeaux.volume9en_US
bordeaux.hal.laboratoriesInstitut de neurosciences cognitives et intégratives d'Aquitaine (INCIA) - UMR 5287en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
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hal.popularnonen_US
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dc.rights.ccCC BYen_US
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