Sleep regulates the glial engulfment receptor Draper to promote Wallerian degeneration
Stahl, B. A.; Jaggard, J. B.; Keene, A. C.
Show abstract
Sleep, a universal behavior, is critical for diverse aspects of brain function. Chronic sleep disturbance is associated with numerous health consequences, including neurodegenerative disease and cognitive decline. Neurite damage due to apoptosis, trauma, or genetic factors is a common feature of aging, and clearance of damaged neurons is essential for maintenance of brain function. In the central nervous system, damaged neurites are cleared by Wallerian degeneration, in which activated microglia and macrophages engulf damaged neurons. The fruit fly Drosophila melanogaster provides a powerful model for investigating the relationship between sleep and Wallerian degeneration. Several lines of evidence suggest that glia influence sleep duration, sleep-mediated neuronal homeostasis, and clearance of toxic substances during sleep, raising the possibility that glial engulfment of damaged axons is regulated by sleep. To explore this possibility, we axotomized olfactory receptor neurons and measured the effects of sleep loss or gain on the clearance of damaged neurites. Mechanical sleep deprivation impaired the clearance of damaged neurites, whereas the sleep-promoting drug gaboxadol accelerated clearance. In sleep-deprived animals, multiple markers of glial activation were delayed, including activation of the JAK/STAT pathway, upregulation of the cell corpse engulfment receptor Draper, and innervation of the antennal lobe by glial membranes. These markers were all enhanced when sleep was induced in gaboxadol-treated flies. Taken together, these findings reveal a critical role for sleep in regulation glial activation and engulfment following axotomy, providing a platform for further investigations of the molecular mechanisms underlying sleep-dependent modulation of glial function and neurite clearance.\n\nHighlightsO_LISleep deprivation impairs Wallerian degeneration in fruit flies.\nC_LIO_LIPharmacological induction of sleep accelerates Wallerian degeneration.\nC_LIO_LISleep promotes innervation surrounding damaged neurites by phagocytic glia.\nC_LIO_LISleep increases levels of the glial activation markers Draper and Stat92E.\nC_LI
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Early-life nutrition interacts with developmental genes to shape the brain and sleep behavior in Drosophila melanogaster 96%
- A conserved role for sleep in supporting spatial learning in Drosophila 93%
- Immunization with Mycobacterium vaccae NCTC 11659 prevents the development of PTSD- like sleep and behavioral phenotypes after sleep disruption and acute stress in mice 92%
Similar papers in this journal
- The Drosophila Amyloid Precursor Protein homologue mediates neuronal survival and neuro-glial interactions 94%
- FBXO7/ntc and USP30 antagonistically set the ubiquitination threshold for basal mitophagy and provides a target for Pink1 phosphorylation in vivo 92%
- Upstream open reading frames dynamically modulate CLOCK protein translation to regulate circadian rhythm and sleep 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.