Neutral lipid processing in glia is sexually dimorphic and promotes sleep through diacylglycerol catabolism
Year: 2025
Type: preprint
Abstract: Sleep is thought to have a protective role in clearing toxic waste from the brain, which may include processing of damaged lipids. We recently showed that blocking endocytosis in glia increases sleep and report here that this block is associated with an increase in peroxidized lipids and glial lipid droplet accumulation, raising the possibility that accumulation of these lipids increases the need to sleep. Sleep gain induced by blocking glial transport is exaggerated by knockout of the lipid droplet coat protein, Lipid Storage Droplet 2 ( Lsd2 ), suggesting that sleep-promoting lipids are not contained in lipid droplets. To identify lipids regulated by sleep state, we performed global, targeted lipidomics analysis on Drosophila neurons and glia, screening nearly 3,000 lipids across 11 major classes. This revealed that sex influences lipid composition in both cell types and lipid homeostasis following extended wakefulness. Female neurons and glia are enriched in ultra-long chain fatty acids, triacylglycerols, and diacylglycerols, with glial diacylglycerol enrichment correlating with elevated sleep need. Based on manipulations of neutral lipid metabolic pathways, we propose that monoacylglycerols, products of glial diacylglycerol catabolism, promote sleep.
Authors: Elana S. Pyfrom, Connor Beveridge, Paula R. Haynes, Vishal A. Kanigicherla, Caitlin E. Randolph, Paula Carvalho Costa, Seble G. Negatu, Sanjay Iyer, Samantha L. Killiany, Zhifeng Yue, Erick N. Astacio, Katherine A. Walker, Kiet N. Luu, Pavel A. Pivarshev, Kellie A. Jurado, Gaurav Chopra, Amita Sehgal
Language: English
Subfield: Biochemistry
Domain: Life Sciences
Open Access status: green
Award: G6943416789
OpenAlex ID: W4414260812
