Modulation of sleep by trafficking of lipids through the Drosophila blood-brain barrier

Abstract

Endocytosis through <i>Drosophila</i> glia is a significant determinant of sleep amount and occurs preferentially during sleep in glia of the blood-brain barrier (BBB). To identify metabolites whose trafficking is mediated by sleep-dependent endocytosis, we conducted metabolomic analysis of flies that have increased sleep due to a block in glial endocytosis. We report that acylcarnitines, fatty acids conjugated to carnitine to promote their transport, accumulate in heads of these animals. In parallel, to identify transporters and receptors whose loss contributes to the sleep phenotype caused by blocked endocytosis, we screened genes enriched in barrier glia for effects on sleep. We find that knockdown of lipid transporters <i>LRP1</i>&2 or of carnitine transporters <i>ORCT1</i>&2 increases sleep. In support of the idea that the block in endocytosis affects trafficking through specific transporters, knockdown of <i>LRP</i> or <i>ORCT</i> transporters also increases acylcarnitines in heads. We propose that lipid species, such as acylcarnitines, are trafficked through the BBB via sleep-dependent endocytosis, and their accumulation reflects an increased need for sleep.