A neuron-glia lipid metabolic cycle couples daily sleep to mitochondrial homeostasis.
Paula R HaynesElana S PyfromYongjun LiCarly SteinVishnu Anand CuddapahJack A JacobsZhifeng YueAmita SehgalPublished in: Nature neuroscience (2024)
Sleep is thought to be restorative to brain energy homeostasis, but it is not clear how this is achieved. We show here that Drosophila glia exhibit a daily cycle of glial mitochondrial oxidation and lipid accumulation that is dependent on prior wake and requires the Drosophila APOE orthologs NLaz and GLaz, which mediate neuron-glia lipid transfer. In turn, a full night of sleep is required for glial lipid clearance, mitochondrial oxidative recovery and maximal neuronal mitophagy. Knockdown of neuronal NLaz causes oxidative stress to accumulate in neurons, and the neuronal mitochondrial integrity protein, Drp1, is required for daily glial lipid accumulation. These data suggest that neurons avoid accumulation of oxidative mitochondrial damage during wake by using mitophagy and passing damage to glia in the form of lipids. We propose that a mitochondrial lipid metabolic cycle between neurons and glia reflects a fundamental function of sleep relevant for brain energy homeostasis.
Keyphrases
- oxidative stress
- physical activity
- sleep quality
- fatty acid
- spinal cord
- dna damage
- diabetic rats
- cerebral ischemia
- ischemia reperfusion injury
- induced apoptosis
- type diabetes
- resting state
- white matter
- depressive symptoms
- multiple sclerosis
- skeletal muscle
- metabolic syndrome
- deep learning
- functional connectivity
- hydrogen peroxide
- subarachnoid hemorrhage
- electronic health record
- blood brain barrier
- fluorescent probe
- data analysis