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
- spinal cord
- diabetic rats
- dna damage
- fatty acid
- cerebral ischemia
- ischemia reperfusion injury
- induced apoptosis
- white matter
- neuropathic pain
- resting state
- insulin resistance
- adipose tissue
- electronic health record
- nitric oxide
- functional connectivity
- resistance training
- artificial intelligence
- depressive symptoms
- body composition
- nlrp inflammasome
- multiple sclerosis
- signaling pathway
- brain injury
- subarachnoid hemorrhage
- fluorescent probe
- spinal cord injury
- data analysis