Astrocytes are neuroglia cells in the central nervous system (CNS) with many functions, including metabolic homeostasis in the CNS and delivering nutrients (lactate, glucose) to neurons. During CNS pathologies, astrocytes accumulate lipid droplets (LDs), which serve as stores of free fatty acids (FA) and sterols. The mechanisms of LDs formation and their role in astrocytes are still poorly understood, as well as lipid signalling via G-protein coupled receptors for free FA (e.g., GPR40) on the surface of astrocytes and its effect on astrocyte metabolism. Using immunocytochemistry and confocal microscopy, we characterized subcellular localization, LD mobility and the effect of metabolic stress and hypoxia (typical stressors in CNS pathologies) and stress-related noradrenergic activation on LD formation in isolated and organotypic brain tissue astrocytes. Using real-time fluorescence microscopy we evaluated the effect of GPR40 agonists, endogenous non-selective agonist docosahexaenoic acid (DHA) and oleic acid (OA), and synthetic selective agonist TAK875, on intracellular Ca2+, cAMP and lactate concentration in astrocytes labelled with Ca2+-indicator (Fluo-4, AM) and genetically encoded FRET-based nanosensors for cAMP (Epac1-camps), PKA nanosensor (AKAR2) or lactate (Laconic). We found that LD mobility in astrocytes is, compared to other organelles, low and spatially limited, in close proximity to mitochondria and endoplasmic reticulum. Metabolic stress, hypoxia and noradrenergic activation triggers LD accumulation in astrocytes. Astroglial LD can serve in astrocytes as an alternative energy source (β-oxidation of free FA), but at the same time they protect CNS cells from lipototoxicity. We found that astrocytes express GPR40 and that stimulation with agonists of GPR40 (DHA, OA or TAK875) causes transient Ca2+ and persistent cAMP and lactate increases in astrocytes, suggesting that extracellular free FA can function as a signalling molecules regulating aerobic glycolysis and lactate production in astrocytes, which is an important source of energy to neurons.
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