This review synthesizes how LC3 versus GABARAP mediate distinct steps of autophagy (LC3 primarily governs cargo recruitment and phagophore expansion, whereas GABARAP drives autophagosome maturation, transport, and lysosomal fusion).
First-pass extracted concept
LC3-GABARAP specialization
Aliases
LC3 versus GABARAP specialization
Evidence Snippets
Supporting Sources
Linked Claims
Astrocytes use autophagy for metabolic support and clearance of extracellular debris such as amyloid-beta plaques, and interface with neuronal autophagy through transcellular mechanisms.
In neurons, presynaptic autophagy clears aging synaptic vesicles and organelles, while postsynaptic autophagy modulates receptor turnover and synaptic plasticity.
Dysregulated autophagic flux and aggregate clearance contribute to neurodegenerative diseases including Alzheimer's and Parkinson's disease, and selective synaptic autophagy deficits are implicated in epilepsy and autism.
An emerging ATG8 code assigns specialized autophagy roles to mammalian LC3 and GABARAP paralogs.
LC3 primarily governs cargo recruitment and phagophore expansion, whereas GABARAP drives autophagosome maturation, transport, and lysosomal fusion.