| Literature DB >> 30174114 |
Anela Vukoja1, Ulises Rey2, Astrid G Petzoldt3, Christoph Ott1, Dennis Vollweiter1, Christine Quentin3, Dymtro Puchkov1, Eric Reynolds3, Martin Lehmann1, Svea Hohensee1, Stefanie Rosa4, Reinhard Lipowsky5, Stephan J Sigrist6, Volker Haucke7.
Abstract
Nervous system function relies on the polarized architecture of neurons, established by directional transport of pre- and postsynaptic cargoes. While delivery of postsynaptic components depends on the secretory pathway, the identity of the membrane compartment(s) supplying presynaptic active zone (AZ) and synaptic vesicle (SV) proteins is unclear. Live imaging in Drosophila larvae and mouse hippocampal neurons provides evidence that presynaptic biogenesis depends on axonal co-transport of SV and AZ proteins in presynaptic lysosome-related vesicles (PLVs). Loss of the lysosomal kinesin adaptor Arl8 results in the accumulation of SV- and AZ-protein-containing vesicles in neuronal cell bodies and a corresponding depletion of SV and AZ components from presynaptic sites, leading to impaired neurotransmission. Conversely, presynaptic function is facilitated upon overexpression of Arl8. Our data reveal an unexpected function for a lysosome-related organelle as an important building block for presynaptic biogenesis.Entities:
Keywords: Drosophila; active zone; axonal transport; hippocampal neurons; lysosomes; neuromuscular junction; neurotransmission; synapse; synaptic vesicle; transport vesicle
Mesh:
Year: 2018 PMID: 30174114 DOI: 10.1016/j.neuron.2018.08.004
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173