Rab2 drives axonal transport of dense core vesicles and lysosomal organelles

Cell Rep. 2021 Apr 13;35(2):108973. doi: 10.1016/j.celrep.2021.108973.

Abstract

Fast axonal transport of neuropeptide-containing dense core vesicles (DCVs), endolysosomal organelles, and presynaptic components is critical for maintaining neuronal functionality. How the transport of DCVs is orchestrated remains an important unresolved question. The small GTPase Rab2 mediates DCV biogenesis and endosome-lysosome fusion. Here, we use Drosophila to demonstrate that Rab2 also plays a critical role in bidirectional axonal transport of DCVs, endosomes, and lysosomal organelles, most likely by controlling molecular motors. We further show that the lysosomal motility factor Arl8 is required as well for axonal transport of DCVs, but unlike Rab2, it is also critical for DCV exit from cell bodies into axons. We also provide evidence that the upstream regulators of Rab2 and Arl8, Ema and BORC, activate these GTPases during DCV transport. Our results uncover the mechanisms underlying axonal transport of DCVs and reveal surprising parallels between the regulation of DCV and lysosomal motility.

Keywords: Arl8; Drosophila; Rab2; axonal transport; dense core vesicles; endosomes; lysosomes; membrane trafficking; neuropeptides; synaptogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-Ribosylation Factors / genetics*
  • ADP-Ribosylation Factors / metabolism
  • Animals
  • Axonal Transport / genetics*
  • Dense Core Vesicles / metabolism*
  • Dense Core Vesicles / ultrastructure
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / metabolism
  • Endosomes / metabolism
  • Endosomes / ultrastructure
  • Gene Expression Regulation
  • Lectins, C-Type / genetics
  • Lectins, C-Type / metabolism
  • Lysosomes / metabolism
  • Lysosomes / ultrastructure
  • Membrane Fusion
  • Monosaccharide Transport Proteins / genetics
  • Monosaccharide Transport Proteins / metabolism
  • Multiprotein Complexes / genetics
  • Multiprotein Complexes / metabolism
  • Neurons / metabolism*
  • Neurons / ultrastructure
  • Organelle Biogenesis
  • Protein Binding
  • Signal Transduction
  • rab2 GTP-Binding Protein / genetics*
  • rab2 GTP-Binding Protein / metabolism

Substances

  • Arl8 protein, Drosophila
  • Drosophila Proteins
  • Ema protein, Drosophila
  • Lectins, C-Type
  • Monosaccharide Transport Proteins
  • Multiprotein Complexes
  • ADP-Ribosylation Factors
  • rab2 GTP-Binding Protein