Golgi-resident TRIO regulates membrane trafficking during neurite outgrowth

J Biol Chem. 2019 Jul 12;294(28):10954-10968. doi: 10.1074/jbc.RA118.007318. Epub 2019 May 31.

Abstract

Neurite outgrowth requires coordinated cytoskeletal rearrangements in the growth cone and directional membrane delivery from the neuronal soma. As an essential Rho guanine nucleotide exchange factor (GEF), TRIO is necessary for cytoskeletal dynamics during neurite outgrowth, but its participation in the membrane delivery is unclear. Using co-localization studies, live-cell imaging, and fluorescence recovery after photobleaching analysis, along with neurite outgrowth assay and various biochemical approaches, we here report that in mouse cerebellar granule neurons, TRIO protein pools at the Golgi and regulates membrane trafficking by controlling the directional maintenance of both RAB8 (member RAS oncogene family 8)- and RAB10-positive membrane vesicles. We found that the spectrin repeats in Golgi-resident TRIO confer RAB8 and RAB10 activation by interacting with and activating the RAB GEF RABIN8. Constitutively active RAB8 or RAB10 could partially restore the neurite outgrowth of TRIO-deficient cerebellar granule neurons, suggesting that TRIO-regulated membrane trafficking has an important functional role in neurite outgrowth. Our results also suggest cross-talk between Rho GEF and Rab GEF in controlling both cytoskeletal dynamics and membrane trafficking during neuronal development. They further highlight how protein pools localized to specific organelles regulate crucial cellular activities and functions. In conclusion, our findings indicate that TRIO regulates membrane trafficking during neurite outgrowth in coordination with its GEF-dependent function in controlling cytoskeletal dynamics via Rho GTPases.

Keywords: Rab; Rho (Rho GTPase); guanine nucleotide exchange factor (GEF); membrane trafficking; neurite outgrowth; neurodevelopment; signal transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement
  • Cerebellum / metabolism
  • Golgi Apparatus / enzymology
  • Golgi Apparatus / metabolism
  • Growth Cones / metabolism
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Guanine Nucleotide Exchange Factors / physiology
  • Humans
  • Membrane Transport Proteins / metabolism
  • Mice
  • Neurites / metabolism*
  • Neurites / physiology
  • Neuronal Outgrowth / physiology*
  • Neurons / metabolism
  • Phosphoproteins / metabolism*
  • Phosphoproteins / physiology
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Serine-Threonine Kinases / physiology
  • Protein Transport
  • Signal Transduction / physiology
  • rab GTP-Binding Proteins / metabolism
  • rho GTP-Binding Proteins / metabolism

Substances

  • Guanine Nucleotide Exchange Factors
  • Membrane Transport Proteins
  • Phosphoproteins
  • Rab8 protein, mouse
  • Trio protein, mouse
  • Protein Serine-Threonine Kinases
  • Rab10 protein, mouse
  • rab GTP-Binding Proteins
  • rho GTP-Binding Proteins