Unc-51-like kinase 1/2-mediated endocytic processes regulate filopodia extension and branching of sensory axons

Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):5842-7. doi: 10.1073/pnas.0701402104. Epub 2007 Mar 26.

Abstract

The molecular mechanism and significance of endocytic processes involved in directional axon elongation are not well understood. The Unc-51 family of serine/threonine kinases was shown to be important for axon growth and was also linked to endocytosis, providing an entry point to study this problem. We found that mouse Unc-51-like kinase 1/2 (Ulk1/2) proteins are localized to vesicular structures in growth cones of mouse spinal sensory neurons. RNAi-mediated knockdown of Ulk1 and/or Ulk2 resulted in impaired endocytosis of nerve growth factor (NGF), excessive axon arborization, and severely stunted axon elongation. The evidence also indicates that Ulk1/2 mediates a non-clathrin-coated endocytosis in sensory growth cones. Interestingly, NGF can induce the interaction of Ulk1 with TrkA receptor complexes through promoting K63-polyubiquitination of Ulk1 and binding of Ulk1 to the scaffolding protein p62. These results and additional studies suggest that Ulk1/2 proteins regulate filopodia extension and neurite branching during sensory axon outgrowth, probably through regulating TrkA receptor trafficking and signaling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy-Related Protein-1 Homolog
  • Axons / drug effects
  • Axons / physiology*
  • Cell Line
  • Embryo, Mammalian
  • Endocytosis*
  • Fluorescent Antibody Technique, Direct
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / enzymology
  • Green Fluorescent Proteins / metabolism
  • Growth Cones / enzymology
  • Growth Cones / physiology
  • Humans
  • Mice
  • Nerve Growth Factor / pharmacology
  • Neurites / physiology
  • Neurons, Afferent / enzymology
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Pseudopodia / physiology*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Receptor Cross-Talk / drug effects
  • Receptor, trkA / metabolism
  • Transcription Factor TFIIH
  • Transcription Factors / metabolism
  • Ubiquitin / metabolism

Substances

  • Gtf2h1 protein, mouse
  • RNA, Small Interfering
  • Transcription Factors
  • Ubiquitin
  • Green Fluorescent Proteins
  • Transcription Factor TFIIH
  • Nerve Growth Factor
  • Ulk2 protein, mouse
  • Receptor, trkA
  • Autophagy-Related Protein-1 Homolog
  • Protein Serine-Threonine Kinases
  • Ulk1 protein, mouse