FLIM FRET Visualization of Cdc42 Activation by Netrin-1 in Embryonic Spinal Commissural Neuron Growth Cones

PLoS One. 2016 Aug 2;11(8):e0159405. doi: 10.1371/journal.pone.0159405. eCollection 2016.

Abstract

Netrin-1 is an essential extracellular chemoattractant that signals through its receptor DCC to guide commissural axon extension in the embryonic spinal cord. DCC directs the organization of F-actin in growth cones by activating an intracellular protein complex that includes the Rho GTPase Cdc42, a critical regulator of cell polarity and directional migration. To address the spatial distribution of signaling events downstream of netrin-1, we expressed the FRET biosensor Raichu-Cdc42 in cultured embryonic rat spinal commissural neurons. Using FLIM-FRET imaging we detected rapid activation of Cdc42 in neuronal growth cones following application of netrin-1. Investigating the signaling mechanisms that control Cdc42 activation by netrin-1, we demonstrate that netrin-1 rapidly enriches DCC at the leading edge of commissural neuron growth cones and that netrin-1 induced activation of Cdc42 in the growth cone is blocked by inhibiting src family kinase signaling. These findings reveal the activation of Cdc42 in embryonic spinal commissural axon growth cones and support the conclusion that src family kinase activation downstream of DCC is required for Cdc42 activation by netrin-1.

MeSH terms

  • Animals
  • Cells, Cultured
  • DCC Receptor
  • Fluorescence Resonance Energy Transfer / methods*
  • Growth Cones / metabolism
  • Growth Cones / ultrastructure*
  • Microdissection
  • Microscopy, Fluorescence / methods*
  • Nerve Growth Factors / analysis*
  • Nerve Growth Factors / metabolism
  • Netrin-1
  • Rats, Sprague-Dawley
  • Receptors, Cell Surface / analysis
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Spinal Cord / cytology
  • Spinal Cord / embryology*
  • Spinal Cord / metabolism
  • Spinal Cord / ultrastructure
  • Tumor Suppressor Proteins / analysis*
  • Tumor Suppressor Proteins / metabolism
  • cdc42 GTP-Binding Protein / analysis*
  • cdc42 GTP-Binding Protein / metabolism
  • src-Family Kinases / metabolism

Substances

  • DCC Receptor
  • Dcc protein, rat
  • Nerve Growth Factors
  • Ntn1 protein, rat
  • Receptors, Cell Surface
  • Tumor Suppressor Proteins
  • Netrin-1
  • src-Family Kinases
  • cdc42 GTP-Binding Protein

Grants and funding

This work was supported by operating grants from the Canadian Institutes of Health Research (114965, 126109: Kennedy), a CREATE training grant from the Natural Sciences and Engineering Research Council of Canada, and a Natural Sciences and Engineering Research Council of Canada Discovery Grant (250013-12 Wiseman). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.