PLoS ONE (Jan 2014)

Protein synthesis dependence of growth cone collapse induced by different Nogo-A-domains.

  • Richard Manns,
  • Andre Schmandke,
  • Antonio Schmandke,
  • Prem Jareonsettasin,
  • Geoffrey Cook,
  • Martin E Schwab,
  • Christine Holt,
  • Roger Keynes

DOI
https://doi.org/10.1371/journal.pone.0086820
Journal volume & issue
Vol. 9, no. 1
p. e86820

Abstract

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The protein Nogo-A regulates axon growth in the developing and mature nervous system, and this is carried out by two distinct domains in the protein, Nogo-A-Δ20 and Nogo-66. The differences in the signalling pathways engaged in axon growth cones by these domains are not well characterized, and have been investigated in this study.We analyzed growth cone collapse induced by the Nogo-A domains Nogo-A-Δ20 and Nogo-66 using explanted chick dorsal root ganglion neurons growing on laminin/poly-lysine substratum. Collapse induced by purified Nogo-A-Δ20 peptide is dependent on protein synthesis whereas that induced by Nogo-66 peptide is not. Nogo-A-Δ20-induced collapse is accompanied by a protein synthesis-dependent rise in RhoA expression in the growth cone, but is unaffected by proteasomal catalytic site inhibition. Conversely Nogo-66-induced collapse is inhibited ∼ 50% by proteasomal catalytic site inhibition.Growth cone collapse induced by the Nogo-A domains Nogo-A-Δ20 and Nogo-66 is mediated by signalling pathways with distinguishable characteristics concerning their dependence on protein synthesis and proteasomal function.