Dendritic spine alterations in neocortical pyramidal neurons following postnatal neuronal Nogo-A knockdown

Dev Neurosci. 2010;32(4):313-20. doi: 10.1159/000309135. Epub 2010 Oct 13.

Abstract

The myelin-associated protein Nogo-A is a well-known inhibitor of axonal regeneration and compensatory plasticity, yet functions of neuronal Nogo-A are not as clear. The present study examined the effects of decreased levels of neuronal Nogo-A on dendritic spines of developing neocortical neurons. Decreased Nogo-A levels in these neurons resulted in lowered spine density and an increase in filopodial type protrusions. These results suggest a role for neuronal Nogo-A in maintaining a spine phenotype in neocortical pyramidal cells.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Dendritic Spines / metabolism
  • Dendritic Spines / ultrastructure*
  • Gene Knockdown Techniques
  • Humans
  • Image Processing, Computer-Assisted
  • Male
  • Microscopy, Confocal
  • Myelin Proteins / genetics
  • Myelin Proteins / metabolism*
  • Neocortex / metabolism
  • Neocortex / pathology*
  • Nogo Proteins
  • Pyramidal Cells / metabolism
  • Pyramidal Cells / ultrastructure*
  • RNA Interference
  • Rats

Substances

  • Myelin Proteins
  • Nogo Proteins
  • RTN4 protein, human
  • Rtn4 protein, rat