Phosphorylation and SUMOylation of CRMP2 regulate the formation and maturation of dendritic spines

Brain Res Bull. 2018 May:139:21-30. doi: 10.1016/j.brainresbull.2018.02.004. Epub 2018 Feb 6.

Abstract

The posttranslational modifications of CRMP2 play an important role in axon outgrowth, cell polarization and dendritic morphogenesis. However, whether CRMP2 and its posttranslational modifications are involved in dendritic spine development specifically is not completely clear. Here, we show that CRMP2 can promote the formation and maturation of dendritic spines in cultured hippocampal neurons. Overexpression of CRMP2 results in an increase in the density of spines especially the mushroom-shape spines. The amplitude and frequency of miniature excitatory postsynaptic currents (mEPSCs) are both enhanced and the intensity of PSD95 is strengthened in the neurons with CRMP2 overexpression. Furthermore, dephosphorylation of CRMP2 at Thr514 and deSUMOylation at Lys374 can further promote the formation and maturation of dendritic spines, whereas, no cross-talk is found between these two posttranslational modifications in the regulation of dendritic spine formation and maturation. Taken together, our data support a model in which phosphorylation and SUMOylation modification of CRMP2 independently promote the formation and maturation of dendritic spines and participate in the process of dendritic spine plasticity.

Keywords: CRMP2; Dendritic spine; Neuron; Phosphorylation; SUMOylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Dendritic Spines / physiology*
  • Disks Large Homolog 4 Protein / genetics
  • Disks Large Homolog 4 Protein / metabolism
  • Excitatory Postsynaptic Potentials / physiology
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hippocampus / cytology
  • Intercellular Signaling Peptides and Proteins
  • Luminescent Proteins / metabolism
  • Lysine / genetics
  • Lysine / metabolism
  • Male
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Neurons / cytology*
  • Phosphorylation / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Red Fluorescent Protein
  • SUMO-1 Protein / pharmacology
  • Sumoylation / physiology*
  • Threonine / metabolism

Substances

  • Disks Large Homolog 4 Protein
  • Dlg4 protein, rat
  • Intercellular Signaling Peptides and Proteins
  • Luminescent Proteins
  • Nerve Tissue Proteins
  • SUMO-1 Protein
  • SUMO1 protein, human
  • collapsin response mediator protein-2
  • Green Fluorescent Proteins
  • Threonine
  • Lysine