Enhanced SUMOylation and SENP-1 protein levels following oxygen and glucose deprivation in neurones

J Cereb Blood Flow Metab. 2012 Jan;32(1):17-22. doi: 10.1038/jcbfm.2011.146. Epub 2011 Oct 12.

Abstract

Here, we show that oxygen and glucose deprivation (OGD) causes increased small ubiquitin-like modifier (SUMO)-1 and SUMO-2/3 conjugation to substrate proteins in cultured hippocampal neurones. Surprisingly, the SUMO protease SENP-1, which removes SUMO from conjugated proteins, was also increased by OGD, suggesting that the neuronal response to OGD involves a complex interplay between SUMOylation and deSUMOylation. Importantly, decreasing global SUMOylation in cultured hippocampal neurones by overexpression of the catalytic domain of SENP-1 increased neuronal vulnerability to OGD-induced cell death. Taken together, these results suggest a neuroprotective role for neuronal SUMOylation after OGD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catalytic Domain
  • Cell Death
  • Cells, Cultured
  • Cloning, Molecular
  • Cysteine Endopeptidases
  • Endopeptidases / genetics
  • Endopeptidases / metabolism*
  • Glucose / metabolism*
  • Green Fluorescent Proteins / metabolism
  • Hippocampus / metabolism
  • Hippocampus / pathology
  • Mutation
  • Neurons / metabolism*
  • Neurons / pathology
  • Oxygen / metabolism*
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • SUMO-1 Protein / genetics
  • SUMO-1 Protein / metabolism*
  • Sindbis Virus / genetics
  • Sumoylation*

Substances

  • SUMO-1 Protein
  • Green Fluorescent Proteins
  • Endopeptidases
  • Cysteine Endopeptidases
  • SENP1 protein, rat
  • Glucose
  • Oxygen