Temporal profiles of high-mobility group box 1 expression levels after cortical spreading depression in mice

Cephalalgia. 2016 Jan;36(1):44-52. doi: 10.1177/0333102415580100. Epub 2015 Apr 10.

Abstract

Introduction: Cortical spreading depression (CSD) has recently been shown to induce the release of the nuclear protein termed high-mobility group box 1 from neurons, causing activation of the trigeminovascular system. Here, we explored the effects of single and multiple cortical spreading depression inductions on high-mobility group box 1 (HMGB1) transcriptional activity relative to high-mobility group box 1 protein expression levels and intracellular localization in cortical neurons and astrocytes.

Methods: Single or multiple cortical spreading depression inductions were achieved by KCl application to the mouse cerebral cortex. The animals were sacrificed at 30 minutes, 3 hours and 24 hours after cortical spreading depression induction. High-mobility group box 1 expression levels were explored with in situ hybridization, Western blotting and immunostaining.

Results: Cortical spreading depression up-regulated high-mobility group box 1 transcriptional activity in neurons at 3 hours in a manner that was dependent on the number of cortical spreading depression inductions. At 24 hours, the high-mobility group box 1 transcriptional activity had returned to basal levels. Cortical spreading depression induced a reduction in high-mobility group box 1 protein expression at 3 hours, which was also dependent on the number of cortical spreading depression inductions. Following cortical spreading depression, the release of high-mobility group box 1 from the nucleus was observed in a small proportion of neurons, but not in astrocytes.

Conclusion: Cortical spreading depression induced translocation of high-mobility group box 1 from neuronal nuclei, driving transcriptional up-regulation of high-mobility group box 1 to maintain protein levels.

Keywords: Cortical spreading depression; astrocyte; high-mobility group box 1; neuron; transcriptional activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Cortical Spreading Depression / physiology*
  • Gene Expression Regulation
  • HMGB1 Protein / biosynthesis*
  • HMGB1 Protein / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Parietal Lobe / metabolism*
  • Time Factors

Substances

  • HMGB1 Protein
  • HMGB1 protein, mouse