Role of ERK map kinase and CRM1 in IL-1beta-stimulated release of HMGB1 from cortical astrocytes

Glia. 2010 Jun;58(8):1007-15. doi: 10.1002/glia.20982.

Abstract

Reactive astrocytes are traditionally thought to impede brain plasticity after stroke. However, we previously showed that reactive astrocytes may also contribute to stroke recovery, partly via the release of a nuclear protein called high-mobility group box 1 (HMGB1). Here, we investigate the mechanisms that allow stimulated astrocytes to release HMGB1. Exposure of rat primary astrocytes to IL-1beta for 24 h elicited a dose-dependent HMGB1 response. Immunostaining and western blots of cell lysates showed increased intracellular levels of HMGB1. Western blots confirmed that IL-1beta induced a release of HMGB1 into astrocyte conditioned media. MAP kinase signaling was involved. Levels of phospho-ERK were increased by IL-1beta, and the MEK/ERK inhibitor U0126 decreased HMGB1 upregulation in the stimulated astrocytes. Since HMGB1 is a nuclear protein, the role of the nuclear protein exporter, chromosome region maintenance 1 (CRM1), was assessed as a candidate mechanism for linking MAP kinase signaling to HMGB1 release. IL-1beta increased CRM1 expression in concert with a translocation of HMGB1 from nucleus into cytoplasm. Blockade of IL-1beta-stimulated HMGB1 release with the ERK inhibitor U0126 was accompanied by a downregulation of CRM1. Our findings reveal that IL-1beta stimulates the release of HMGB1 from activated astrocytes via ERK MAP kinase and CRM1 signaling. These data suggest a novel pathway by which inflammatory cytokines may enhance the ability of reactive astrocytes to release prorecovery mediators after stroke.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Astrocytes / drug effects*
  • Astrocytes / metabolism
  • Butadienes / pharmacology
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cerebral Cortex / cytology*
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Exportin 1 Protein
  • Fatty Acids, Unsaturated / pharmacology
  • HMGB1 Protein / metabolism*
  • Interleukin-1beta / pharmacology*
  • Karyopherins / metabolism*
  • Mitogen-Activated Protein Kinase Kinases / metabolism*
  • Nitriles / pharmacology
  • Protein Transport / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Signal Transduction / drug effects
  • Up-Regulation / drug effects

Substances

  • Butadienes
  • Enzyme Inhibitors
  • Fatty Acids, Unsaturated
  • HMGB1 Protein
  • Hbp1 protein, rat
  • Interleukin-1beta
  • Karyopherins
  • Nitriles
  • Receptors, Cytoplasmic and Nuclear
  • U 0126
  • Mitogen-Activated Protein Kinase Kinases
  • leptomycin B