MKP-1 antagonizes C/EBPβ activity and lowers the apoptotic threshold after ischemic injury

Cell Death Differ. 2012 Oct;19(10):1634-43. doi: 10.1038/cdd.2012.41. Epub 2012 Apr 20.

Abstract

The dual specificity phosphatase MAPK phosphatase-1 (MKP-1) feeds back on MAP kinase signaling to regulate metabolic, inflammatory and survival responses. MKP-1 is widely expressed in the central nervous system (CNS) and induced after ischemic stress, although its function in these contexts remains unclear. Here we report that MKP-1 activated several cell death factors, including BCL2 and adenovirus E1B 19 kDa interacting protein 3, and caspases 3 and 12 culminating in apoptotic cell death in vitro. MKP-1 also exerted inhibitory effects on the bZIP transcription factor CCAAT/enhancer-binding protein (C/EBPβ), previously shown to have neuroprotective properties. These effects included reduced expression of the full-length C/EBPβ variant and hypo-phosphorylation at the MEK-ERK1/2-sensitive Thr(188) site. Notably, enforced expression C/EBPβ rescued cells from MKP-1-induced toxicity. Studies performed in knock-out mice indicate that the MKP-1 activity is required to exclude C/EBPβ from the nucleus basally, and that MKP-1 antagonizes C/EBPβ expression after global forebrain ischemia, particularly within the vulnerable CA1 sector of the hippocampus. Overall, MKP-1 appears to lower the cellular apoptotic threshold by inhibiting C/EBPβ and enhancing both BH3 protein expression and cellular caspase activity. Thus, although manipulation of the MKP-1-C/EBPβ axis could have therapeutic value in ischemic disorders, our observations using MKP-1 catalytic mutants suggest that approaches geared towards inhibiting MKP-1's phosphatase activity alone may be ineffective.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis
  • CCAAT-Enhancer-Binding Protein-beta / antagonists & inhibitors
  • CCAAT-Enhancer-Binding Protein-beta / metabolism*
  • Caspase 12 / metabolism
  • Caspase 3 / metabolism
  • Cell Hypoxia
  • Cell Line
  • Dual Specificity Phosphatase 1 / deficiency
  • Dual Specificity Phosphatase 1 / genetics
  • Dual Specificity Phosphatase 1 / metabolism*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mitochondrial Proteins / metabolism
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Phosphorylation
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Transcriptional Activation

Substances

  • BNip3 protein, mouse
  • CCAAT-Enhancer-Binding Protein-beta
  • Membrane Proteins
  • Mitochondrial Proteins
  • Pmaip1 protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Dual Specificity Phosphatase 1
  • Dusp1 protein, mouse
  • Caspase 12
  • Caspase 3