Inhibition of EphA4 signaling after ischemia-reperfusion reduces apoptosis of CA1 pyramidal neurons

Neurosci Lett. 2012 Jun 19;518(2):92-5. doi: 10.1016/j.neulet.2012.04.060. Epub 2012 May 3.

Abstract

Hippocampal CA1 pyramidal neurons are sensitive to ischemic damage. However, the cellular and molecular mechanisms underlying neuronal cell death caused by ischemia-reperfusion (I/R) are not completely clear. Here, we report that the ephrinA/EphA cell-cell interaction signaling pathway plays an important role in the apoptosis of hippocampal CA1 pyramidal neurons induced by I/R. We found that the expression of ephrinA3 and EphA4 is increased in the CA1 region following transient forebrain ischemia. Blocking ephrinA3/EphA4 interaction by EphA4-Fc, an inhibitor of EphA4, attenuated apoptotic neuronal cell death, likely through the inhibition of caspase-3 activation. These results reveal a novel function of ephrin/Eph signaling in the regulation of apoptosis in CA1 pyramidal neurons after I/R.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Blotting, Western
  • Brain Ischemia / metabolism*
  • CA1 Region, Hippocampal / metabolism
  • In Situ Nick-End Labeling
  • Male
  • Pyramidal Cells / metabolism*
  • Rats
  • Rats, Wistar
  • Receptor, EphA4 / metabolism*
  • Reperfusion Injury / metabolism*
  • Signal Transduction / physiology*

Substances

  • Receptor, EphA4