Induction of phosphorylated-Stat3 following focal cerebral ischemia in mice

Neurosci Lett. 2001 May 11;303(3):153-6. doi: 10.1016/s0304-3940(01)01711-6.

Abstract

It has been shown that Stat3 is induced following transient cerebral ischemia in rat. However there is no evidence that cerebral ischemia stimulates the expression of phosphorylated-Stat3 (p-Stat3), which can activate cytokine-mediated signal transduction from the membrane to the nucleus. In the present study, we investigated the changes in p-Stat3 expression following middle cerebral artery occlusion in mice. Western blot analysis revealed a significant increase in the p-Stat3 protein in the peripheral part of the ischemic area, starting from 6 h after ischemia. p-Stat3 immunoreactivity was detected only in neurons, but not in astrocytes or microglia, and p-Stat3-positive neurons were increased in number in the peripheral part of the ischemic area at 24 h after ischemia. Double staining with aTdT-mediated biotinylated UTP nick end labeling (TUNEL) kit and the p-Stat3 antibody indicated that p-Stat3-positive neurons were also TUNEL-positive. Subsequent immuno-electron microscopic observations showed that p-Stat3-positive neurons were at different stages of degeneration. The present findings suggest that the increased expression of p-Stat3 after cerebral ischemia could play a crucial role in ischemia-induced neuron death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Ischemia / metabolism*
  • Brain Ischemia / pathology
  • Brain Ischemia / physiopathology
  • Cell Death / physiology
  • Cell Membrane / metabolism
  • Cell Membrane / pathology
  • Cell Membrane / ultrastructure
  • Cytokines / metabolism
  • DNA-Binding Proteins / metabolism*
  • Disease Models, Animal
  • Gene Expression Regulation / physiology
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Infarction, Middle Cerebral Artery / metabolism
  • Infarction, Middle Cerebral Artery / pathology
  • Infarction, Middle Cerebral Artery / physiopathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Nerve Degeneration / metabolism*
  • Nerve Degeneration / pathology
  • Nerve Degeneration / physiopathology
  • Neuroglia / metabolism
  • Neuroglia / pathology
  • Neuroglia / ultrastructure
  • Neurons / metabolism*
  • Neurons / pathology
  • Neurons / ultrastructure
  • Phosphorylation
  • STAT3 Transcription Factor
  • Signal Transduction / physiology
  • Trans-Activators / metabolism*

Substances

  • Cytokines
  • DNA-Binding Proteins
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Trans-Activators