IL-10 directly protects cortical neurons by activating PI-3 kinase and STAT-3 pathways

Brain Res. 2011 Feb 10:1373:189-94. doi: 10.1016/j.brainres.2010.11.096. Epub 2010 Dec 4.

Abstract

IL-10 reduces pro-inflammatory responses after ischemic stroke primarily by acting on glia and endothelium, but relatively little is known about the direct effects of IL-10 on cortical neurons, which are often damaged in stroke. We found by PCR and immunohistochemistry that cortical neurons express IL-10 receptor. Treatment of primary cortical neurons in culture with IL-10 increased neuronal survival after exposure to oxygen-glucose deprivation (OGD) or glutamate toxicity. IL-10 also induced phosphorylation of AKT in cortical neurons. Pretreatment with the specific PI-3K inhibitor, wortmannin, attenuated IL-10 mediated neuroprotection against OGD and glutamate. In addition, IL-10 induced STAT-3 phosphorylation. Pre-treatment with a functional blocking antibody to the IL-10 receptor reduced both Stat-3 and AKT phosphorylation and blocked IL-10 mediated protection of cortical neurons. These data suggest that IL-10 provides neuroprotection by acting via IL-10 receptor and PI3K/AKT and STAT-3 signal transduction pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Cell Death / drug effects
  • Cells, Cultured
  • Cerebral Cortex / cytology*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Embryo, Mammalian
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation / drug effects
  • Glucose / deficiency
  • Glutamic Acid / toxicity
  • Hypoxia
  • Interleukin-10 / pharmacology*
  • Neurons / drug effects*
  • Neurotoxins / toxicity
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Interleukin-18 / genetics
  • Receptors, Interleukin-18 / metabolism
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction / drug effects*
  • Tetrazolium Salts
  • Thiazoles
  • Tyrosine / metabolism

Substances

  • Enzyme Inhibitors
  • Neurotoxins
  • RNA, Messenger
  • Receptors, Interleukin-18
  • STAT3 Transcription Factor
  • Stat3 protein, rat
  • Tetrazolium Salts
  • Thiazoles
  • Interleukin-10
  • Glutamic Acid
  • Tyrosine
  • Phosphatidylinositol 3-Kinases
  • thiazolyl blue
  • Glucose