Neuronal Soluble Fas Ligand Drives M1-Microglia Polarization after Cerebral Ischemia

CNS Neurosci Ther. 2016 Sep;22(9):771-81. doi: 10.1111/cns.12575. Epub 2016 Jun 10.

Abstract

Aims: This study explored sFasL expression in neurons and the potential role of neuronal sFasL in modulating the microglial phenotypes.

Methods: In vivo, middle cerebral artery occlusion (MCAO) was induced in both FasL-mutant (gld) and wild-type (wt) mice. In vitro, primary cortical neuron or microglia or coculture from wt/gld mice was subjected to oxygen glucose deprivation (OGD). sFasL level in the supernatant was evaluated by ELISA. Neuronal-conditioned medium (NCM) or exogenous sFasL was applied to primary microglia with or without FasL neutralizing antibody. Protein expression of JAK2/STAT3 and NF-κB pathways were determined by Western blot. The effect of microglia phenotype from wt/gld mice on the fate of ischemic neurons was further elucidated.

Results: In vivo, compared with wild-type mice, M1 markers (CD16, CD32 and iNOS) were attenuated in gld mice after MCAO. In vitro, post-OGD neuron released more sFasL. Both post-OGD NCM and exogenous sFasL could trigger M1-microglial polarization. However, this M1 phenotype shift was partially blocked by utilization of FasL neutralizing antibody or gld NCM. Consistently, JAK2/STAT3 and NF-κB signal pathways were both activated in microglia after exogenous sFasL treatment. Compared with wild-type mice, M1-conditioned medium prepared from gld mice protected neuron against OGD injury.

Conclusions: Ischemic neurons release sFasL, which contributes to M1-microglial polarization. The underlying mechanisms may involve the activation of JAK2/STAT3 and NF-κB signaling pathways.

Keywords: Inflammation; Ischemic stroke; Microglia; Neuron; Soluble FasL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Cell Hypoxia / genetics
  • Cell Polarity / genetics*
  • Cerebral Cortex / cytology
  • Culture Media, Conditioned / pharmacology
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Disease Models, Animal
  • Embryo, Mammalian
  • Fas Ligand Protein / genetics
  • Fas Ligand Protein / metabolism*
  • Gene Expression Regulation / genetics
  • Glucose / deficiency
  • Infarction, Middle Cerebral Artery / genetics*
  • Infarction, Middle Cerebral Artery / pathology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microglia / chemistry
  • Microglia / classification
  • Microglia / pathology*
  • Mutation / genetics
  • Neurons / drug effects
  • Neurons / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Signal Transduction / genetics

Substances

  • Antigens, CD
  • Culture Media, Conditioned
  • Fas Ligand Protein
  • Nitric Oxide Synthase Type II
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Glucose