Activated microglia initiate motor neuron injury by a nitric oxide and glutamate-mediated mechanism

Weihua Zhao, Wenjie Xie, Weidong Le, David Beers, Yi He, Jenny S. Henkel, Ericka P. Greene, Albert A. Yen, Qin Xiao, Stanley H. Appel

Research output: Contribution to journalArticle

122 Scopus citations

Abstract

Recent studies suggest that motor neuron (MN) death may be non-cell autonomous, with cell injury mediated by interactions involving non-neuronal cells, such as microglia and astrocytes. To help define these interactions, we used primary MN cultures to investigate the effects of microglia activated by lipopolysaccharide or IgG immune complexes from patients with amyotrophic lateral sclerosis. Following activation, microglia induced MN injury, which was prevented by a microglial iNOS inhibitor as well as by catalase or glutathione. Glutamate was also required since inhibition of the MN AMPA/kainate receptor by CNQX prevented the toxic effects of activated microglia. Peroxynitrite and glutamate were synergistic in producing MN injury. Their toxic effects were also blocked by CNQX and prevented by calcium removal from the media. The addition of astrocytes to cocultures of MN and activated microglia prevented MN injury by removing glutamate from the media. The protective effects could be reversed by inhibiting astrocytic glutamate transport with dihydrokainic acid or pretreating astrocytes with H2O2. Astrocytic glutamate uptake was also decreased by activated microglia or by added peroxynitrite. These data suggest that free radicals released from activated microglia may initiate MN injury by increasing the susceptibility of the MN AMPA/kainate receptor to the toxic effects of glutamate.

Original languageEnglish (US)
Pages (from-to)964-977
Number of pages14
JournalJournal of Neuropathology and Experimental Neurology
Volume63
Issue number9
DOIs
StatePublished - Sep 2004

Keywords

  • AMPA/kainate receptors
  • Amyotrophic lateral sclerosis (ALS)
  • Astrocytes
  • Microglia
  • Motor neurons
  • Peroxynitrite

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Neuroscience(all)

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