Altered neuronal and microglial responses to excitotoxic and ischemic brain injury in mice lacking TNF receptors

Nat Med. 1996 Jul;2(7):788-94. doi: 10.1038/nm0796-788.

Abstract

Brain injury, as occurs in stroke or head trauma, induces a dramatic increase in levels of tumor necrosis factor-alpha (TNF), but its role in brain injury response is unknown. We generated mice genetically deficient in TNF receptors (TNFR-KO) to determine the role of TNF in brain cell injury responses. Damage to neurons caused by focal cerebral ischemia and epileptic seizures was exacerbated in TNFR-KO mice, indicating that TNF serves a neuroprotective function. Oxidative stress was increased and levels of an antioxidant enzyme reduced in brain cells of TNFR-KO mice, indicating that TNF protects neurons by stimulating antioxidant pathways. Injury-induced microglial activation was suppressed in TNFR-KO mice, demonstrating a key role for TNF in injury-induced immune response. Drugs that target TNF signaling pathways may prove beneficial in treating stroke and traumatic brain injury.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain Injuries / metabolism
  • Brain Injuries / pathology*
  • Brain Ischemia / metabolism
  • Brain Ischemia / pathology*
  • Cells, Cultured
  • Immunohistochemistry
  • Lipid Peroxidation
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Microglia / drug effects*
  • Microglia / metabolism
  • Microglia / pathology
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Neurotoxins / pharmacology*
  • Oxidative Stress
  • Receptors, Tumor Necrosis Factor / genetics*
  • Superoxide Dismutase / metabolism

Substances

  • Neurotoxins
  • Receptors, Tumor Necrosis Factor
  • Superoxide Dismutase