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Involvement of Spinal IL-6 Trans-Signaling in the Induction of Hyperexcitability of Deep Dorsal Horn Neurons by Spinal Tumor Necrosis Factor-Alpha.

Christian KönigEric MorchAnnett EitnerChristian MöllerBrian TurnquistHans-Georg SchaibleAndrea Ebersberger
Published in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2017)
Both spinal TNF-α and IL-6 induce a state of spinal hyperexcitability. We present the novel finding that the full effect of TNF-α on the development of spinal hyperexcitability depends on IL-6 trans-signaling acting downstream of TNF-α. IL-6 trans-signaling requires the formation of complexes of IL-6 and soluble IL-6 receptor. Spinal TNF-α furthers the release of IL-6 from neurons in the spinal cord during peripheral noxious stimulation and recruits microglial cells to provide soluble IL-6 receptor, which can form complexes with IL-6. Therefore, a specific interaction between neurons and microglia is required for the full development of TNF-α-induced hyperexcitability of nociceptive deep horsal horn neurons.
Keyphrases
  • spinal cord
  • neuropathic pain
  • rheumatoid arthritis
  • spinal cord injury
  • inflammatory response
  • drug induced
  • lps induced
  • endoplasmic reticulum stress