Interleukin-6 selectively enhances the intracellular calcium response to NMDA in developing CNS neurons

J Neurosci. 1995 Oct;15(10):6688-99. doi: 10.1523/JNEUROSCI.15-10-06688.1995.

Abstract

Increasing evidence supports a role for cytokines as chemical signals in the CNS, either under normal conditions or in the pathologic state. CNS levels of the cytokine interleukin-6 (IL-6) are known to be elevated in several diseases associated with developmental disorders and may contribute to the pathological state. To investigate the potential role of IL-6 in such disorders, neuronal effects of IL-6 were examined during development using an in vitro model system, cultured rat cerebellar granule neurons. The cultures were prepared from 8 d postnatal rat pups and exposed chronically to IL-6 (5 ng/ml) by addition to the culture medium. Neuronal effects of IL-6 were assessed by a comparison of calcium signals produced in control and IL-6 treated neurons by the glutamate receptor agonists NMDA and domoate and by K+ depolarization. IL-6 treatment significantly enhanced the response to NMDA and altered the developmental pattern of NMDA sensitivity, whereas only minor changes were observed for the response to domoate and K+. Reducing extracellular calcium and depleting intracellular stores significantly decreased the amplitude of the response to NMDA in control and IL-6 treated neurons. However, the IL-6 treated neurons were significantly more sensitive to these treatments than control neurons. These results suggest that elevated levels of IL-6 can significantly alter CNS neuron development and response to excitatory transmitters, and that IL-6 pretreatment selectively enhances the intracellular calcium responses to NMDA by altering the relative contribution of extracellular calcium influx and release of calcium from stores to the calcium signal.

Publication types

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

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cells, Cultured
  • Cerebellum / cytology
  • Cerebellum / metabolism*
  • Extracellular Space / metabolism
  • Interleukin-6 / pharmacology*
  • Intracellular Membranes / metabolism*
  • Kainic Acid / analogs & derivatives
  • Kainic Acid / pharmacology
  • N-Methylaspartate / pharmacology*
  • Neurons / metabolism
  • Potassium / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction

Substances

  • Interleukin-6
  • N-Methylaspartate
  • domoic acid
  • Potassium
  • Kainic Acid
  • Calcium