Satellite glial cells express IL-6 and corresponding signal-transducing receptors in the dorsal root ganglia of rat neuropathic pain model

Neuron Glia Biol. 2010 Feb;6(1):73-83. doi: 10.1017/S1740925X10000074. Epub 2010 Jun 2.

Abstract

There is a growing body of evidence that cytokines contribute to both induction and maintenance of neuropathic pain derived from changes in dorsal root ganglia (DRG), including the activity of the primary sensory neurons and their satellite glial cells (SGC). We used immunofluorescence and in situ hybridization methods to provide evidence that chronic constriction injury (CCI) of the sciatic nerve induces synthesis of interleukin-6 (IL-6) in SGC, elevation of IL-6 receptor (IL-6R) and activation of signal transducer and activator of transcription 3 (STAT3) signalling. Unilateral CCI of the rat sciatic nerve induced mechanoallodynia and thermal hyperalgesia in ipsilateral hind paws, but contralateral paws exhibited only temporal changes of sensitivity. We demonstrated that IL-6 mRNA and protein, which were expressed at very low levels in naïve DRG, were bilaterally increased not only in L4-L5 DRG neurons but also in SGC activated by unilateral CCI. Besides IL-6, substantial increase of IL-6R and pSTAT3 expression occurred in SGC following CCI, however, IL-6R associated protein, gp130 levels did not change. The results may suggest that unilateral CCI of the sciatic nerve induces bilateral activation of SGC in L4-L5 DRG to transduce IL-6 signalling during neuroinflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokine Receptor gp130 / genetics
  • Cytokine Receptor gp130 / metabolism
  • Disease Models, Animal
  • Functional Laterality
  • Ganglia, Spinal / pathology*
  • Ganglia, Spinal / physiopathology*
  • Gene Expression Regulation / physiology
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Male
  • Neuroglia / metabolism*
  • Pain Measurement
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Interleukin-6 / genetics
  • Receptors, Interleukin-6 / metabolism
  • STAT3 Transcription Factor / metabolism
  • Sciatic Neuropathy / pathology*
  • Sciatic Neuropathy / physiopathology
  • Signal Transduction / physiology*

Substances

  • Interleukin-6
  • RNA, Messenger
  • Receptors, Interleukin-6
  • STAT3 Transcription Factor
  • Cytokine Receptor gp130