Neurochemical characteristics of a novel dorsal root ganglion X neuroblastoma hybrid cell line, F-11

J Neurochem. 1987 May;48(5):1624-31. doi: 10.1111/j.1471-4159.1987.tb05711.x.

Abstract

We investigated the properties of the novel dorsal root ganglion (DRG) hybrid cell line F-11 to see how closely these cells resembled normal DRG cells. Under normal growth conditions, F-11 cells appeared to contain several short neurite-like processes. However, these cells could also be grown under conditions in which they showed a much more extensive neuronal morphology, exhibiting many long neurites. Several differentiated features of DRG cells were present on F-11 cells. These included the presence of delta-opioid receptors, receptors for prostaglandins and bradykinin, and dihydropyridine-sensitive calcium channels. F-11 cells also synthesized and released a substance P-like compound, as determined by immunoreactivity. Both the number of bradykinin receptors and the voltage-sensitive calcium influx increased on cell differentiation. Opioid agonists (delta-specificity) were found to decrease cyclic AMP levels in F-11 cells in a naloxone- and pertussis toxin-reversible fashion. Bradykinin stimulated the synthesis of inositol-1,4-bisphosphate and inositol-1,4,5-trisphosphate. Ca2+ channel agonists stimulated voltage-sensitive Ca2+ influx in a dose-dependent, stereospecific manner, whereas Ca2+ channel antagonists inhibited Ca2+ influx. F-11 cells should, therefore, prove useful as models for authentic DRG neurons.

Publication types

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

MeSH terms

  • Animals
  • Cell Line
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Ion Channels / metabolism
  • Ion Channels / physiology
  • Neurons, Afferent / metabolism*
  • Receptors, Bradykinin
  • Receptors, Neurotransmitter / metabolism
  • Receptors, Opioid / metabolism
  • Substance P / metabolism

Substances

  • Ion Channels
  • Receptors, Bradykinin
  • Receptors, Neurotransmitter
  • Receptors, Opioid
  • Substance P