Primary culture of neonatal rat olfactory neurons

J Neurosci. 1991 May;11(5):1243-55. doi: 10.1523/JNEUROSCI.11-05-01243.1991.

Abstract

We have prepared primary cultures of purified neonatal rat olfactory neurons. Dissociated olfactory epithelial cells are maintained in modified Eagle's medium with D-valine, cytosine arabinoside, and NGF. NGF is required for neuronal survival. Immunohistochemical staining is positive for the neuronal markers vimentin, olfactory marker protein, and neuron-specific enolase, but negative for the glial markers, glial fibrillary acidic protein, and S-100 protein. Physiologic concentrations of odorants stimulate cAMP accumulation in the cells. Because of their morphology, biochemical composition, and responsiveness to odorants, these cells should enhance olfactory investigations.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Axons / drug effects
  • Axons / physiology
  • Biomarkers
  • Cell Survival / drug effects
  • Cells, Cultured
  • Culture Techniques / methods
  • Cyclic AMP / metabolism
  • Epithelial Cells
  • Nerve Growth Factors / pharmacology
  • Nerve Tissue Proteins / analysis
  • Neurons / cytology*
  • Neurons / drug effects
  • Neurons / physiology
  • Odorants
  • Phosphopyruvate Hydratase / analysis
  • Rats
  • Turbinates / cytology
  • Turbinates / innervation*
  • Vimentin / analysis

Substances

  • Biomarkers
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Vimentin
  • Cyclic AMP
  • Phosphopyruvate Hydratase