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pubmed-article:1851216pubmed:abstractTextWe 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.lld:pubmed
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pubmed-article:1851216pubmed:articleTitlePrimary culture of neonatal rat olfactory neurons.lld:pubmed
pubmed-article:1851216pubmed:affiliationDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.lld:pubmed
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pubmed-article:1851216pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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