Chronic Odorant Exposure Upregulates Acquisition of Functional Properties in Cultured Embryonic Chick Olfactory Sensory Neurons.

Neuronal development and differentiation is modulated by activity‐dependent mechanisms that stimulate endogenous neurogenesis and differentiation to promote adaptive survival of the organism. Studies on bird odor imprinting have shown how sensory stimuli or environmental influences can affect neonatal behavior, presumably by remodeling the developing nervous system. It is unclear whether these changes originate from the sensory neurons themselves or from the brain. Thus, we attempted to address this by using an in vitro system to separate the peripheral neurons from their central connections. Olfactory neurons from embryonic day 17 Gallus domesticus chicks were isolated, cultured, and exposed to 100 µM amyl acetate or phenethyl alcohol in 12‐hr bouts, alternated with periods of no‐odor exposure. On days 4 and 5 in vitro, cells were immunostained for olfactory marker protein, neuron‐specific tubulin, and olfactory GTP‐binding protein, and tested for odorant sensitivity using calcium imaging. While odorant exposure did not result in a significant increase in the overall number of neurons, it promoted neuron differentiation: a larger proportion of odorant‐exposed cells expressed olfactory marker protein and the olfactory GTP‐binding protein. When cell responsiveness was tested using calcium imaging, a greater proportion of odorant‐exposed cells responded to stimulation with 100 µM amyl acetate or phenethyl alcohol. Thus, odorant exposure during development modulated the developmental trajectories of individual neurons, resulting in changes in protein expression associated with odorant signaling. This suggests that the neuronal changes in the periphery have an important contribution to the overall long‐term functional changes associated with odor imprinting. © 2016 Wiley Periodicals, Inc.