
Ligand‐specific dose–response of heterologously expressed olfactory receptors
Author(s) -
Levasseur Grégoire,
Persuy MarieAnnick,
Grebert Denise,
Remy JeanJacques,
Salesse Roland,
PajotAugy Edith
Publication year - 2003
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1033.2003.03672.x
Subject(s) - receptor , stimulation , olfactory receptor , olfaction , biology , olfactory system , intracellular , ligand (biochemistry) , calcium in biology , adenylate kinase , microbiology and biotechnology , cyclase , biophysics , chemistry , biochemistry , medicine , endocrinology , neuroscience
Primary olfactory neuronal cultures exposed to odorant stimulation have previously exhibited concentration‐related effects in terms of intracellular cAMP levels and adenylate cyclase activity [Ronnett, G.V., Parfitt, D.J., Hester, L.D. & Snyder, S.H. (1991) PNAS 88 , 2366–2369]. Maximal stimulation occurred for intermediate concentrations, whereas AC activity declined for both low and high odorant concentrations. We suspected that this behavior might be ascribed to the intrinsic response of the first molecular species concerned by odorant detection, i.e. the olfactory receptor itself. In order to check this hypothesis, we developed an heterologous expression system in mammalian cells to characterize the functional response of receptors to odorants. Two mammalian olfactory receptors were used to initiate the study, the rat I7 olfactory receptor and the human OR17‐40 olfactory receptor. The cellular response of transfected cells to an odorant stimulation was tested by a spectrofluorimetric intracellular calcium assay, and proved in all cases to be dose‐dependent for the known ligands of these receptors, with an optimal response for intermediate concentrations. Further experiments were carried out with the rat I7 olfactory receptor, for which the sensitivity to an odorant, indicated by the concentration yielding the optimal calcium response, depended on the carbon chain length of the aldehydic odorant. The response is thus both ligand‐specific and dose‐dependent. We thus demonstrate that a differential dose–response originates from the olfactory receptor itself, which is thus capable of efficient discrimination between closely related agonists.