Olfactory receptors (OR) represent one of the largest gene families in the human genome. In spite of a significant progress
            in deciphering the physiological functions of olfactory receptors, how the majority of these G-protein-coupled receptors are
            activated is still mostly a mystery. Consequently, for the majority of OR genes there are currently no assigned physiological
            or behavioral functions. Deciphering ligand specificities and physiological significance of human ORs is important for understanding
            how the human olfactory genome encodes odors, and how such odors drive human behavior in health and disease. Although OR genes
            were originally thought to be restricted to the olfactory epithelium, several recent studies indicated that some members of
            the OR family might be acting outside the canonical chemosensory system. In a recent study, we have shown that the human airway
            epithelial cells can also act as chemosensory cells by directly sensing the inhalation of noxious bitter compounds, which
            can lead to increased mucociliary clearance, and hence may serve as a protective mechanism against inhaled toxins and microorganisms.
            Whether the airway epithelium can detect chemicals via other sensory pathways has not been reported to date. As a step in
            this direction, we describe methods for studying the cellular and subcellular localization of olfactory receptor proteins
            and mRNAs in human airways in both primary in vitro cultures and tissue sections.