Recent progress in the neurobiology of the vomeronasal organ
- 23 July 2002
- journal article
- review article
- Published by Wiley in Microscopy Research and Technique
- Vol. 58 (3) , 228-250
- https://doi.org/10.1002/jemt.10094
Abstract
In many terrestrial tetrapodes, a pair of vomeronasal organs (VNOs), which are chemosensory apparatuses, are situated at the base of the nasal septum in the anterior nasal cavity. The purposes of this review are to summarize comparative neuroanatomy and to introduce recent progress in neurobiological studies of the VNO. Five types of VNOs can be identifiable in terms of anatomical organization; snakes possess the most complex one. Sensory cells in the VNO, vomeronasal receptor neurons (VRNs), are located in its neuroepithelium, vomeronassal sensory epithelium. The VRNs retain the characteristic of epithelial cells in that they are born continuously from progenitor cells. They contain two prominent subcellular structures: microvilli and extraordinarily large amounts of smooth endoplasmic reticulum and a few unique glycoconjugates. The VRNs express two types of G‐protein ‐subunits: Giα2 and Goα and each of them is coupled with putative pheromone receptors, V1Rs and V2Rs, respectively. Recent physiological and biochemical studies have demonstrated that pheromones depolarize the V1R‐Giα2 and V2R‐Goα VRNs via IP3‐mediated mechanisms. The VRNs do not show adaptation and are ultrasensitive to putative pheromones. Other than being a chemosensory organ, the VNO and its primordium might play important roles for brain development; hypothalamic neurons that produce gonadotropin‐releasing hormone are born in the VNO primordium and a few other neuron‐like cells may be born in the VNO primordium and VNO. In human fetuses, anatomical findings strongly suggest that their VNOs contain a neuroepithelium. By contrast, it is unlikely that adult human VNO serves as a chemosensory organ. Microsc. Res. Tech. 58:228–250, 2002.Keywords
This publication has 171 references indexed in Scilit:
- Adenylyl Cyclase Activity in Turtle Vomeronasal and Olfactory EpitheliumBiochemical and Biophysical Research Communications, 1996
- Protein gene product 9.5 in the developing and mature rat vomeronasal organDevelopmental Brain Research, 1994
- Differential development of binding sites of two lectins in the vomeronasal axons of the rat accessory olfactory bulbDevelopmental Brain Research, 1994
- Voltage‐dependent Currents in Microvillar Receptor Cells of the Frog Vomeronasal OrganEuropean Journal of Neuroscience, 1993
- Immunolocalization of two cytochrome P450 isozymes in rat nasal chemosensory tissueNeuroReport, 1992
- Diversity of cell glycoconjugates shown histochemically: a perspective.Journal of Histochemistry & Cytochemistry, 1992
- Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode.Proceedings of the National Academy of Sciences, 1989
- Spatiotemporal cell expression of luteinizing hormone-releasing hormone in the prenatal mouse: evidence for an embryonic origin in the olfactory placodeDevelopmental Brain Research, 1989
- Origin of luteinizing hormone-releasing hormone neuronsNature, 1989
- The postnatal growth of the vomeronasal organ of the albino rat (Mus norvegicus albinus)Journal of Comparative Neurology, 1927