Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractFunctional synapse formation between cultured rat accessory olfactory bulb neurons and vomeronasal pockets    Next AbstractGlutathionylation and Reduction of Methacrolein in Tomato Plants Account for Its Absorption from the Vapor Phase »

Neurosci Lett


Title:Accessory olfactory bulb neurons are required for maintenance but not induction of V2R vomeronasal receptor gene expression in vitro
Author(s):Muramoto K; Hagino-Yamagishi K; Tonosaki K; Kaba H;
Address:"Division of Physiology, Department of Human Development and Fostering, Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama 350-0283, Japan. tkazuyo@dent.maikai.ac.jp"
Journal Title:Neurosci Lett
Year:2011
Volume:20110606
Issue:1
Page Number:6 - 9
DOI: 10.1016/j.neulet.2011.05.232
ISSN/ISBN:1872-7972 (Electronic) 0304-3940 (Linking)
Abstract:"Many mammals detect pheromones by a sensory organ, the vomeronasal organ (VNO). In a previous study using immunoblot and immunocytochemical analyses, we reported that cocultures of VNOs with accessory olfactory bulb (AOB) neurons resulted in the maturation of vomeronasal sensory neurons (VSNs) and a greater expression of V2R family vomeronasal receptors than cultures with VNO alone. To further characterize the V2R expression, we here investigated the time course of the expression of V2R mRNA in the presence or absence of AOB neurons using RT-PCR analysis. The expression of V2R mRNA was already detectable not only in the VNO cocultured with AOB neurons for 3 days in coculture but also in the VNO cultured alone for the same number of days. However, the expression of V2R mRNA in the VNO cultured alone was remarkably decreased during the additional culture period, although that in the cocultured VNO showed sustained expression. Moreover, the application of 2 muM TTX to the cocultured VNO resulted in a marked decrease in the V2R mRNA expression to a level equal to that in the VNO cultured alone for 14 days in coculture. Our previous working hypothesis was that the expression of V2Rs in VSNs was induced by interacting with AOB neurons. However, the present results suggest that the receptor expression in VSNs is independent of the interaction with AOB neurons in the early developmental stage, but is maintained by the active interaction with AOB neurons"
Keywords:"Animals Coculture Techniques Embryo, Mammalian/cytology Neurons/cytology/*metabolism Olfactory Bulb/cytology/*metabolism RNA, Messenger/metabolism Rats Rats, Wistar Receptors, Vasopressin/genetics/*metabolism Time Factors Vomeronasal Organ/cytology/metabo;"
Notes:"MedlineMuramoto, Kazuyo Hagino-Yamagishi, Kimiko Tonosaki, Keiichi Kaba, Hideto eng Research Support, Non-U.S. Gov't Ireland 2011/06/18 Neurosci Lett. 2011 Aug 1; 500(1):6-9. doi: 10.1016/j.neulet.2011.05.232. Epub 2011 Jun 6"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-11-2024