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« Previous AbstractDifferences in development and cellular composition between neuronal cultures of rat accessory and main olfactory bulbs    Next AbstractAccessory olfactory bulb neurons are required for maintenance but not induction of V2R vomeronasal receptor gene expression in vitro »

Neuroscience


Title:Functional synapse formation between cultured rat accessory olfactory bulb neurons and vomeronasal pockets
Author(s):Muramoto K; Huang GZ; Taniguchi M; Kaba H;
Address:"Department of Integrative Physiology, Kochi Medical School, Kohasu, Oko-cho, Nankoku, Kochi 783-8505, Japan. tkazuyo@med.kochi-u.ac.jp"
Journal Title:Neuroscience
Year:2006
Volume:20060504
Issue:1
Page Number:475 - 486
DOI: 10.1016/j.neuroscience.2006.03.051
ISSN/ISBN:0306-4522 (Print) 0306-4522 (Linking)
Abstract:"To investigate the interaction between vomeronasal receptor neurons and accessory olfactory bulb neurons during pheromonal signal processing and specific synapse formation, partially dissociated rat vomeronasal receptor neurons were co-cultured with accessory olfactory bulb neurons. Between 7 and 14 days in co-culture, a few bundles of fibers from a spherical structure, termed the vomeronasal pocket, of cultured vomeronasal receptor neurons extended to the accessory olfactory bulb neurons. An optical recording of the intracellular Ca(2+) concentration was used to monitor the synaptic activation of cultured accessory olfactory bulb neurons. Electrical stimulation of the vomeronasal pocket between 7 and 14 days in co-culture had no effects on most of the cultured neurons tested, although it occasionally evoked weak responses in a small number of neurons. In contrast, vomeronasal pocket stimulation after 21 days in co-culture evoked clear calcium transients in a substantial number of cultured accessory olfactory bulb neurons. These responses of accessory olfactory bulb neurons were reversibly suppressed by the application of 6-cyano-7-nitroquinoxaline-2,3-dione; the calcium transients disappeared in most of the neurons and were diminished in the others. The application of d-2-amino-5-phosphonopentanoic acid partially affected the calcium transients, but blocked spontaneous calcium increases, which were observed repeatedly in accessory olfactory bulb-alone cultures. The application of both 6-cyano-7-nitroquinoxaline-2,3-dione and d-2-amino-5-phosphonopentanoic acid completely blocked the evoked calcium transients. These results suggest that functional glutamatergic synapses between vomeronasal receptor neurons and accessory olfactory bulb neurons were formed at around 21 days in co-culture"
Keywords:"2-Amino-5-phosphonovalerate/pharmacology 6-Cyano-7-nitroquinoxaline-2, 3-dione/pharmacology Animals Calcium/metabolism Cells, Cultured Coculture Techniques/methods Diagnostic Imaging/methods Electric Stimulation/methods Embryo, Mammalian Excitatory Amino A;neuroscience;"
Notes:"MedlineMuramoto, K Huang, G-Z Taniguchi, M Kaba, H eng Comparative Study Research Support, Non-U.S. Gov't 2006/05/09 Neuroscience. 2006 Aug 11; 141(1):475-86. doi: 10.1016/j.neuroscience.2006.03.051. Epub 2006 May 4"

 
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