A novel brain receptor is expressed in a distinct population of olfactory sensory neurons

Three novel G‐protein‐coupled receptor genes related to the previously described RA1c gene have been isolated from the mouse genome. Expression of these genes has been detected in distinct areas of the brain and also in the olfactory epithelium of the nose. Developmental studies revealed a different...

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Bibliographic Details
Published in:The European journal of neuroscience Vol. 12; no. 11; pp. 3926 - 3934
Main Authors: Conzelmann, Sidonie, Levai, Olga, Bode, Barbara, Eisel, Ulrich, Raming, Klaus, Breer, Heinz, Strotmann, Jörg
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Science Ltd 01-11-2000
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Summary:Three novel G‐protein‐coupled receptor genes related to the previously described RA1c gene have been isolated from the mouse genome. Expression of these genes has been detected in distinct areas of the brain and also in the olfactory epithelium of the nose. Developmental studies revealed a differential onset of expression: in the brain at embryonic stage 17, in the olfactory system at stage E12. In order to determine which cell type in the olfactory epithelium expresses this unique receptor type, a transgenic approach was employed which allowed a coexpression of histological markers together with the receptor and thus visualization of the appropriate cell population. It was found that the receptor‐expressing cells were located very close to the basal membrane of the epithelium; however, the cells extended a dendritic process to the epithelial surface and their axons projected into the main olfactory bulb where they converged onto two or three glomeruli in the dorsal and posterior region of the bulb. Thus, these data provide evidence that this unique type of receptor is expressed in mature olfactory neurons and suggests that it may be involved in the detection of special odour molecules.
Bibliography:ark:/67375/WNG-KC4P68TG-G
istex:3AEBC39DC240375914623BF415DF266307150AEC
ArticleID:EJN286
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0953-816X
1460-9568
DOI:10.1046/j.1460-9568.2000.00286.x