Light and electron microscopic demonstration of mGluR5 metabotropic glutamate receptor immunoreactive neuronal elements in the rat cerebellar cortex

The cellular and subcellular localization of the mGluR5 metabotropic glutamate receptor subtype was studied in the rat cerebellar cortex, by using the preembedding immunoperoxidase and immunogold techniques. Light microscopic observations revealed an abundant, intense labeling of neurons in the gran...

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Published in:Journal of comparative neurology (1911) Vol. 385; no. 4; pp. 641 - 650
Main Authors: Négyessy, L., Vidnyánszky, Z., Kuhn, R., Knöpfel, T., Görcs, T.J., Hámori, J.
Format: Journal Article
Language:English
Published: New York John Wiley & Sons, Inc 08-09-1997
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Summary:The cellular and subcellular localization of the mGluR5 metabotropic glutamate receptor subtype was studied in the rat cerebellar cortex, by using the preembedding immunoperoxidase and immunogold techniques. Light microscopic observations revealed an abundant, intense labeling of neurons in the granular layer as well as in the molecular layer. Lugaro and Golgi cells exhibited an intense mGluR5 immunoreactivity, while only a fraction of the neurons in the molecular layer were found to be mGluR5 immunopositive. In addition to a dense plexus of immunoreactive dendrites in the molecular layer of the cerebellar cortex, the mGluR5 immunopositive Golgi cell dendrites resembling axons at the light microscopic level were also labeled in the granular layer. At the ultrastructural level, mGluR5 immunoreactivity was present in neuronal elements postsynaptic to axon terminals of different morphology. By using a pre‐embedding immunogold method, it was found that mGluR5 immunoreactivity is accumulated at the plasma membranes extrasynaptically as well as at the periphery of the postsynaptic specializations, mainly of the parallel fiber synaptic contacts. These findings provide morphological evidence that mGluR5 is expressed by a population of neurons in the cerebellar cortex and can synaptically be activated via the parallel fiber system. J. Comp. Neurol. 385:641–650, 1997. © 1997 Wiley‐Liss, Inc.
Bibliography:Health Research Council Fund (ETT) - No. T-04 491/93
istex:7155A8B8FC562059BEBAB084FEB662D67D4B89D2
ArticleID:CNE9
ark:/67375/WNG-0C5G0B80-9
Hungarian National Research Fund (OTKA) - No. F-019289; No. T-016164; No. T-017282
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ISSN:0021-9967
1096-9861
DOI:10.1002/(SICI)1096-9861(19970908)385:4<641::AID-CNE9>3.0.CO;2-3