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Cellular and subcellular localization of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system

The cellular and subcellular distribution of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system was examined using antibodies against peptides corresponding to the C-terminal portions of AMPA receptor subunits: GluR1, GluR2/R3 and GluR4. The light and electron microscop...

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Published in:Brain research 1995-02, Vol.671 (1), p.83-94
Main Authors: Demêmes, Danielle, Lleixa, Annabel, Dechesne, Claude J.
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description The cellular and subcellular distribution of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system was examined using antibodies against peptides corresponding to the C-terminal portions of AMPA receptor subunits: GluR1, GluR2/R3 and GluR4. The light and electron microscopic immunocytochemical studies were carried out on Vibratome sections of rat and guinea pig vestibular sensory epithelia and ganglia. In the epithelium, GluR1 subunit immunoreactivity appeared as accumulations of patches outlining the baso-lateral periphery of the type I sensory cells. The GluR1-immunoreactive microareas were postsynaptically distributed on the membranes of calyceal afferent fibers. GluR2/R3 immunoreactivity was present in the sensory cells. GluR4 was not detected. In the vestibular ganglion, the neurons were densely stained with antibodies to GluR2/R3 and GluR4. The fibroblasts and the Schwann cells were also intensely stained with antibodies to GluR2/R3 and GluR4. In the sensory cells, the AMPA receptors, GluR2/R3, may function as (1) autoreceptors controlling afferent neurotransmitter release or (2) ‘postsynaptic’ receptors activated by the neurotransmitter release of the afferent calyx. The detection of GluR1 at postsynaptic sites in the afferent fibers provides anatomical evidence for the role of glutamate as a neurotransmitter of sensory cells. In the ganglion neurons, GluR2/R3 and GluR4 may represent reserve intracytoplasmic pools of receptor subunits in transit to the postsynaptic sites. In the Schwann cells, GluR2/R3 and GluR4 may be involved in neuronal-glial signalling at the nodes of Ranvier.
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The light and electron microscopic immunocytochemical studies were carried out on Vibratome sections of rat and guinea pig vestibular sensory epithelia and ganglia. In the epithelium, GluR1 subunit immunoreactivity appeared as accumulations of patches outlining the baso-lateral periphery of the type I sensory cells. The GluR1-immunoreactive microareas were postsynaptically distributed on the membranes of calyceal afferent fibers. GluR2/R3 immunoreactivity was present in the sensory cells. GluR4 was not detected. In the vestibular ganglion, the neurons were densely stained with antibodies to GluR2/R3 and GluR4. The fibroblasts and the Schwann cells were also intensely stained with antibodies to GluR2/R3 and GluR4. In the sensory cells, the AMPA receptors, GluR2/R3, may function as (1) autoreceptors controlling afferent neurotransmitter release or (2) ‘postsynaptic’ receptors activated by the neurotransmitter release of the afferent calyx. The detection of GluR1 at postsynaptic sites in the afferent fibers provides anatomical evidence for the role of glutamate as a neurotransmitter of sensory cells. In the ganglion neurons, GluR2/R3 and GluR4 may represent reserve intracytoplasmic pools of receptor subunits in transit to the postsynaptic sites. In the Schwann cells, GluR2/R3 and GluR4 may be involved in neuronal-glial signalling at the nodes of Ranvier.</description><subject>AMPA receptor</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Confocal microscopy</subject><subject>Epithelium - chemistry</subject><subject>Fibroblasts - chemistry</subject><subject>Fibroblasts - ultrastructure</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guinea pig</subject><subject>Guinea Pigs</subject><subject>Hair Cells, Vestibular - chemistry</subject><subject>Hair Cells, Vestibular - ultrastructure</subject><subject>Immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Electron</subject><subject>Motor control and motor pathways. Reflexes. Control centers of vegetative functions. 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Psychology</topic><topic>Guinea pig</topic><topic>Guinea Pigs</topic><topic>Hair Cells, Vestibular - chemistry</topic><topic>Hair Cells, Vestibular - ultrastructure</topic><topic>Immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Electron</topic><topic>Motor control and motor pathways. Reflexes. Control centers of vegetative functions. Vestibular system and equilibration</topic><topic>Rat</topic><topic>Rats</topic><topic>Receptors, AMPA - analysis</topic><topic>Rodentia</topic><topic>Schwann Cells - chemistry</topic><topic>Schwann Cells - ultrastructure</topic><topic>Space life sciences</topic><topic>Subcellular Fractions - chemistry</topic><topic>Subcellular Fractions - ultrastructure</topic><topic>Ultrastructure</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Vestibular Nuclei - chemistry</topic><topic>Vestibular Nuclei - ultrastructure</topic><topic>Vestibular system</topic><topic>Vestibule, Labyrinth - chemistry</topic><topic>Vestibule, Labyrinth - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Demêmes, Danielle</creatorcontrib><creatorcontrib>Lleixa, Annabel</creatorcontrib><creatorcontrib>Dechesne, Claude J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Demêmes, Danielle</au><au>Lleixa, Annabel</au><au>Dechesne, Claude J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular and subcellular localization of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1995-02-06</date><risdate>1995</risdate><volume>671</volume><issue>1</issue><spage>83</spage><epage>94</epage><pages>83-94</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>The cellular and subcellular distribution of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system was examined using antibodies against peptides corresponding to the C-terminal portions of AMPA receptor subunits: GluR1, GluR2/R3 and GluR4. The light and electron microscopic immunocytochemical studies were carried out on Vibratome sections of rat and guinea pig vestibular sensory epithelia and ganglia. In the epithelium, GluR1 subunit immunoreactivity appeared as accumulations of patches outlining the baso-lateral periphery of the type I sensory cells. The GluR1-immunoreactive microareas were postsynaptically distributed on the membranes of calyceal afferent fibers. GluR2/R3 immunoreactivity was present in the sensory cells. GluR4 was not detected. In the vestibular ganglion, the neurons were densely stained with antibodies to GluR2/R3 and GluR4. The fibroblasts and the Schwann cells were also intensely stained with antibodies to GluR2/R3 and GluR4. In the sensory cells, the AMPA receptors, GluR2/R3, may function as (1) autoreceptors controlling afferent neurotransmitter release or (2) ‘postsynaptic’ receptors activated by the neurotransmitter release of the afferent calyx. The detection of GluR1 at postsynaptic sites in the afferent fibers provides anatomical evidence for the role of glutamate as a neurotransmitter of sensory cells. In the ganglion neurons, GluR2/R3 and GluR4 may represent reserve intracytoplasmic pools of receptor subunits in transit to the postsynaptic sites. In the Schwann cells, GluR2/R3 and GluR4 may be involved in neuronal-glial signalling at the nodes of Ranvier.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>7728537</pmid><doi>10.1016/0006-8993(94)01322-9</doi><tpages>12</tpages></addata></record>
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source Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)
subjects AMPA receptor
Animals
Biological and medical sciences
Confocal microscopy
Epithelium - chemistry
Fibroblasts - chemistry
Fibroblasts - ultrastructure
Fluorescent Antibody Technique
Fundamental and applied biological sciences. Psychology
Guinea pig
Guinea Pigs
Hair Cells, Vestibular - chemistry
Hair Cells, Vestibular - ultrastructure
Immunocytochemistry
Immunohistochemistry
Microscopy, Confocal
Microscopy, Electron
Motor control and motor pathways. Reflexes. Control centers of vegetative functions. Vestibular system and equilibration
Rat
Rats
Receptors, AMPA - analysis
Rodentia
Schwann Cells - chemistry
Schwann Cells - ultrastructure
Space life sciences
Subcellular Fractions - chemistry
Subcellular Fractions - ultrastructure
Ultrastructure
Vertebrates: nervous system and sense organs
Vestibular Nuclei - chemistry
Vestibular Nuclei - ultrastructure
Vestibular system
Vestibule, Labyrinth - chemistry
Vestibule, Labyrinth - ultrastructure
title Cellular and subcellular localization of AMPA-selective glutamate receptors in the mammalian peripheral vestibular system
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