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Identification and localization of an immunoreactiveAMPA-type glutamate receptor subunit (GluR4) with respect to identified photoreceptor synapses in the outer plexiform layer of goldfish retina

dc.contributor.authorSchultz, K.en_US
dc.contributor.authorGoldman, Daniel J.en_US
dc.contributor.authorOhtsuka, T.en_US
dc.contributor.authorHirano, J.en_US
dc.contributor.authorStell, W. K.en_US
dc.date.accessioned2006-09-11T18:58:53Z
dc.date.available2006-09-11T18:58:53Z
dc.date.issued1997-10en_US
dc.identifier.citationSchultz, K.; Goldman, D. J.; Ohtsuka, T.; Hirano, J.; Stell, W. K.; (1997). "Identification and localization of an immunoreactiveAMPA-type glutamate receptor subunit (GluR4) with respect to identified photoreceptor synapses in the outer plexiform layer of goldfish retina." Journal of Neurocytology 26(10): 651-666. <http://hdl.handle.net/2027.42/47440>en_US
dc.identifier.issn0300-4864en_US
dc.identifier.issn1573-7381en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47440
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9368879&dopt=citationen_US
dc.description.abstractL-glutamate, the main excitatory synaptic transmitter in the retina, is released from photoreceptors and evokes responses in second-order retinal neurons (horizontal, bipolar cells) which utilize both ionotropic and metabotropic types of glutamate receptors. In the present study, to elucidate the functional roles of glutamate receptors in synaptic transmission, we have identified a specific ionotropic receptor subunit (GluR4) and determined its localization with respect to photoreceptor cells in the outer plexiform layer of the goldfish retina by light and pre-embedding electron-microscopical immunocytochemistry. We screened antisera to mammalian AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate)-preferring ionotropic glutamate receptors (GluR 1–4) of goldfish retina by light- and electron-microscopical immunocytochemistry. Only immunoreactive (IR) GluR4 was found in discrete clusters in the outer plexiform layer. The cones contacted in this manner were identified as long-wavelength (“red”) and intermediate-wavelength (“green”) cones, which were strongly immunoreactive to monoclonal antibody FRet 43 and antisera to goldfish red and green-cone opsins; and short-wavelength (“blue”) cones, which were weakly immunoreactive to FRet 43 but strongly immunoreactive with antiserum to blue-cone opsin. Immunoblots of goldfish retinal homogenate with anti-GluR4 revealed a single protein at Mr=110 kDa. Preadsorption of GluR4 antiserum with either the immunizing rat peptide, or its goldfish homolog, reduced or abolished staining in retinal sections and blots. Therefore, we have detected and localized genuine goldfish GluR4 in the outer plexiform layer of the goldfish retina. We characterized contacts between photoreceptor cells and GluR4-IR second-order neurons in the electron microscope. IR-GluR4 was localized to invaginating central dendrites of triads in ribbon synapses of red cones, semi-invaginating dendrites in other cones and rods, and dendrites making wide-cleft basal junctions in rods and cones; the GluR4-IR structures are best identified as dendrites of OFF-bipolar cells. The results of our studies indicate that in goldfish retina GluR4-expressing neurons are postsynaptic to all types of photoreceptors and that transmission from photoreceptors to OFF-bipolars is mediated at least in part by AMPA-sensitive receptors containing GluR4 subunits.en_US
dc.format.extent1360866 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Chapman and Hall ; Springer Science+Business Mediaen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherNeurosciencesen_US
dc.subject.otherNeuroradiologyen_US
dc.titleIdentification and localization of an immunoreactiveAMPA-type glutamate receptor subunit (GluR4) with respect to identified photoreceptor synapses in the outer plexiform layer of goldfish retinaen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute and Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationotherDepartment of Neurobiology, FB7, University of Oldenburg, P.O. Box 2503, 26111, Oldenburg, Germanyen_US
dc.contributor.affiliationotherDepartment of Biology, Toho University, Tokyoen_US
dc.contributor.affiliationotherInternational Marine Centre, Lungomare Eleonora d'Arborea, 22, 09072, Torregrande Oristano, Italyen_US
dc.contributor.affiliationotherLions' Sight Centre, Departments of Anatomy and SurgeryOphthalmology, and Neuroscience Research Group, University of Calgary Faculty of Medicine, 3330 Hospital Drive NW, Calgary, Alberta, Canada, T2N 4NIen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid9368879en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47440/1/11068_2004_Article_174105.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1018597811439en_US
dc.identifier.sourceJournal of Neurocytologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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