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Synaptic organization of regenerated retina in the goldfish

dc.contributor.authorHitchcock, Peter F.en_US
dc.contributor.authorCirenza, Paulen_US
dc.date.accessioned2007-04-06T18:23:07Z
dc.date.available2007-04-06T18:23:07Z
dc.date.issued1994-05-22en_US
dc.identifier.citationHitchcock, Peter F.; Cirenza, Paul (1994)."Synaptic organization of regenerated retina in the goldfish." The Journal of Comparative Neurology 343(4): 609-616. <http://hdl.handle.net/2027.42/50060>en_US
dc.identifier.issn0021-9967en_US
dc.identifier.issn1096-9861en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/50060
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8034791&dopt=citationen_US
dc.description.abstractIn the adult goldfish, any manipulation that significantly depletes retinal neurons stimulates neurogenesis and the regeneration of nearly normal retina. We sought to determine the extent to which the regenerated neurons formed normal synaptic connections. We used qualitative and quantitative electron microscopy to compare the organization of the synaptic layers in regenerated and normal retinas. In eight eyes, a small patch of retina was surgically excised, stimulating regeneration of new retina in its place. Animals were killed 16–20 weeks after surgery. Qualitative comparisons of the synaptic architecture of photoreceptor terminals in the outer plexiform layer and quantitative comparisons of the synaptic organization in the inner plexiform layer were made between the patch of regenerated retina and an adjacent intact site. In the regenerated outer plexiform layer, cone pedicles and rod spherules were not arranged as regularly as normal, but they formed normal-appearing synaptic contacts. In the regenerated inner plexiform layer, with one exception, the quantitative descriptors of the synaptic organization in the normal and regenerate were n ot significantly different: The planimetric and numerical densities of the synapses, number of synapses/inner retinal neuron, and, with the exception of the bipolar terminals in the inner plexiform layer, and synapse depth profiles were similar. These data suggest that (1) relatively normal synaptic connections are recreated during regeneration, (2) the cellular mechanisms that guide synaptogenesis during development act during retinal regeneration, and (3) the physiological response properties of regenerated neurons should be comparable to that found in the normal retina. © 1994 Wiley-Liss, Inc.en_US
dc.format.extent1175130 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley-Liss, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherNeuroscience, Neurology and Psychiatryen_US
dc.titleSynaptic organization of regenerated retina in the goldfishen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Ophthalmology and Anatomy and Cell Biology, The University of Michigan School of Medicine, Ann Arbor, Michigan 48105 ; Kellogg Eye Center, 1000 Wall Street Ann Arbor, MI 48105en_US
dc.contributor.affiliationumDepartments of Ophthalmology and Anatomy and Cell Biology, The University of Michigan School of Medicine, Ann Arbor, Michigan 48105en_US
dc.identifier.pmid8034791en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/50060/1/903430410_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/cne.903430410en_US
dc.identifier.sourceThe Journal of Comparative Neurologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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