Regenerated optic fibers in goldfish reestablish a crude sectoral order in the visual pathway

The goldfish optic pathway is regenerated after an optic nerve crush. We have examined the axonal topography of the regenerated pathway by labeling, with horseradish peroxidase (HRP), axons originating from retinal sectors or annuli. The positions of the labeled axons in the cross section of the pat...

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Veröffentlicht in:Journal of comparative neurology (1911) 1988-11, Vol.277 (3), p.403-419
Hauptverfasser: Bernhardt, Robert, Easter Jr, Stephen S.
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description The goldfish optic pathway is regenerated after an optic nerve crush. We have examined the axonal topography of the regenerated pathway by labeling, with horseradish peroxidase (HRP), axons originating from retinal sectors or annuli. The positions of the labeled axons in the cross section of the pathway were compared to the normal and related to the factors that may influence axonal pathfinding. The positions of retinal axons in the cross section of the normal pathway are predictable from the retinal addresses of the ganglion cells described by the polar coordinates r (the distance from the optic disc) and θ (the sectoral or clockface position). The two coordinates map orthogonally onto the cross section of the pathway; r varies monotonically along one axis; θ varies along a perpendicular axis. The normal r‐order, present in the nonregenerated stump of the experimental nerve, was severely degraded and perhaps lost entirely in the regenerated optic nerve, tract, and brachia. Sectoral order was also lost as the axons passed the crush site, but it was reestablished, albeit crudely, in the regenerated tract and brachia where axons tended to occupy positions appropriate to their dorsal, ventral, nasal, and temporal retinal origins. The exit sequence of the regenerated axons from the stratum opticum into the tectal neuropil was normal: temporal first, nasal last. These results suggest that the regenerating fibers followed some θ specific cue located in the nonaxonal environment. It seems likely that the original axons probably followed the same cue. In contrast, the absence of r‐order suggests that there is no r‐specific cue for the regenerates to follow. It seems likely that the original r‐order was a consequence of nonspecific influences—the orderly spatiotemporal growth of the retina and the existence of a permissive region for axonal growth.
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We have examined the axonal topography of the regenerated pathway by labeling, with horseradish peroxidase (HRP), axons originating from retinal sectors or annuli. The positions of the labeled axons in the cross section of the pathway were compared to the normal and related to the factors that may influence axonal pathfinding. The positions of retinal axons in the cross section of the normal pathway are predictable from the retinal addresses of the ganglion cells described by the polar coordinates r (the distance from the optic disc) and θ (the sectoral or clockface position). The two coordinates map orthogonally onto the cross section of the pathway; r varies monotonically along one axis; θ varies along a perpendicular axis. The normal r‐order, present in the nonregenerated stump of the experimental nerve, was severely degraded and perhaps lost entirely in the regenerated optic nerve, tract, and brachia. Sectoral order was also lost as the axons passed the crush site, but it was reestablished, albeit crudely, in the regenerated tract and brachia where axons tended to occupy positions appropriate to their dorsal, ventral, nasal, and temporal retinal origins. The exit sequence of the regenerated axons from the stratum opticum into the tectal neuropil was normal: temporal first, nasal last. These results suggest that the regenerating fibers followed some θ specific cue located in the nonaxonal environment. It seems likely that the original axons probably followed the same cue. In contrast, the absence of r‐order suggests that there is no r‐specific cue for the regenerates to follow. 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Comp. Neurol</addtitle><description>The goldfish optic pathway is regenerated after an optic nerve crush. We have examined the axonal topography of the regenerated pathway by labeling, with horseradish peroxidase (HRP), axons originating from retinal sectors or annuli. The positions of the labeled axons in the cross section of the pathway were compared to the normal and related to the factors that may influence axonal pathfinding. The positions of retinal axons in the cross section of the normal pathway are predictable from the retinal addresses of the ganglion cells described by the polar coordinates r (the distance from the optic disc) and θ (the sectoral or clockface position). The two coordinates map orthogonally onto the cross section of the pathway; r varies monotonically along one axis; θ varies along a perpendicular axis. The normal r‐order, present in the nonregenerated stump of the experimental nerve, was severely degraded and perhaps lost entirely in the regenerated optic nerve, tract, and brachia. Sectoral order was also lost as the axons passed the crush site, but it was reestablished, albeit crudely, in the regenerated tract and brachia where axons tended to occupy positions appropriate to their dorsal, ventral, nasal, and temporal retinal origins. The exit sequence of the regenerated axons from the stratum opticum into the tectal neuropil was normal: temporal first, nasal last. These results suggest that the regenerating fibers followed some θ specific cue located in the nonaxonal environment. It seems likely that the original axons probably followed the same cue. In contrast, the absence of r‐order suggests that there is no r‐specific cue for the regenerates to follow. 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Psychology</subject><subject>Goldfish - anatomy &amp; histology</subject><subject>Horseradish Peroxidase</subject><subject>Nerve Crush</subject><subject>Nerve Regeneration</subject><subject>Neuronal Plasticity</subject><subject>Optic Nerve - analysis</subject><subject>Optic Nerve - anatomy &amp; histology</subject><subject>Optic Nerve - physiology</subject><subject>retinotectal system</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Visual Pathways - analysis</subject><subject>Visual Pathways - anatomy &amp; histology</subject><subject>Visual Pathways - physiology</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1v1DAQxS1EVZbCkSNSDohb2rGd-OOIVqWgli1CIE7Icpxx15BNtnZC2f8erzZacaKnGc37zczTI-QVhXMKwC5cj-camJTAQTwhCwpalFoJ-pQssk5LrYV8Rp6n9BMAtObqlJyySlAt6wX58QXvsMdoR2yLYTsGV_jQYExF6Iu7oWt9SOsiIqbRNt2-t4WLU4tFQjcO0XbFEFuMe3xcY_E7pCnPtnZcP9jdC3LibZfw5VzPyLf3l1-XH8qb26uPy3c3paskFyXzTDXKq4ZqX3nHOK-xBqgaB3WeA7hKOyZpBYJrpqRnzirwrAFoW2yQn5G3h7vbONxP2avZhOSw62yPw5SMVLWggotHQVpT4IyrDJYH0MUhpYjebGPY2LgzFMw-d5NzN8fcM_96Pjw1G2yP9Bx01t_Muk3Odj7a3oV0xCTUSnKaMXnAHkKHu___NMvV5b8GZsMhjfjnuGnjLyMkl7X5vroydfWJXn--VmbF_wK5XKoP</recordid><startdate>19881115</startdate><enddate>19881115</enddate><creator>Bernhardt, Robert</creator><creator>Easter Jr, Stephen S.</creator><general>Alan R. Liss, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>19881115</creationdate><title>Regenerated optic fibers in goldfish reestablish a crude sectoral order in the visual pathway</title><author>Bernhardt, Robert ; Easter Jr, Stephen S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4736-2f28b8f8b19f4fc2335e5004bc05b8f00c49c27140639287f2ca80f2b00ddebe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Animals</topic><topic>axonal guidance</topic><topic>axonal outgrowth</topic><topic>Axonal Transport</topic><topic>Axons - analysis</topic><topic>Axons - physiology</topic><topic>Biological and medical sciences</topic><topic>Brain Chemistry</topic><topic>Carassius auratus</topic><topic>Cyprinidae - anatomy &amp; histology</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Freshwater</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Goldfish - anatomy &amp; histology</topic><topic>Horseradish Peroxidase</topic><topic>Nerve Crush</topic><topic>Nerve Regeneration</topic><topic>Neuronal Plasticity</topic><topic>Optic Nerve - analysis</topic><topic>Optic Nerve - anatomy &amp; histology</topic><topic>Optic Nerve - physiology</topic><topic>retinotectal system</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Visual Pathways - analysis</topic><topic>Visual Pathways - anatomy &amp; histology</topic><topic>Visual Pathways - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bernhardt, Robert</creatorcontrib><creatorcontrib>Easter Jr, Stephen S.</creatorcontrib><collection>Istex</collection><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>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bernhardt, Robert</au><au>Easter Jr, Stephen S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regenerated optic fibers in goldfish reestablish a crude sectoral order in the visual pathway</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1988-11-15</date><risdate>1988</risdate><volume>277</volume><issue>3</issue><spage>403</spage><epage>419</epage><pages>403-419</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><coden>JCNEAM</coden><abstract>The goldfish optic pathway is regenerated after an optic nerve crush. We have examined the axonal topography of the regenerated pathway by labeling, with horseradish peroxidase (HRP), axons originating from retinal sectors or annuli. The positions of the labeled axons in the cross section of the pathway were compared to the normal and related to the factors that may influence axonal pathfinding. The positions of retinal axons in the cross section of the normal pathway are predictable from the retinal addresses of the ganglion cells described by the polar coordinates r (the distance from the optic disc) and θ (the sectoral or clockface position). The two coordinates map orthogonally onto the cross section of the pathway; r varies monotonically along one axis; θ varies along a perpendicular axis. The normal r‐order, present in the nonregenerated stump of the experimental nerve, was severely degraded and perhaps lost entirely in the regenerated optic nerve, tract, and brachia. Sectoral order was also lost as the axons passed the crush site, but it was reestablished, albeit crudely, in the regenerated tract and brachia where axons tended to occupy positions appropriate to their dorsal, ventral, nasal, and temporal retinal origins. The exit sequence of the regenerated axons from the stratum opticum into the tectal neuropil was normal: temporal first, nasal last. These results suggest that the regenerating fibers followed some θ specific cue located in the nonaxonal environment. It seems likely that the original axons probably followed the same cue. In contrast, the absence of r‐order suggests that there is no r‐specific cue for the regenerates to follow. It seems likely that the original r‐order was a consequence of nonspecific influences—the orderly spatiotemporal growth of the retina and the existence of a permissive region for axonal growth.</abstract><cop>New York</cop><pub>Alan R. Liss, Inc</pub><pmid>2461975</pmid><doi>10.1002/cne.902770306</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
axonal guidance
axonal outgrowth
Axonal Transport
Axons - analysis
Axons - physiology
Biological and medical sciences
Brain Chemistry
Carassius auratus
Cyprinidae - anatomy & histology
Eye and associated structures. Visual pathways and centers. Vision
Freshwater
Fundamental and applied biological sciences. Psychology
Goldfish - anatomy & histology
Horseradish Peroxidase
Nerve Crush
Nerve Regeneration
Neuronal Plasticity
Optic Nerve - analysis
Optic Nerve - anatomy & histology
Optic Nerve - physiology
retinotectal system
Vertebrates: nervous system and sense organs
Visual Pathways - analysis
Visual Pathways - anatomy & histology
Visual Pathways - physiology
title Regenerated optic fibers in goldfish reestablish a crude sectoral order in the visual pathway
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