Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats

Cortical feedback is the largest extraretinal projection to the lateral geniculate nucleus. This input is thought to modulate the transfer of visual information in a state‐dependent manner. The quantitative distribution and synaptology of axon terminals arising from different cortical areas is still...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of comparative neurology (1911) 1994-11, Vol.349 (2), p.259-268
Hauptverfasser: Vidnyanszky, Z, Hamori, J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 268
container_issue 2
container_start_page 259
container_title Journal of comparative neurology (1911)
container_volume 349
creator Vidnyanszky, Z
Hamori, J
description Cortical feedback is the largest extraretinal projection to the lateral geniculate nucleus. This input is thought to modulate the transfer of visual information in a state‐dependent manner. The quantitative distribution and synaptology of axon terminals arising from different cortical areas is still an unsolved question. To address this problem, the synaptic termination pattern of corticogeniculate axons from cortical areas 17 and 18 entering the lateral geniculate nucleus of the cat was examined. The Phaseolus vulgaris leucoagglutinin anterograde tract tracing method was used for the labeling of corticogeniculate terminals. Postsynaptic targets were characterized by postembedding γ‐aminobutyric acid (GABA) immunocytochemistry. In both laminae A and A1, labeled corticogeniculate axons from area 17 established synaptic contacts with GABA‐immunopositive, interneuronal dendritic profiles more frequently (17.5% of all axons) than did labeled axon terminals from area 18 (7% of axons). Conversely, 76% of labeled corticogeniculate axons from area 17, as opposed to 87% of labeled axons from area 18, terminated on GABA‐immunonegative relay cell dendrites. Furthermore, the mean diameter of GABA‐negative relay cell dendrites postsynaptic to labeled axons from area 17 was significantly smaller than the diameter of relay cell dendrites synapsing with labeled terminals from area 18. These results indicate that the corticogeniculate axons from cortical areas 17 and 18 exhibit different synaptic termination patterns in the dorsal lateral geniculate nucleus of the cat, suggesting that these two projections may subserve different functions in visual information processing. © 1994 Wiley‐Liss, Inc.
doi_str_mv 10.1002/cne.903490208
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77753180</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77753180</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3208-6f702eeed57ef50b66961b61452f8d69b5654b9f194bc351c337cefb6df3a23f3</originalsourceid><addsrcrecordid>eNqFkU-PFCEQxYnRrLOrR48mnLz1Cs00f4462V03WceYaDReCE0XinZDC7Q6n8EvLZOZTDzpqVL1fvUC9RB6QsklJaR9bgNcKsLWirRE3kMrShRvlOT0PlpVnTZKcfEQnef8lRCiFJNn6ExIToRsV-j328WE4osp_gdgGMGWFAOevE0x2zh7i00w4y77jKPDeRfMXOrQh3kp2KU4YRtTnZgRmwQmYyrqxoCpxCXi8gXwEFOu6mgKpFo_Q_B22Xc4LHaEJVczbE3Jj9ADZ8YMj4_1Ar2_vnq3edXcvbm53by4ayyrX2y4E6QFgKET4DrSc6447Tldd62TA1d9x7t1rxxV696yjlrGhAXX88Ex0zLHLtCzg--c4vcFctGTzxbG0QSIS9ZCiI5RSf4LUs6ppLKtYHMA91fLCZyek59M2mlK9D4lXVPSp5Qq__RovPQTDCf6GEvVxUH_6UfY_dtMb7ZXfzsfX-JzgV-nTZO-aS6Y6PSH7Y2W9OMncr19rV-yP5TQrs8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16618182</pqid></control><display><type>article</type><title>Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Vidnyanszky, Z ; Hamori, J</creator><creatorcontrib>Vidnyanszky, Z ; Hamori, J</creatorcontrib><description>Cortical feedback is the largest extraretinal projection to the lateral geniculate nucleus. This input is thought to modulate the transfer of visual information in a state‐dependent manner. The quantitative distribution and synaptology of axon terminals arising from different cortical areas is still an unsolved question. To address this problem, the synaptic termination pattern of corticogeniculate axons from cortical areas 17 and 18 entering the lateral geniculate nucleus of the cat was examined. The Phaseolus vulgaris leucoagglutinin anterograde tract tracing method was used for the labeling of corticogeniculate terminals. Postsynaptic targets were characterized by postembedding γ‐aminobutyric acid (GABA) immunocytochemistry. In both laminae A and A1, labeled corticogeniculate axons from area 17 established synaptic contacts with GABA‐immunopositive, interneuronal dendritic profiles more frequently (17.5% of all axons) than did labeled axon terminals from area 18 (7% of axons). Conversely, 76% of labeled corticogeniculate axons from area 17, as opposed to 87% of labeled axons from area 18, terminated on GABA‐immunonegative relay cell dendrites. Furthermore, the mean diameter of GABA‐negative relay cell dendrites postsynaptic to labeled axons from area 17 was significantly smaller than the diameter of relay cell dendrites synapsing with labeled terminals from area 18. These results indicate that the corticogeniculate axons from cortical areas 17 and 18 exhibit different synaptic termination patterns in the dorsal lateral geniculate nucleus of the cat, suggesting that these two projections may subserve different functions in visual information processing. © 1994 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.903490208</identifier><identifier>PMID: 7860782</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Cats - physiology ; Cerebral Cortex - physiology ; corticogeniculate ; Feedback ; gamma-aminobutyric acid ; Geniculate Bodies - physiology ; immunocytochemistry ; Immunohistochemistry ; Microscopy, Electron ; Neural Pathways - physiology ; Neural Pathways - ultrastructure ; Phaseolus vulgaris leucoagglutinin ; Phytohemagglutinins ; Presynaptic Terminals - physiology ; Presynaptic Terminals - ultrastructure ; thalamus</subject><ispartof>Journal of comparative neurology (1911), 1994-11, Vol.349 (2), p.259-268</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3208-6f702eeed57ef50b66961b61452f8d69b5654b9f194bc351c337cefb6df3a23f3</citedby><cites>FETCH-LOGICAL-c3208-6f702eeed57ef50b66961b61452f8d69b5654b9f194bc351c337cefb6df3a23f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcne.903490208$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.903490208$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7860782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vidnyanszky, Z</creatorcontrib><creatorcontrib>Hamori, J</creatorcontrib><title>Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Cortical feedback is the largest extraretinal projection to the lateral geniculate nucleus. This input is thought to modulate the transfer of visual information in a state‐dependent manner. The quantitative distribution and synaptology of axon terminals arising from different cortical areas is still an unsolved question. To address this problem, the synaptic termination pattern of corticogeniculate axons from cortical areas 17 and 18 entering the lateral geniculate nucleus of the cat was examined. The Phaseolus vulgaris leucoagglutinin anterograde tract tracing method was used for the labeling of corticogeniculate terminals. Postsynaptic targets were characterized by postembedding γ‐aminobutyric acid (GABA) immunocytochemistry. In both laminae A and A1, labeled corticogeniculate axons from area 17 established synaptic contacts with GABA‐immunopositive, interneuronal dendritic profiles more frequently (17.5% of all axons) than did labeled axon terminals from area 18 (7% of axons). Conversely, 76% of labeled corticogeniculate axons from area 17, as opposed to 87% of labeled axons from area 18, terminated on GABA‐immunonegative relay cell dendrites. Furthermore, the mean diameter of GABA‐negative relay cell dendrites postsynaptic to labeled axons from area 17 was significantly smaller than the diameter of relay cell dendrites synapsing with labeled terminals from area 18. These results indicate that the corticogeniculate axons from cortical areas 17 and 18 exhibit different synaptic termination patterns in the dorsal lateral geniculate nucleus of the cat, suggesting that these two projections may subserve different functions in visual information processing. © 1994 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Cats - physiology</subject><subject>Cerebral Cortex - physiology</subject><subject>corticogeniculate</subject><subject>Feedback</subject><subject>gamma-aminobutyric acid</subject><subject>Geniculate Bodies - physiology</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Electron</subject><subject>Neural Pathways - physiology</subject><subject>Neural Pathways - ultrastructure</subject><subject>Phaseolus vulgaris leucoagglutinin</subject><subject>Phytohemagglutinins</subject><subject>Presynaptic Terminals - physiology</subject><subject>Presynaptic Terminals - ultrastructure</subject><subject>thalamus</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-PFCEQxYnRrLOrR48mnLz1Cs00f4462V03WceYaDReCE0XinZDC7Q6n8EvLZOZTDzpqVL1fvUC9RB6QsklJaR9bgNcKsLWirRE3kMrShRvlOT0PlpVnTZKcfEQnef8lRCiFJNn6ExIToRsV-j328WE4osp_gdgGMGWFAOevE0x2zh7i00w4y77jKPDeRfMXOrQh3kp2KU4YRtTnZgRmwQmYyrqxoCpxCXi8gXwEFOu6mgKpFo_Q_B22Xc4LHaEJVczbE3Jj9ADZ8YMj4_1Ar2_vnq3edXcvbm53by4ayyrX2y4E6QFgKET4DrSc6447Tldd62TA1d9x7t1rxxV696yjlrGhAXX88Ex0zLHLtCzg--c4vcFctGTzxbG0QSIS9ZCiI5RSf4LUs6ppLKtYHMA91fLCZyek59M2mlK9D4lXVPSp5Qq__RovPQTDCf6GEvVxUH_6UfY_dtMb7ZXfzsfX-JzgV-nTZO-aS6Y6PSH7Y2W9OMncr19rV-yP5TQrs8</recordid><startdate>19941108</startdate><enddate>19941108</enddate><creator>Vidnyanszky, Z</creator><creator>Hamori, J</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>19941108</creationdate><title>Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats</title><author>Vidnyanszky, Z ; Hamori, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3208-6f702eeed57ef50b66961b61452f8d69b5654b9f194bc351c337cefb6df3a23f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Cats - physiology</topic><topic>Cerebral Cortex - physiology</topic><topic>corticogeniculate</topic><topic>Feedback</topic><topic>gamma-aminobutyric acid</topic><topic>Geniculate Bodies - physiology</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Microscopy, Electron</topic><topic>Neural Pathways - physiology</topic><topic>Neural Pathways - ultrastructure</topic><topic>Phaseolus vulgaris leucoagglutinin</topic><topic>Phytohemagglutinins</topic><topic>Presynaptic Terminals - physiology</topic><topic>Presynaptic Terminals - ultrastructure</topic><topic>thalamus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vidnyanszky, Z</creatorcontrib><creatorcontrib>Hamori, J</creatorcontrib><collection>Istex</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>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vidnyanszky, Z</au><au>Hamori, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1994-11-08</date><risdate>1994</risdate><volume>349</volume><issue>2</issue><spage>259</spage><epage>268</epage><pages>259-268</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Cortical feedback is the largest extraretinal projection to the lateral geniculate nucleus. This input is thought to modulate the transfer of visual information in a state‐dependent manner. The quantitative distribution and synaptology of axon terminals arising from different cortical areas is still an unsolved question. To address this problem, the synaptic termination pattern of corticogeniculate axons from cortical areas 17 and 18 entering the lateral geniculate nucleus of the cat was examined. The Phaseolus vulgaris leucoagglutinin anterograde tract tracing method was used for the labeling of corticogeniculate terminals. Postsynaptic targets were characterized by postembedding γ‐aminobutyric acid (GABA) immunocytochemistry. In both laminae A and A1, labeled corticogeniculate axons from area 17 established synaptic contacts with GABA‐immunopositive, interneuronal dendritic profiles more frequently (17.5% of all axons) than did labeled axon terminals from area 18 (7% of axons). Conversely, 76% of labeled corticogeniculate axons from area 17, as opposed to 87% of labeled axons from area 18, terminated on GABA‐immunonegative relay cell dendrites. Furthermore, the mean diameter of GABA‐negative relay cell dendrites postsynaptic to labeled axons from area 17 was significantly smaller than the diameter of relay cell dendrites synapsing with labeled terminals from area 18. These results indicate that the corticogeniculate axons from cortical areas 17 and 18 exhibit different synaptic termination patterns in the dorsal lateral geniculate nucleus of the cat, suggesting that these two projections may subserve different functions in visual information processing. © 1994 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7860782</pmid><doi>10.1002/cne.903490208</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9967
ispartof Journal of comparative neurology (1911), 1994-11, Vol.349 (2), p.259-268
issn 0021-9967
1096-9861
language eng
recordid cdi_proquest_miscellaneous_77753180
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animals
Cats - physiology
Cerebral Cortex - physiology
corticogeniculate
Feedback
gamma-aminobutyric acid
Geniculate Bodies - physiology
immunocytochemistry
Immunohistochemistry
Microscopy, Electron
Neural Pathways - physiology
Neural Pathways - ultrastructure
Phaseolus vulgaris leucoagglutinin
Phytohemagglutinins
Presynaptic Terminals - physiology
Presynaptic Terminals - ultrastructure
thalamus
title Quantitative electron microscopic analysis of synaptic input from cortical areas 17 and 18 to the dorsal lateral geniculate nucleus in cats
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T16%3A48%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Quantitative%20electron%20microscopic%20analysis%20of%20synaptic%20input%20from%20cortical%20areas%2017%20and%2018%20to%20the%20dorsal%20lateral%20geniculate%20nucleus%20in%20cats&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Vidnyanszky,%20Z&rft.date=1994-11-08&rft.volume=349&rft.issue=2&rft.spage=259&rft.epage=268&rft.pages=259-268&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.903490208&rft_dat=%3Cproquest_cross%3E77753180%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16618182&rft_id=info:pmid/7860782&rfr_iscdi=true