Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus

We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use γ‐amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of comparative neurology (1911) 1993-08, Vol.334 (4), p.618-630
Hauptverfasser: Cucchiaro, Josephine B., Uhlrich, Daniel J., Sherman, S. Murray
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 630
container_issue 4
container_start_page 618
container_title Journal of comparative neurology (1911)
container_volume 334
creator Cucchiaro, Josephine B.
Uhlrich, Daniel J.
Sherman, S. Murray
description We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use γ‐amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which they resemble other GABAergic terminals found in the geniculate neuropil (i.e., from geniculate interneurons and cells of the nearby perigeniculate nucleus). To do this, we labeled a population of pretectal axons with the anterograde tracer Phaseolus vulgaris leucoagglutinin and analyzed the morphology and synaptology of labeled pretectal terminals in the A laminae of the cat's lateral geniculate nucleus. The pretectal projection, which arises primarily from the nucleus of the optic tract (NOT), provides synaptic innervation to elements in the geniculate neuropil. The labeled NOT terminals are densely packed with vesicles, contain dark mitochondria, and form symmetrical synaptic contacts. These are characteristics of the F1 type of terminal, and we know from other studies that GABAergic axon terminals from interneurons and perigeniculate cells also give rise to F1 terminals. We compared our population of NOT terminals with labeled perigeniculate and unlabeled F1 terminals selected from the geniculate neuropil and found that all three populations share many morphological characteristics. Both qualitative and quantitative assessments of the pretectal terminals suggest that these are a type of F1 terminal. Most pretectal terminals selectively form synapses onto geniculate profiles that contain irregularly distributed vesicles and dark mitochondria and that are postsynaptic to other types of terminals. These postsynaptic targets thus exhibit features of another class of inhibitory, GABAergic terminal known as F2 terminals, which are the specialized appendages of geniculate interneurons. Pretectal inputs, being GABAergic, may thus serve to inhibit local interneuronal outputs. Pretectal axons also innervate the perigeniculate nucleus, in which the only targets are the other main type of inhibitory, GABAergic neurons. These results suggest that the pretectum may facilitate retinal transmission through the lateral geniculate nucleus by providing inhibition to the local inhibitory cells: the interneurons and probably perigeniculate cells. This would serve to release geniculate relay cells from inhibition. © 1993 Wiley‐Liss, Inc.
doi_str_mv 10.1002/cne.903340409
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75996092</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16736618</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4059-ffcfd4617b61c28174527af962740f3122782eea55a1a7e865fdbbf96bad82d53</originalsourceid><addsrcrecordid>eNqFkc1P3DAQxa0KBFvaY49IPsEpYDuJP45oBbQSgh4W0ZvlOGMIOMliO6L739fLrlY9wWk0837zNJqH0A9Kzigh7NwOcKZIWVakIuoLmlGieKEkp3tolnVaKMXFIfoa4zMhRKlSHqADWREpuJohd-9TMDGFyaYpAB4djqvBLCNE7MLY4_QEeBkgQdZ73A3vg4vCm74bzDu_HliTTiP2JkEwHj_C0Nlp3eFhsh6m-A3tO-MjfN_WI3R_dbmY_yxu7q5_zS9uCluRWhXOWddWnIqGU8skFVXNhHGKM1ERV1LGhGQApq4NNQIkr13bNFlvTCtZW5dH6GTjuwzj6wQx6b6LFrw3A4xT1KLO3yCKfQpSLkrOqcxgsQFtGGMM4PQydL0JK02JXgegcwB6F0Dmj7fGU9NDu6O3H8-62OhvnYfVx2Z6fnv5v_P2ki4m-LvbNOFF52NFrR9ur_XiQc0Xv_8wfVX-A0AMoWs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16736618</pqid></control><display><type>article</type><title>Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Cucchiaro, Josephine B. ; Uhlrich, Daniel J. ; Sherman, S. Murray</creator><creatorcontrib>Cucchiaro, Josephine B. ; Uhlrich, Daniel J. ; Sherman, S. Murray</creatorcontrib><description>We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use γ‐amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which they resemble other GABAergic terminals found in the geniculate neuropil (i.e., from geniculate interneurons and cells of the nearby perigeniculate nucleus). To do this, we labeled a population of pretectal axons with the anterograde tracer Phaseolus vulgaris leucoagglutinin and analyzed the morphology and synaptology of labeled pretectal terminals in the A laminae of the cat's lateral geniculate nucleus. The pretectal projection, which arises primarily from the nucleus of the optic tract (NOT), provides synaptic innervation to elements in the geniculate neuropil. The labeled NOT terminals are densely packed with vesicles, contain dark mitochondria, and form symmetrical synaptic contacts. These are characteristics of the F1 type of terminal, and we know from other studies that GABAergic axon terminals from interneurons and perigeniculate cells also give rise to F1 terminals. We compared our population of NOT terminals with labeled perigeniculate and unlabeled F1 terminals selected from the geniculate neuropil and found that all three populations share many morphological characteristics. Both qualitative and quantitative assessments of the pretectal terminals suggest that these are a type of F1 terminal. Most pretectal terminals selectively form synapses onto geniculate profiles that contain irregularly distributed vesicles and dark mitochondria and that are postsynaptic to other types of terminals. These postsynaptic targets thus exhibit features of another class of inhibitory, GABAergic terminal known as F2 terminals, which are the specialized appendages of geniculate interneurons. Pretectal inputs, being GABAergic, may thus serve to inhibit local interneuronal outputs. Pretectal axons also innervate the perigeniculate nucleus, in which the only targets are the other main type of inhibitory, GABAergic neurons. These results suggest that the pretectum may facilitate retinal transmission through the lateral geniculate nucleus by providing inhibition to the local inhibitory cells: the interneurons and probably perigeniculate cells. This would serve to release geniculate relay cells from inhibition. © 1993 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.903340409</identifier><identifier>PMID: 8408769</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; axon terminals ; Axons - chemistry ; Cats - anatomy &amp; histology ; Cats - metabolism ; GABA ; gamma-Aminobutyric Acid - analysis ; Geniculate Bodies - chemistry ; Geniculate Bodies - ultrastructure ; Microscopy, Electron ; Nerve Endings - chemistry ; NOT ; Synapses - chemistry ; Synapses - ultrastructure ; thalamus ; visual system</subject><ispartof>Journal of comparative neurology (1911), 1993-08, Vol.334 (4), p.618-630</ispartof><rights>Copyright © 1993 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4059-ffcfd4617b61c28174527af962740f3122782eea55a1a7e865fdbbf96bad82d53</citedby><cites>FETCH-LOGICAL-c4059-ffcfd4617b61c28174527af962740f3122782eea55a1a7e865fdbbf96bad82d53</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.903340409$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.903340409$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8408769$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cucchiaro, Josephine B.</creatorcontrib><creatorcontrib>Uhlrich, Daniel J.</creatorcontrib><creatorcontrib>Sherman, S. Murray</creatorcontrib><title>Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use γ‐amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which they resemble other GABAergic terminals found in the geniculate neuropil (i.e., from geniculate interneurons and cells of the nearby perigeniculate nucleus). To do this, we labeled a population of pretectal axons with the anterograde tracer Phaseolus vulgaris leucoagglutinin and analyzed the morphology and synaptology of labeled pretectal terminals in the A laminae of the cat's lateral geniculate nucleus. The pretectal projection, which arises primarily from the nucleus of the optic tract (NOT), provides synaptic innervation to elements in the geniculate neuropil. The labeled NOT terminals are densely packed with vesicles, contain dark mitochondria, and form symmetrical synaptic contacts. These are characteristics of the F1 type of terminal, and we know from other studies that GABAergic axon terminals from interneurons and perigeniculate cells also give rise to F1 terminals. We compared our population of NOT terminals with labeled perigeniculate and unlabeled F1 terminals selected from the geniculate neuropil and found that all three populations share many morphological characteristics. Both qualitative and quantitative assessments of the pretectal terminals suggest that these are a type of F1 terminal. Most pretectal terminals selectively form synapses onto geniculate profiles that contain irregularly distributed vesicles and dark mitochondria and that are postsynaptic to other types of terminals. These postsynaptic targets thus exhibit features of another class of inhibitory, GABAergic terminal known as F2 terminals, which are the specialized appendages of geniculate interneurons. Pretectal inputs, being GABAergic, may thus serve to inhibit local interneuronal outputs. Pretectal axons also innervate the perigeniculate nucleus, in which the only targets are the other main type of inhibitory, GABAergic neurons. These results suggest that the pretectum may facilitate retinal transmission through the lateral geniculate nucleus by providing inhibition to the local inhibitory cells: the interneurons and probably perigeniculate cells. This would serve to release geniculate relay cells from inhibition. © 1993 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>axon terminals</subject><subject>Axons - chemistry</subject><subject>Cats - anatomy &amp; histology</subject><subject>Cats - metabolism</subject><subject>GABA</subject><subject>gamma-Aminobutyric Acid - analysis</subject><subject>Geniculate Bodies - chemistry</subject><subject>Geniculate Bodies - ultrastructure</subject><subject>Microscopy, Electron</subject><subject>Nerve Endings - chemistry</subject><subject>NOT</subject><subject>Synapses - chemistry</subject><subject>Synapses - ultrastructure</subject><subject>thalamus</subject><subject>visual system</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1P3DAQxa0KBFvaY49IPsEpYDuJP45oBbQSgh4W0ZvlOGMIOMliO6L739fLrlY9wWk0837zNJqH0A9Kzigh7NwOcKZIWVakIuoLmlGieKEkp3tolnVaKMXFIfoa4zMhRKlSHqADWREpuJohd-9TMDGFyaYpAB4djqvBLCNE7MLY4_QEeBkgQdZ73A3vg4vCm74bzDu_HliTTiP2JkEwHj_C0Nlp3eFhsh6m-A3tO-MjfN_WI3R_dbmY_yxu7q5_zS9uCluRWhXOWddWnIqGU8skFVXNhHGKM1ERV1LGhGQApq4NNQIkr13bNFlvTCtZW5dH6GTjuwzj6wQx6b6LFrw3A4xT1KLO3yCKfQpSLkrOqcxgsQFtGGMM4PQydL0JK02JXgegcwB6F0Dmj7fGU9NDu6O3H8-62OhvnYfVx2Z6fnv5v_P2ki4m-LvbNOFF52NFrR9ur_XiQc0Xv_8wfVX-A0AMoWs</recordid><startdate>19930822</startdate><enddate>19930822</enddate><creator>Cucchiaro, Josephine B.</creator><creator>Uhlrich, Daniel J.</creator><creator>Sherman, S. Murray</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>19930822</creationdate><title>Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus</title><author>Cucchiaro, Josephine B. ; Uhlrich, Daniel J. ; Sherman, S. Murray</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4059-ffcfd4617b61c28174527af962740f3122782eea55a1a7e865fdbbf96bad82d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>axon terminals</topic><topic>Axons - chemistry</topic><topic>Cats - anatomy &amp; histology</topic><topic>Cats - metabolism</topic><topic>GABA</topic><topic>gamma-Aminobutyric Acid - analysis</topic><topic>Geniculate Bodies - chemistry</topic><topic>Geniculate Bodies - ultrastructure</topic><topic>Microscopy, Electron</topic><topic>Nerve Endings - chemistry</topic><topic>NOT</topic><topic>Synapses - chemistry</topic><topic>Synapses - ultrastructure</topic><topic>thalamus</topic><topic>visual system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cucchiaro, Josephine B.</creatorcontrib><creatorcontrib>Uhlrich, Daniel J.</creatorcontrib><creatorcontrib>Sherman, S. Murray</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>Cucchiaro, Josephine B.</au><au>Uhlrich, Daniel J.</au><au>Sherman, S. Murray</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1993-08-22</date><risdate>1993</risdate><volume>334</volume><issue>4</issue><spage>618</spage><epage>630</epage><pages>618-630</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use γ‐amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which they resemble other GABAergic terminals found in the geniculate neuropil (i.e., from geniculate interneurons and cells of the nearby perigeniculate nucleus). To do this, we labeled a population of pretectal axons with the anterograde tracer Phaseolus vulgaris leucoagglutinin and analyzed the morphology and synaptology of labeled pretectal terminals in the A laminae of the cat's lateral geniculate nucleus. The pretectal projection, which arises primarily from the nucleus of the optic tract (NOT), provides synaptic innervation to elements in the geniculate neuropil. The labeled NOT terminals are densely packed with vesicles, contain dark mitochondria, and form symmetrical synaptic contacts. These are characteristics of the F1 type of terminal, and we know from other studies that GABAergic axon terminals from interneurons and perigeniculate cells also give rise to F1 terminals. We compared our population of NOT terminals with labeled perigeniculate and unlabeled F1 terminals selected from the geniculate neuropil and found that all three populations share many morphological characteristics. Both qualitative and quantitative assessments of the pretectal terminals suggest that these are a type of F1 terminal. Most pretectal terminals selectively form synapses onto geniculate profiles that contain irregularly distributed vesicles and dark mitochondria and that are postsynaptic to other types of terminals. These postsynaptic targets thus exhibit features of another class of inhibitory, GABAergic terminal known as F2 terminals, which are the specialized appendages of geniculate interneurons. Pretectal inputs, being GABAergic, may thus serve to inhibit local interneuronal outputs. Pretectal axons also innervate the perigeniculate nucleus, in which the only targets are the other main type of inhibitory, GABAergic neurons. These results suggest that the pretectum may facilitate retinal transmission through the lateral geniculate nucleus by providing inhibition to the local inhibitory cells: the interneurons and probably perigeniculate cells. This would serve to release geniculate relay cells from inhibition. © 1993 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8408769</pmid><doi>10.1002/cne.903340409</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9967
ispartof Journal of comparative neurology (1911), 1993-08, Vol.334 (4), p.618-630
issn 0021-9967
1096-9861
language eng
recordid cdi_proquest_miscellaneous_75996092
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animals
axon terminals
Axons - chemistry
Cats - anatomy & histology
Cats - metabolism
GABA
gamma-Aminobutyric Acid - analysis
Geniculate Bodies - chemistry
Geniculate Bodies - ultrastructure
Microscopy, Electron
Nerve Endings - chemistry
NOT
Synapses - chemistry
Synapses - ultrastructure
thalamus
visual system
title Ultrastructure of synapses from the pretectum in the A-laminae of the cat's lateral geniculate nucleus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T04%3A18%3A21IST&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=Ultrastructure%20of%20synapses%20from%20the%20pretectum%20in%20the%20A-laminae%20of%20the%20cat's%20lateral%20geniculate%20nucleus&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Cucchiaro,%20Josephine%20B.&rft.date=1993-08-22&rft.volume=334&rft.issue=4&rft.spage=618&rft.epage=630&rft.pages=618-630&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.903340409&rft_dat=%3Cproquest_cross%3E16736618%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=16736618&rft_id=info:pmid/8408769&rfr_iscdi=true