Horizontal eye movement networks in primates as revealed by retrograde transneuronal transfer of rabies virus: Differences in monosynaptic input to "slow" and "fast" abducens motoneurons
The sources of monosynaptic input to “fast” and “slow” abducens motoneurons (MNs) were revealed in primates by retrograde transneuronal tracing with rabies virus after injection either into the distal or central portions of the lateral rectus (LR) muscle, containing, respectively, “en grappe” endpla...
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Veröffentlicht in: | Journal of comparative neurology (1911) 2006-10, Vol.498 (6), p.762-785 |
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container_title | Journal of comparative neurology (1911) |
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creator | Ugolini, Gabriella Klam, François Doldan Dans, Maria Dubayle, David Brandi, Anne-Marie Büttner-Ennever, Jean Graf, Werner |
description | The sources of monosynaptic input to “fast” and “slow” abducens motoneurons (MNs) were revealed in primates by retrograde transneuronal tracing with rabies virus after injection either into the distal or central portions of the lateral rectus (LR) muscle, containing, respectively, “en grappe” endplates innervating slow muscle fibers or “en plaque” motor endplates innervating fast fibers. Rabies uptake involved exclusively motor endplates within the injected portion of the muscle. At 2.5 days after injections, remarkable differences of innervation of slow and fast MNs were demonstrated. Premotor connectivity of slow MNs, revealed here for the first time, involves mainly the supraoculomotor area, central mesencephalic reticular formation, and portions of medial vestibular and prepositus hypoglossi nuclei carrying eye position and smooth pursuit signals. Results suggest that slow MNs are involved exclusively in slow eye movements (vergence and possibly smooth pursuit), muscle length stabilization and gaze holding (fixation), and rule out their participation in fast eye movements (saccades, vestibulo‐ocular reflex). By contrast, all known monosynaptic pathways to LR MNs innervate fast MNs, showing their participation in the entire horizontal eye movements repertoire. Hitherto unknown monosynaptic connections were also revealed, such as those derived from the central mesencephalic reticular formation and vertical eye movements pathways (Y group, interstitial nucleus of Cajal, rostral interstitial nucleus of the medial longitudinal fasciculus). The different connectivity of fast and slow MNs parallel differences in properties of muscle fibers that they innervate, suggesting that muscle fibers properties, rather than being self‐determined, are the result of differences of their premotor innervation. J. Comp. Neurol. 498:762–785, 2006. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cne.21092 |
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Rabies uptake involved exclusively motor endplates within the injected portion of the muscle. At 2.5 days after injections, remarkable differences of innervation of slow and fast MNs were demonstrated. Premotor connectivity of slow MNs, revealed here for the first time, involves mainly the supraoculomotor area, central mesencephalic reticular formation, and portions of medial vestibular and prepositus hypoglossi nuclei carrying eye position and smooth pursuit signals. Results suggest that slow MNs are involved exclusively in slow eye movements (vergence and possibly smooth pursuit), muscle length stabilization and gaze holding (fixation), and rule out their participation in fast eye movements (saccades, vestibulo‐ocular reflex). By contrast, all known monosynaptic pathways to LR MNs innervate fast MNs, showing their participation in the entire horizontal eye movements repertoire. Hitherto unknown monosynaptic connections were also revealed, such as those derived from the central mesencephalic reticular formation and vertical eye movements pathways (Y group, interstitial nucleus of Cajal, rostral interstitial nucleus of the medial longitudinal fasciculus). The different connectivity of fast and slow MNs parallel differences in properties of muscle fibers that they innervate, suggesting that muscle fibers properties, rather than being self‐determined, are the result of differences of their premotor innervation. J. Comp. Neurol. 498:762–785, 2006. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.21092</identifier><identifier>PMID: 16927266</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Abducens Nerve ; Abducens Nerve - cytology ; Abducens Nerve - virology ; Animals ; Brain Stem ; Brain Stem - cytology ; Brain Stem - virology ; Eye Movements ; Female ; fixation ; Image Processing, Computer-Assisted ; Immunohistochemistry ; Life Sciences ; Macaca mulatta ; Motor Neurons ; Motor Neurons - cytology ; Motor Neurons - virology ; Neurons and Cognition ; Oculomotor Muscles ; Oculomotor Muscles - innervation ; Primates ; Rabies virus ; saccades ; smooth pursuit ; vergence ; vestibulo-ocular</subject><ispartof>Journal of comparative neurology (1911), 2006-10, Vol.498 (6), p.762-785</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4572-8f4fc20527ad99e04aa6cb0d5cd35c69e0d531d2be9b3622355bb42d02d826b03</citedby><cites>FETCH-LOGICAL-c4572-8f4fc20527ad99e04aa6cb0d5cd35c69e0d531d2be9b3622355bb42d02d826b03</cites><orcidid>0000-0003-0040-856X</orcidid></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.21092$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.21092$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16927266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00094389$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ugolini, Gabriella</creatorcontrib><creatorcontrib>Klam, François</creatorcontrib><creatorcontrib>Doldan Dans, Maria</creatorcontrib><creatorcontrib>Dubayle, David</creatorcontrib><creatorcontrib>Brandi, Anne-Marie</creatorcontrib><creatorcontrib>Büttner-Ennever, Jean</creatorcontrib><creatorcontrib>Graf, Werner</creatorcontrib><title>Horizontal eye movement networks in primates as revealed by retrograde transneuronal transfer of rabies virus: Differences in monosynaptic input to "slow" and "fast" abducens motoneurons</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>The sources of monosynaptic input to “fast” and “slow” abducens motoneurons (MNs) were revealed in primates by retrograde transneuronal tracing with rabies virus after injection either into the distal or central portions of the lateral rectus (LR) muscle, containing, respectively, “en grappe” endplates innervating slow muscle fibers or “en plaque” motor endplates innervating fast fibers. Rabies uptake involved exclusively motor endplates within the injected portion of the muscle. At 2.5 days after injections, remarkable differences of innervation of slow and fast MNs were demonstrated. Premotor connectivity of slow MNs, revealed here for the first time, involves mainly the supraoculomotor area, central mesencephalic reticular formation, and portions of medial vestibular and prepositus hypoglossi nuclei carrying eye position and smooth pursuit signals. Results suggest that slow MNs are involved exclusively in slow eye movements (vergence and possibly smooth pursuit), muscle length stabilization and gaze holding (fixation), and rule out their participation in fast eye movements (saccades, vestibulo‐ocular reflex). By contrast, all known monosynaptic pathways to LR MNs innervate fast MNs, showing their participation in the entire horizontal eye movements repertoire. Hitherto unknown monosynaptic connections were also revealed, such as those derived from the central mesencephalic reticular formation and vertical eye movements pathways (Y group, interstitial nucleus of Cajal, rostral interstitial nucleus of the medial longitudinal fasciculus). The different connectivity of fast and slow MNs parallel differences in properties of muscle fibers that they innervate, suggesting that muscle fibers properties, rather than being self‐determined, are the result of differences of their premotor innervation. J. Comp. Neurol. 498:762–785, 2006. © 2006 Wiley‐Liss, Inc.</description><subject>Abducens Nerve</subject><subject>Abducens Nerve - cytology</subject><subject>Abducens Nerve - virology</subject><subject>Animals</subject><subject>Brain Stem</subject><subject>Brain Stem - cytology</subject><subject>Brain Stem - virology</subject><subject>Eye Movements</subject><subject>Female</subject><subject>fixation</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunohistochemistry</subject><subject>Life Sciences</subject><subject>Macaca mulatta</subject><subject>Motor Neurons</subject><subject>Motor Neurons - cytology</subject><subject>Motor Neurons - virology</subject><subject>Neurons and Cognition</subject><subject>Oculomotor Muscles</subject><subject>Oculomotor Muscles - innervation</subject><subject>Primates</subject><subject>Rabies virus</subject><subject>saccades</subject><subject>smooth pursuit</subject><subject>vergence</subject><subject>vestibulo-ocular</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkstu1DAUhiMEokNhwQsgaxZILNLaTuLE7KqhdBCjQaq47SzHPgHTxB5sZ4bh0Xg6PBfaFYLVufg7v4-O_ix7SvAZwZieKwtnlGBO72WTFFjOG0buZ5P0RnLOWX2SPQrhG8aY86J5mJ0QxmlNGZtkv-bOm5_ORtkj2AIa3BoGsBFZiBvnbwIyFq28GWSEgGRAHtYge9Co3aY8evfFSw0oemmDhdE7m5T2VQceuQ552Zo0ujZ-DC_RK9OlPlgFe-XBWRe2Vq6iUalejRFFh6ahd5spklajaSdDTGmrRwU2pIHoDt-Ex9mDTvYBnhzjafbh9eX72TxfvLt6M7tY5Kqsapo3XdkpiitaS8054FJKplqsK6WLSrHU0VVBNG2BtwWjtKiqti2pxlQ3lLW4OM1eHHS_yl7sT-G3wkkj5hcLsevt7loWDV-TxD4_sCvvvo8QohhMUND30oIbg2BNzauqwf8ECa9rVpXlf4EUF_Xdmsq7EDx0t7sSLHY2EckmYm-TxD47io7tAPqOPPoiAecHYGN62P5dScyWl38k88OECRF-3E5IfyNYXdSV-LS8Etef3y4_4tm1IMVvfxDZew</recordid><startdate>20061020</startdate><enddate>20061020</enddate><creator>Ugolini, Gabriella</creator><creator>Klam, François</creator><creator>Doldan Dans, Maria</creator><creator>Dubayle, David</creator><creator>Brandi, Anne-Marie</creator><creator>Büttner-Ennever, Jean</creator><creator>Graf, Werner</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</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>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-0040-856X</orcidid></search><sort><creationdate>20061020</creationdate><title>Horizontal eye movement networks in primates as revealed by retrograde transneuronal transfer of rabies virus: Differences in monosynaptic input to "slow" and "fast" abducens motoneurons</title><author>Ugolini, Gabriella ; Klam, François ; Doldan Dans, Maria ; Dubayle, David ; Brandi, Anne-Marie ; Büttner-Ennever, Jean ; Graf, Werner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4572-8f4fc20527ad99e04aa6cb0d5cd35c69e0d531d2be9b3622355bb42d02d826b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Abducens Nerve</topic><topic>Abducens Nerve - cytology</topic><topic>Abducens Nerve - virology</topic><topic>Animals</topic><topic>Brain Stem</topic><topic>Brain Stem - cytology</topic><topic>Brain Stem - virology</topic><topic>Eye Movements</topic><topic>Female</topic><topic>fixation</topic><topic>Image Processing, Computer-Assisted</topic><topic>Immunohistochemistry</topic><topic>Life Sciences</topic><topic>Macaca mulatta</topic><topic>Motor Neurons</topic><topic>Motor Neurons - cytology</topic><topic>Motor Neurons - virology</topic><topic>Neurons and Cognition</topic><topic>Oculomotor Muscles</topic><topic>Oculomotor Muscles - innervation</topic><topic>Primates</topic><topic>Rabies virus</topic><topic>saccades</topic><topic>smooth pursuit</topic><topic>vergence</topic><topic>vestibulo-ocular</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ugolini, Gabriella</creatorcontrib><creatorcontrib>Klam, François</creatorcontrib><creatorcontrib>Doldan Dans, Maria</creatorcontrib><creatorcontrib>Dubayle, David</creatorcontrib><creatorcontrib>Brandi, Anne-Marie</creatorcontrib><creatorcontrib>Büttner-Ennever, Jean</creatorcontrib><creatorcontrib>Graf, Werner</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ugolini, Gabriella</au><au>Klam, François</au><au>Doldan Dans, Maria</au><au>Dubayle, David</au><au>Brandi, Anne-Marie</au><au>Büttner-Ennever, Jean</au><au>Graf, Werner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Horizontal eye movement networks in primates as revealed by retrograde transneuronal transfer of rabies virus: Differences in monosynaptic input to "slow" and "fast" abducens motoneurons</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2006-10-20</date><risdate>2006</risdate><volume>498</volume><issue>6</issue><spage>762</spage><epage>785</epage><pages>762-785</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>The sources of monosynaptic input to “fast” and “slow” abducens motoneurons (MNs) were revealed in primates by retrograde transneuronal tracing with rabies virus after injection either into the distal or central portions of the lateral rectus (LR) muscle, containing, respectively, “en grappe” endplates innervating slow muscle fibers or “en plaque” motor endplates innervating fast fibers. Rabies uptake involved exclusively motor endplates within the injected portion of the muscle. At 2.5 days after injections, remarkable differences of innervation of slow and fast MNs were demonstrated. Premotor connectivity of slow MNs, revealed here for the first time, involves mainly the supraoculomotor area, central mesencephalic reticular formation, and portions of medial vestibular and prepositus hypoglossi nuclei carrying eye position and smooth pursuit signals. Results suggest that slow MNs are involved exclusively in slow eye movements (vergence and possibly smooth pursuit), muscle length stabilization and gaze holding (fixation), and rule out their participation in fast eye movements (saccades, vestibulo‐ocular reflex). By contrast, all known monosynaptic pathways to LR MNs innervate fast MNs, showing their participation in the entire horizontal eye movements repertoire. Hitherto unknown monosynaptic connections were also revealed, such as those derived from the central mesencephalic reticular formation and vertical eye movements pathways (Y group, interstitial nucleus of Cajal, rostral interstitial nucleus of the medial longitudinal fasciculus). The different connectivity of fast and slow MNs parallel differences in properties of muscle fibers that they innervate, suggesting that muscle fibers properties, rather than being self‐determined, are the result of differences of their premotor innervation. J. Comp. Neurol. 498:762–785, 2006. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16927266</pmid><doi>10.1002/cne.21092</doi><tpages>24</tpages><orcidid>https://orcid.org/0000-0003-0040-856X</orcidid></addata></record> |
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subjects | Abducens Nerve Abducens Nerve - cytology Abducens Nerve - virology Animals Brain Stem Brain Stem - cytology Brain Stem - virology Eye Movements Female fixation Image Processing, Computer-Assisted Immunohistochemistry Life Sciences Macaca mulatta Motor Neurons Motor Neurons - cytology Motor Neurons - virology Neurons and Cognition Oculomotor Muscles Oculomotor Muscles - innervation Primates Rabies virus saccades smooth pursuit vergence vestibulo-ocular |
title | Horizontal eye movement networks in primates as revealed by retrograde transneuronal transfer of rabies virus: Differences in monosynaptic input to "slow" and "fast" abducens motoneurons |
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