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Afferent Connectivity of the Zebrafish Habenulae
The habenulae are bilateral nuclei located in the dorsal diencephalon that are conserved across vertebrates. Here we describe the main afferents to the habenulae in larval and adult zebrafish. We observe afferents from the subpallium, nucleus rostrolateralis, posterior tuberculum, posterior hypothal...
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Published in: | Frontiers in neural circuits 2016-04, Vol.10, p.30-30 |
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description | The habenulae are bilateral nuclei located in the dorsal diencephalon that are conserved across vertebrates. Here we describe the main afferents to the habenulae in larval and adult zebrafish. We observe afferents from the subpallium, nucleus rostrolateralis, posterior tuberculum, posterior hypothalamic lobe, median raphe; we also see asymmetric afferents from olfactory bulb to the right habenula, and from the parapineal to the left habenula. In addition, we find afferents from a ventrolateral telencephalic nucleus that neurochemical and hodological data identify as the ventral entopeduncular nucleus (vENT), confirming and extending observations of Amo et al. (2014). Fate map and marker studies suggest that vENT originates from the diencephalic prethalamic eminence and extends into the lateral telencephalon from 48 to 120 hour post-fertilization (hpf). No afferents to the habenula were observed from the dorsal entopeduncular nucleus (dENT). Consequently, we confirm that the vENT (and not the dENT) should be considered as the entopeduncular nucleus "proper" in zebrafish. Furthermore, comparison with data in other vertebrates suggests that the vENT is a conserved basal ganglia nucleus, being homologous to the entopeduncular nucleus of mammals (internal segment of the globus pallidus of primates) by both embryonic origin and projections, as previously suggested by Amo et al. (2014). |
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Here we describe the main afferents to the habenulae in larval and adult zebrafish. We observe afferents from the subpallium, nucleus rostrolateralis, posterior tuberculum, posterior hypothalamic lobe, median raphe; we also see asymmetric afferents from olfactory bulb to the right habenula, and from the parapineal to the left habenula. In addition, we find afferents from a ventrolateral telencephalic nucleus that neurochemical and hodological data identify as the ventral entopeduncular nucleus (vENT), confirming and extending observations of Amo et al. (2014). Fate map and marker studies suggest that vENT originates from the diencephalic prethalamic eminence and extends into the lateral telencephalon from 48 to 120 hour post-fertilization (hpf). No afferents to the habenula were observed from the dorsal entopeduncular nucleus (dENT). Consequently, we confirm that the vENT (and not the dENT) should be considered as the entopeduncular nucleus "proper" in zebrafish. Furthermore, comparison with data in other vertebrates suggests that the vENT is a conserved basal ganglia nucleus, being homologous to the entopeduncular nucleus of mammals (internal segment of the globus pallidus of primates) by both embryonic origin and projections, as previously suggested by Amo et al. 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This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2016 Turner, Hawkins, Yáñez, Anadón, Wilson and Folgueira. 2016 Turner, Hawkins, Yáñez, Anadón, Wilson and Folgueira</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-370d2a67d122d69c2fcf9473fb2ec544fbd21e1dbc1e019cbd122484ecfc842a3</citedby><cites>FETCH-LOGICAL-c490t-370d2a67d122d69c2fcf9473fb2ec544fbd21e1dbc1e019cbd122484ecfc842a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2296243489/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2296243489?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27199671$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Turner, Katherine J</creatorcontrib><creatorcontrib>Hawkins, Thomas A</creatorcontrib><creatorcontrib>Yáñez, Julián</creatorcontrib><creatorcontrib>Anadón, Ramón</creatorcontrib><creatorcontrib>Wilson, Stephen W</creatorcontrib><creatorcontrib>Folgueira, Mónica</creatorcontrib><title>Afferent Connectivity of the Zebrafish Habenulae</title><title>Frontiers in neural circuits</title><addtitle>Front Neural Circuits</addtitle><description>The habenulae are bilateral nuclei located in the dorsal diencephalon that are conserved across vertebrates. Here we describe the main afferents to the habenulae in larval and adult zebrafish. We observe afferents from the subpallium, nucleus rostrolateralis, posterior tuberculum, posterior hypothalamic lobe, median raphe; we also see asymmetric afferents from olfactory bulb to the right habenula, and from the parapineal to the left habenula. In addition, we find afferents from a ventrolateral telencephalic nucleus that neurochemical and hodological data identify as the ventral entopeduncular nucleus (vENT), confirming and extending observations of Amo et al. (2014). Fate map and marker studies suggest that vENT originates from the diencephalic prethalamic eminence and extends into the lateral telencephalon from 48 to 120 hour post-fertilization (hpf). No afferents to the habenula were observed from the dorsal entopeduncular nucleus (dENT). Consequently, we confirm that the vENT (and not the dENT) should be considered as the entopeduncular nucleus "proper" in zebrafish. Furthermore, comparison with data in other vertebrates suggests that the vENT is a conserved basal ganglia nucleus, being homologous to the entopeduncular nucleus of mammals (internal segment of the globus pallidus of primates) by both embryonic origin and projections, as previously suggested by Amo et al. (2014).</description><subject>Afferent Pathways - physiology</subject><subject>afferents</subject><subject>Amino Acids - metabolism</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Asymmetry</subject><subject>Basal Ganglia</subject><subject>Biology</subject><subject>Brain</subject><subject>Brain Mapping</subject><subject>Calbindin 2 - genetics</subject><subject>Calbindin 2 - metabolism</subject><subject>connections</subject><subject>Connectivity</subject><subject>Danio rerio</subject><subject>Diencephalon</subject><subject>Embryo, Nonmammalian</subject><subject>Embryos</subject><subject>Entopeduncular Nucleus</subject><subject>Functional Laterality</subject><subject>Gene Expression Regulation, Developmental - genetics</subject><subject>Gene Expression Regulation, Developmental - physiology</subject><subject>Globus pallidus</subject><subject>Glutamic Acid - metabolism</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Habenula</subject><subject>Habenula - cytology</subject><subject>Habenula - growth & development</subject><subject>Habenula - physiology</subject><subject>Hypothalamus</subject><subject>Larva</subject><subject>Mammals</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neural networks</subject><subject>Neurons - metabolism</subject><subject>Neuroscience</subject><subject>Olfactory Bulb</subject><subject>Sensory neurons</subject><subject>Telencephalon</subject><subject>University colleges</subject><subject>Vertebrates</subject><subject>Zebrafish</subject><subject>Zebrafish Proteins - genetics</subject><subject>Zebrafish Proteins - metabolism</subject><issn>1662-5110</issn><issn>1662-5110</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkctrGzEQh0VpaFy3957KQi-92B09Vru6FIJJ64Chl-SSi9BqR7HMepVKuwb_95EfCUlOen3zMaMfId8ozDmv1S_XWx_nDKicAwCHD2RCpWSzklL4-Gp_ST6ntAGQTJbiE7lkFVVKVnRC4Mo5jNgPxSL0PdrB7_ywL4IrhjUW99hE43xaF0vTYD92Br-QC2e6hF_P65Tc_bm-XSxnq39_bxZXq5kVCoYZr6BlRlYtZayVyjJnnRIVdw1DWwrhmpZRpG1jKQJVtjmAohZona0FM3xKbk7eNpiNfox-a-JeB-P18SLEB23i4G2H2oBCSUsHShqBpTL5mDWSurZxdeWy6_fJ9Tg2W2xtHjea7o307Uvv1_oh7HRuSCjGs-DnWRDD_xHToLc-Wew602MYk6aVAlFyxSCjP96hmzDGPn-VZkxJJrioVabgRNkYUoroXpqhoA_R6mO0-hCtPkabS76_HuKl4DlL_gROY6BF</recordid><startdate>20160426</startdate><enddate>20160426</enddate><creator>Turner, Katherine J</creator><creator>Hawkins, Thomas A</creator><creator>Yáñez, Julián</creator><creator>Anadón, Ramón</creator><creator>Wilson, Stephen W</creator><creator>Folgueira, Mónica</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><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>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160426</creationdate><title>Afferent Connectivity of the Zebrafish Habenulae</title><author>Turner, Katherine J ; Hawkins, Thomas A ; Yáñez, Julián ; Anadón, Ramón ; Wilson, Stephen W ; Folgueira, Mónica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-370d2a67d122d69c2fcf9473fb2ec544fbd21e1dbc1e019cbd122484ecfc842a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Afferent Pathways - physiology</topic><topic>afferents</topic><topic>Amino Acids - metabolism</topic><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Asymmetry</topic><topic>Basal Ganglia</topic><topic>Biology</topic><topic>Brain</topic><topic>Brain Mapping</topic><topic>Calbindin 2 - genetics</topic><topic>Calbindin 2 - metabolism</topic><topic>connections</topic><topic>Connectivity</topic><topic>Danio rerio</topic><topic>Diencephalon</topic><topic>Embryo, Nonmammalian</topic><topic>Embryos</topic><topic>Entopeduncular Nucleus</topic><topic>Functional Laterality</topic><topic>Gene Expression Regulation, Developmental - genetics</topic><topic>Gene Expression Regulation, Developmental - physiology</topic><topic>Globus pallidus</topic><topic>Glutamic Acid - metabolism</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Habenula</topic><topic>Habenula - cytology</topic><topic>Habenula - growth & development</topic><topic>Habenula - physiology</topic><topic>Hypothalamus</topic><topic>Larva</topic><topic>Mammals</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neural networks</topic><topic>Neurons - metabolism</topic><topic>Neuroscience</topic><topic>Olfactory Bulb</topic><topic>Sensory neurons</topic><topic>Telencephalon</topic><topic>University colleges</topic><topic>Vertebrates</topic><topic>Zebrafish</topic><topic>Zebrafish Proteins - genetics</topic><topic>Zebrafish Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Turner, Katherine J</creatorcontrib><creatorcontrib>Hawkins, Thomas A</creatorcontrib><creatorcontrib>Yáñez, Julián</creatorcontrib><creatorcontrib>Anadón, Ramón</creatorcontrib><creatorcontrib>Wilson, Stephen W</creatorcontrib><creatorcontrib>Folgueira, Mónica</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in neural circuits</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Turner, Katherine J</au><au>Hawkins, Thomas A</au><au>Yáñez, Julián</au><au>Anadón, Ramón</au><au>Wilson, Stephen W</au><au>Folgueira, Mónica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Afferent Connectivity of the Zebrafish Habenulae</atitle><jtitle>Frontiers in neural circuits</jtitle><addtitle>Front Neural Circuits</addtitle><date>2016-04-26</date><risdate>2016</risdate><volume>10</volume><spage>30</spage><epage>30</epage><pages>30-30</pages><issn>1662-5110</issn><eissn>1662-5110</eissn><abstract>The habenulae are bilateral nuclei located in the dorsal diencephalon that are conserved across vertebrates. Here we describe the main afferents to the habenulae in larval and adult zebrafish. We observe afferents from the subpallium, nucleus rostrolateralis, posterior tuberculum, posterior hypothalamic lobe, median raphe; we also see asymmetric afferents from olfactory bulb to the right habenula, and from the parapineal to the left habenula. In addition, we find afferents from a ventrolateral telencephalic nucleus that neurochemical and hodological data identify as the ventral entopeduncular nucleus (vENT), confirming and extending observations of Amo et al. (2014). Fate map and marker studies suggest that vENT originates from the diencephalic prethalamic eminence and extends into the lateral telencephalon from 48 to 120 hour post-fertilization (hpf). No afferents to the habenula were observed from the dorsal entopeduncular nucleus (dENT). Consequently, we confirm that the vENT (and not the dENT) should be considered as the entopeduncular nucleus "proper" in zebrafish. Furthermore, comparison with data in other vertebrates suggests that the vENT is a conserved basal ganglia nucleus, being homologous to the entopeduncular nucleus of mammals (internal segment of the globus pallidus of primates) by both embryonic origin and projections, as previously suggested by Amo et al. (2014).</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>27199671</pmid><doi>10.3389/fncir.2016.00030</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Afferent Pathways - physiology afferents Amino Acids - metabolism Animals Animals, Genetically Modified Asymmetry Basal Ganglia Biology Brain Brain Mapping Calbindin 2 - genetics Calbindin 2 - metabolism connections Connectivity Danio rerio Diencephalon Embryo, Nonmammalian Embryos Entopeduncular Nucleus Functional Laterality Gene Expression Regulation, Developmental - genetics Gene Expression Regulation, Developmental - physiology Globus pallidus Glutamic Acid - metabolism Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Habenula Habenula - cytology Habenula - growth & development Habenula - physiology Hypothalamus Larva Mammals Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Neural networks Neurons - metabolism Neuroscience Olfactory Bulb Sensory neurons Telencephalon University colleges Vertebrates Zebrafish Zebrafish Proteins - genetics Zebrafish Proteins - metabolism |
title | Afferent Connectivity of the Zebrafish Habenulae |
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