EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding
In early brain development, ascending thalamocortical axons (TCAs) navigate through the ventral telencephalon (VTel) to reach their target regions in the young cerebral cortex. Descending, deep-layer cortical axons subsequently target appropriate thalamic and subcortical target regions. However, pre...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2014-02, Vol.111 (6), p.2188-2193 |
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creator | Robichaux, Michael A. Chenaux, George Ho, Hsin-Yi Henry Soskis, Michael J. Dravis, Christopher Kwan, Kenneth Y. Šestan, Nenad Greenberg, Michael Eldon Henkemeyer, Mark Cowan, Christopher W. |
description | In early brain development, ascending thalamocortical axons (TCAs) navigate through the ventral telencephalon (VTel) to reach their target regions in the young cerebral cortex. Descending, deep-layer cortical axons subsequently target appropriate thalamic and subcortical target regions. However, precisely how and when corticothalamic axons (CTAs) identify their appropriate, reciprocal thalamic targets remains unclear. We show here that EphB1 and EphB2 receptors control proper navigation of a subset of TCA and CTA projections through the VTel. We show in vivo that EphB receptor forward signaling and the ephrinB1 ligand are required during the early navigation of L1-CAM ⁺ thalamic fibers in the VTel, and that the misguided thalamic fibers in EphB1 /2 KO mice appear to interact with cortical subregion-specific axon populations during reciprocal cortical axon guidance. As such, our findings suggest that descending cortical axons identify specific TCA subpopulations in the dorsal VTel to coordinate reciprocal cortical–thalamic connectivity in the early developing brain. |
doi_str_mv | 10.1073/pnas.1324215111 |
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Descending, deep-layer cortical axons subsequently target appropriate thalamic and subcortical target regions. However, precisely how and when corticothalamic axons (CTAs) identify their appropriate, reciprocal thalamic targets remains unclear. We show here that EphB1 and EphB2 receptors control proper navigation of a subset of TCA and CTA projections through the VTel. We show in vivo that EphB receptor forward signaling and the ephrinB1 ligand are required during the early navigation of L1-CAM ⁺ thalamic fibers in the VTel, and that the misguided thalamic fibers in EphB1 /2 KO mice appear to interact with cortical subregion-specific axon populations during reciprocal cortical axon guidance. As such, our findings suggest that descending cortical axons identify specific TCA subpopulations in the dorsal VTel to coordinate reciprocal cortical–thalamic connectivity in the early developing brain.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1324215111</identifier><identifier>PMID: 24453220</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Autistic disorder ; Axons ; Behavioral neuroscience ; Biological Sciences ; Brain ; cerebral cortex ; Cerebral Cortex - metabolism ; Connectivity ; Mice ; Mice, Knockout ; Molecules ; Navigation ; Neurons ; receptor protein-tyrosine kinase ; Receptors ; Receptors, Eph Family - genetics ; Receptors, Eph Family - metabolism ; Rodents ; Signal Transduction ; T cell receptors ; Thalamus ; Thalamus - metabolism</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (6), p.2188-2193</ispartof><rights>copyright © 1993–2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Feb 11, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c622t-88d812e6bbb4cea97dd5636f214f5395b01780f61964830910753d0e82055a403</citedby><cites>FETCH-LOGICAL-c622t-88d812e6bbb4cea97dd5636f214f5395b01780f61964830910753d0e82055a403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/111/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23768838$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23768838$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24453220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Robichaux, Michael A.</creatorcontrib><creatorcontrib>Chenaux, George</creatorcontrib><creatorcontrib>Ho, Hsin-Yi Henry</creatorcontrib><creatorcontrib>Soskis, Michael J.</creatorcontrib><creatorcontrib>Dravis, Christopher</creatorcontrib><creatorcontrib>Kwan, Kenneth Y.</creatorcontrib><creatorcontrib>Šestan, Nenad</creatorcontrib><creatorcontrib>Greenberg, Michael Eldon</creatorcontrib><creatorcontrib>Henkemeyer, Mark</creatorcontrib><creatorcontrib>Cowan, Christopher W.</creatorcontrib><title>EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>In early brain development, ascending thalamocortical axons (TCAs) navigate through the ventral telencephalon (VTel) to reach their target regions in the young cerebral cortex. Descending, deep-layer cortical axons subsequently target appropriate thalamic and subcortical target regions. However, precisely how and when corticothalamic axons (CTAs) identify their appropriate, reciprocal thalamic targets remains unclear. We show here that EphB1 and EphB2 receptors control proper navigation of a subset of TCA and CTA projections through the VTel. We show in vivo that EphB receptor forward signaling and the ephrinB1 ligand are required during the early navigation of L1-CAM ⁺ thalamic fibers in the VTel, and that the misguided thalamic fibers in EphB1 /2 KO mice appear to interact with cortical subregion-specific axon populations during reciprocal cortical axon guidance. As such, our findings suggest that descending cortical axons identify specific TCA subpopulations in the dorsal VTel to coordinate reciprocal cortical–thalamic connectivity in the early developing brain.</description><subject>Animals</subject><subject>Autistic disorder</subject><subject>Axons</subject><subject>Behavioral neuroscience</subject><subject>Biological Sciences</subject><subject>Brain</subject><subject>cerebral cortex</subject><subject>Cerebral Cortex - metabolism</subject><subject>Connectivity</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Molecules</subject><subject>Navigation</subject><subject>Neurons</subject><subject>receptor protein-tyrosine kinase</subject><subject>Receptors</subject><subject>Receptors, Eph Family - genetics</subject><subject>Receptors, Eph Family - metabolism</subject><subject>Rodents</subject><subject>Signal Transduction</subject><subject>T cell receptors</subject><subject>Thalamus</subject><subject>Thalamus - metabolism</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstv1DAQxiMEokvhzAmIxIVL2hm_4lyQoCoPqRIH6NmaJE7Wq2wc7CyP_x5HKdvCpSdL8_3mk2fmy7LnCGcIJT-fRopnyJlgKBHxQbZBqLBQooKH2QaAlYUWTJxkT2LcAUAlNTzOTpgQkjMGm8xdTtv3ebCNnWYf8s6HnxTaPLp-pMGNfZL6w0CzjTkFS0WcbOM61ywtbgq-oSGftzTQPtVobPPGh9ktVfrlx3yiedu5sU1OT7NHHQ3RPrt5T7PrD5ffLj4VV18-fr54d1U0irG50LrVyKyq61o0lqqybaXiqmMoOskrWQOWGjqFlRKap2GhlLwFqxlISQL4afZ29Z0O9d62jR3nQIOZgttT-G08OfOvMrqt6f0PwyumQKtk8ObGIPjvBxtns3exscNAo_WHaFADR14JhfejUggAiVLej4qqQiFBLR94_R-684eQ7rFSaU4tWaLOV6oJPsZgu-OICGYJh1nCYW7DkTpe3t3Mkf-bhjvA0nm0QzTKMNQ6AS9WYBdTWm4NeKmSuuivVr0jb6gPLprrrwxQAaSNgSj5H6EZ0as</recordid><startdate>20140211</startdate><enddate>20140211</enddate><creator>Robichaux, Michael A.</creator><creator>Chenaux, George</creator><creator>Ho, Hsin-Yi Henry</creator><creator>Soskis, Michael J.</creator><creator>Dravis, Christopher</creator><creator>Kwan, Kenneth Y.</creator><creator>Šestan, Nenad</creator><creator>Greenberg, Michael Eldon</creator><creator>Henkemeyer, Mark</creator><creator>Cowan, Christopher W.</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20140211</creationdate><title>EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding</title><author>Robichaux, Michael A. ; Chenaux, George ; Ho, Hsin-Yi Henry ; Soskis, Michael J. ; Dravis, Christopher ; Kwan, Kenneth Y. ; Šestan, Nenad ; Greenberg, Michael Eldon ; Henkemeyer, Mark ; Cowan, Christopher W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c622t-88d812e6bbb4cea97dd5636f214f5395b01780f61964830910753d0e82055a403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Autistic disorder</topic><topic>Axons</topic><topic>Behavioral neuroscience</topic><topic>Biological Sciences</topic><topic>Brain</topic><topic>cerebral cortex</topic><topic>Cerebral Cortex - metabolism</topic><topic>Connectivity</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Molecules</topic><topic>Navigation</topic><topic>Neurons</topic><topic>receptor protein-tyrosine kinase</topic><topic>Receptors</topic><topic>Receptors, Eph Family - genetics</topic><topic>Receptors, Eph Family - metabolism</topic><topic>Rodents</topic><topic>Signal Transduction</topic><topic>T cell receptors</topic><topic>Thalamus</topic><topic>Thalamus - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robichaux, Michael A.</creatorcontrib><creatorcontrib>Chenaux, George</creatorcontrib><creatorcontrib>Ho, Hsin-Yi Henry</creatorcontrib><creatorcontrib>Soskis, Michael J.</creatorcontrib><creatorcontrib>Dravis, Christopher</creatorcontrib><creatorcontrib>Kwan, Kenneth Y.</creatorcontrib><creatorcontrib>Šestan, Nenad</creatorcontrib><creatorcontrib>Greenberg, Michael Eldon</creatorcontrib><creatorcontrib>Henkemeyer, Mark</creatorcontrib><creatorcontrib>Cowan, Christopher W.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robichaux, Michael A.</au><au>Chenaux, George</au><au>Ho, Hsin-Yi Henry</au><au>Soskis, Michael J.</au><au>Dravis, Christopher</au><au>Kwan, Kenneth Y.</au><au>Šestan, Nenad</au><au>Greenberg, Michael Eldon</au><au>Henkemeyer, Mark</au><au>Cowan, Christopher W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2014-02-11</date><risdate>2014</risdate><volume>111</volume><issue>6</issue><spage>2188</spage><epage>2193</epage><pages>2188-2193</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>In early brain development, ascending thalamocortical axons (TCAs) navigate through the ventral telencephalon (VTel) to reach their target regions in the young cerebral cortex. Descending, deep-layer cortical axons subsequently target appropriate thalamic and subcortical target regions. However, precisely how and when corticothalamic axons (CTAs) identify their appropriate, reciprocal thalamic targets remains unclear. We show here that EphB1 and EphB2 receptors control proper navigation of a subset of TCA and CTA projections through the VTel. We show in vivo that EphB receptor forward signaling and the ephrinB1 ligand are required during the early navigation of L1-CAM ⁺ thalamic fibers in the VTel, and that the misguided thalamic fibers in EphB1 /2 KO mice appear to interact with cortical subregion-specific axon populations during reciprocal cortical axon guidance. 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subjects | Animals Autistic disorder Axons Behavioral neuroscience Biological Sciences Brain cerebral cortex Cerebral Cortex - metabolism Connectivity Mice Mice, Knockout Molecules Navigation Neurons receptor protein-tyrosine kinase Receptors Receptors, Eph Family - genetics Receptors, Eph Family - metabolism Rodents Signal Transduction T cell receptors Thalamus Thalamus - metabolism |
title | EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding |
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