Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo
Engrailed transcription factors regulate the expression of guidance cues that pattern retinal axon terminals in the dorsal midbrain. They also act directly to guide axon growth in vitro. We show here that an extracellular En gradient exists in the tectum along the anterior-posterior axis. Neutralizi...
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creator | Wizenmann, Andrea Brunet, Isabelle Lam, Joyce S.Y. Sonnier, Laure Beurdeley, Marine Zarbalis, Konstantinos Weisenhorn-Vogt, Daniela Weinl, Christine Dwivedy, Asha Joliot, Alain Wurst, Wolfgang Holt, Christine Prochiantz, Alain |
description | Engrailed transcription factors regulate the expression of guidance cues that pattern retinal axon terminals in the dorsal midbrain. They also act directly to guide axon growth in vitro. We show here that an extracellular En gradient exists in the tectum along the anterior-posterior axis. Neutralizing extracellular Engrailed in vivo with antibodies expressed in the tectum causes temporal axons to map aberrantly to the posterior tectum in chick and
Xenopus. Furthermore, posterior membranes from wild-type tecta incubated with anti-Engrailed antibodies or posterior membranes from Engrailed-1 knockout mice exhibit diminished repulsive activity for temporal axons. Since EphrinAs play a major role in anterior-posterior mapping, we tested whether Engrailed cooperates with EphrinA5 in vitro. We find that Engrailed restores full repulsion to axons given subthreshold doses of EphrinA5. Collectively, our results indicate that extracellular Engrailed contributes to retinotectal mapping in vivo by modulating the sensitivity of growth cones to EphrinA. |
doi_str_mv | 10.1016/j.neuron.2009.09.018 |
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Xenopus. Furthermore, posterior membranes from wild-type tecta incubated with anti-Engrailed antibodies or posterior membranes from Engrailed-1 knockout mice exhibit diminished repulsive activity for temporal axons. Since EphrinAs play a major role in anterior-posterior mapping, we tested whether Engrailed cooperates with EphrinA5 in vitro. We find that Engrailed restores full repulsion to axons given subthreshold doses of EphrinA5. Collectively, our results indicate that extracellular Engrailed contributes to retinotectal mapping in vivo by modulating the sensitivity of growth cones to EphrinA.</description><identifier>ISSN: 0896-6273</identifier><identifier>EISSN: 1097-4199</identifier><identifier>DOI: 10.1016/j.neuron.2009.09.018</identifier><identifier>PMID: 19914184</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Axons - physiology ; CELLBIO ; Chemotaxis - physiology ; Chick Embryo ; DEVBIO ; Extracellular Space - metabolism ; Glycerol ; Growth Cones - physiology ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; In Vitro Techniques ; Membranes ; Mice ; Mice, Knockout ; MOLNEURO ; Proteins ; Receptors, Eph Family - metabolism ; Retina - embryology ; Retina - growth & development ; Retina - physiology ; Retinal Ganglion Cells - physiology ; RNA polymerase ; Software ; Superior Colliculi - embryology ; Superior Colliculi - growth & development ; Superior Colliculi - physiology ; Visual Pathways - embryology ; Visual Pathways - growth & development ; Visual Pathways - physiology ; Xenopus</subject><ispartof>Neuron (Cambridge, Mass.), 2009-11, Vol.64 (3), p.355-366</ispartof><rights>2009 Elsevier Inc.</rights><rights>Copyright Elsevier Limited Nov 12, 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c587t-187fc188ee4d8d8f0626a6b6e5b5f341769667edc382f77a4236f0ed58e2dfaf3</citedby><cites>FETCH-LOGICAL-c587t-187fc188ee4d8d8f0626a6b6e5b5f341769667edc382f77a4236f0ed58e2dfaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuron.2009.09.018$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19914184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wizenmann, Andrea</creatorcontrib><creatorcontrib>Brunet, Isabelle</creatorcontrib><creatorcontrib>Lam, Joyce S.Y.</creatorcontrib><creatorcontrib>Sonnier, Laure</creatorcontrib><creatorcontrib>Beurdeley, Marine</creatorcontrib><creatorcontrib>Zarbalis, Konstantinos</creatorcontrib><creatorcontrib>Weisenhorn-Vogt, Daniela</creatorcontrib><creatorcontrib>Weinl, Christine</creatorcontrib><creatorcontrib>Dwivedy, Asha</creatorcontrib><creatorcontrib>Joliot, Alain</creatorcontrib><creatorcontrib>Wurst, Wolfgang</creatorcontrib><creatorcontrib>Holt, Christine</creatorcontrib><creatorcontrib>Prochiantz, Alain</creatorcontrib><title>Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo</title><title>Neuron (Cambridge, Mass.)</title><addtitle>Neuron</addtitle><description>Engrailed transcription factors regulate the expression of guidance cues that pattern retinal axon terminals in the dorsal midbrain. They also act directly to guide axon growth in vitro. We show here that an extracellular En gradient exists in the tectum along the anterior-posterior axis. Neutralizing extracellular Engrailed in vivo with antibodies expressed in the tectum causes temporal axons to map aberrantly to the posterior tectum in chick and
Xenopus. Furthermore, posterior membranes from wild-type tecta incubated with anti-Engrailed antibodies or posterior membranes from Engrailed-1 knockout mice exhibit diminished repulsive activity for temporal axons. Since EphrinAs play a major role in anterior-posterior mapping, we tested whether Engrailed cooperates with EphrinA5 in vitro. We find that Engrailed restores full repulsion to axons given subthreshold doses of EphrinA5. Collectively, our results indicate that extracellular Engrailed contributes to retinotectal mapping in vivo by modulating the sensitivity of growth cones to EphrinA.</description><subject>Animals</subject><subject>Axons - physiology</subject><subject>CELLBIO</subject><subject>Chemotaxis - physiology</subject><subject>Chick Embryo</subject><subject>DEVBIO</subject><subject>Extracellular Space - metabolism</subject><subject>Glycerol</subject><subject>Growth Cones - physiology</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>In Vitro Techniques</subject><subject>Membranes</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>MOLNEURO</subject><subject>Proteins</subject><subject>Receptors, Eph Family - metabolism</subject><subject>Retina - embryology</subject><subject>Retina - growth & development</subject><subject>Retina - physiology</subject><subject>Retinal Ganglion Cells - physiology</subject><subject>RNA polymerase</subject><subject>Software</subject><subject>Superior Colliculi - embryology</subject><subject>Superior Colliculi - growth & development</subject><subject>Superior Colliculi - physiology</subject><subject>Visual Pathways - embryology</subject><subject>Visual Pathways - growth & development</subject><subject>Visual Pathways - physiology</subject><subject>Xenopus</subject><issn>0896-6273</issn><issn>1097-4199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kdFrFDEQxoMo9qz-ByIBoT7tmdnNJtkXoZSzLRQUqYJPIbc76eXYS9Zk96j_vVnuaNWHwkAe5jdfZr6PkLfAlsBAfNwuPU4x-GXJWLOcC9QzsgDWyIJD0zwnC6YaUYhSVifkVUpbxoDXDbwkJ7kNHBRfkJ-r-zGaFvt-6k2kK38Xjeuxo19NHF3rBjNios7TcYP0Ngwh94eNa-nl5DrjW6TB0m84Om96en4ffKLXnv5w-_CavLCmT_jm-J6S759XtxdXxc2Xy-uL85uirZUcC1DStqAUIu9UpywTpTBiLbBe17biIEUjhMSurVRppTS8rIRl2NUKy84aW52STwfdYVrvMoc-H9TrIbqdib91ME7_2_Fuo-_CXnPBqqoWWeDDUSCGXxOmUe9cmh0xHsOUtMxbcFbCTJ49SZbA6loAy-D7_8BtmGK2KGmoWSVlA43MFD9QbQwpRbQPSwPTc8Z6qw8Z6zljPReoPPbu74Mfh46hPjqC2fa9w6hT6zBn1bmI7ai74J7-4Q_YzrsT</recordid><startdate>20091112</startdate><enddate>20091112</enddate><creator>Wizenmann, Andrea</creator><creator>Brunet, Isabelle</creator><creator>Lam, Joyce S.Y.</creator><creator>Sonnier, Laure</creator><creator>Beurdeley, Marine</creator><creator>Zarbalis, Konstantinos</creator><creator>Weisenhorn-Vogt, Daniela</creator><creator>Weinl, Christine</creator><creator>Dwivedy, Asha</creator><creator>Joliot, Alain</creator><creator>Wurst, Wolfgang</creator><creator>Holt, Christine</creator><creator>Prochiantz, Alain</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091112</creationdate><title>Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo</title><author>Wizenmann, Andrea ; 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subjects | Animals Axons - physiology CELLBIO Chemotaxis - physiology Chick Embryo DEVBIO Extracellular Space - metabolism Glycerol Growth Cones - physiology Homeodomain Proteins - genetics Homeodomain Proteins - metabolism In Vitro Techniques Membranes Mice Mice, Knockout MOLNEURO Proteins Receptors, Eph Family - metabolism Retina - embryology Retina - growth & development Retina - physiology Retinal Ganglion Cells - physiology RNA polymerase Software Superior Colliculi - embryology Superior Colliculi - growth & development Superior Colliculi - physiology Visual Pathways - embryology Visual Pathways - growth & development Visual Pathways - physiology Xenopus |
title | Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo |
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