Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1
Oligodendrocytes, the myelin-forming cells of the CNS, are generated from multiple foci distributed along the developing neural tube. Little is known about the endogenous guidance cues controlling the migration of oligodendrocyte precursor cells (OPCs) from their site of emergence toward their final...
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description | Oligodendrocytes, the myelin-forming cells of the CNS, are generated from multiple foci distributed along the developing neural tube. Little is known about the endogenous guidance cues controlling the migration of oligodendrocyte precursor cells (OPCs) from their site of emergence toward their final destination, mainly the future white matter tracts. During embryonic development, the optic nerve is populated by OPCs originating in the diencephalon that migrate from the chiasm toward the retina. Here we show that OPCs migrating into the embryonic optic nerve express the semaphorin receptors neuropilin-1 and -2, as well as deleted in colorectal cancer (DCC) and, to a lesser extend unc5H1, two of the netrin-1 receptors. Using a functional migration assay, we provide evidence that Sema 3A and netrin-1 exert opposite chemotactic effects, repulsive or attractive, respectively, on embryonic OPCs. In addition, we show that Sema 3F has a dual effect, chemoattractive and mitogenic on embryonic OPCs. The localization of cells expressing Sema 3A, Sema 3F, and netrin-1 is consistent with a role for these ligands in the migration of OPCs in the embryonic optic nerve. Altogether, our results suggest that the migration of OPCs in the embryonic optic nerve is modulated by a balance of effects mediated by members of the semaphorin and netrin families. |
doi_str_mv | 10.1523/jneurosci.22-14-05992.2002 |
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Little is known about the endogenous guidance cues controlling the migration of oligodendrocyte precursor cells (OPCs) from their site of emergence toward their final destination, mainly the future white matter tracts. During embryonic development, the optic nerve is populated by OPCs originating in the diencephalon that migrate from the chiasm toward the retina. Here we show that OPCs migrating into the embryonic optic nerve express the semaphorin receptors neuropilin-1 and -2, as well as deleted in colorectal cancer (DCC) and, to a lesser extend unc5H1, two of the netrin-1 receptors. Using a functional migration assay, we provide evidence that Sema 3A and netrin-1 exert opposite chemotactic effects, repulsive or attractive, respectively, on embryonic OPCs. In addition, we show that Sema 3F has a dual effect, chemoattractive and mitogenic on embryonic OPCs. The localization of cells expressing Sema 3A, Sema 3F, and netrin-1 is consistent with a role for these ligands in the migration of OPCs in the embryonic optic nerve. Altogether, our results suggest that the migration of OPCs in the embryonic optic nerve is modulated by a balance of effects mediated by members of the semaphorin and netrin families.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.22-14-05992.2002</identifier><identifier>PMID: 12122061</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Animals ; Cell Adhesion Molecules - biosynthesis ; Cell Division - drug effects ; Cell Division - physiology ; Cell Line ; Cell Lineage ; Cell Movement - drug effects ; Cell Movement - physiology ; Chemotaxis - drug effects ; Chemotaxis - physiology ; Culture Techniques ; DCC Receptor ; Glycoproteins - metabolism ; Glycoproteins - pharmacology ; Humans ; Life Sciences ; Membrane Proteins - metabolism ; Membrane Proteins - pharmacology ; Mice ; Nerve Growth Factors - metabolism ; Nerve Growth Factors - pharmacology ; Nerve Tissue Proteins - biosynthesis ; Nerve Tissue Proteins - metabolism ; Nerve Tissue Proteins - pharmacology ; Netrin Receptors ; Netrin-1 ; Neurons and Cognition ; Neuropilin-1 ; Oligodendroglia - cytology ; Oligodendroglia - drug effects ; Oligodendroglia - metabolism ; Optic Nerve - cytology ; Optic Nerve - embryology ; Optic Nerve - metabolism ; Receptors, Cell Surface - biosynthesis ; Semaphorin-3A ; Stem Cells - cytology ; Stem Cells - drug effects ; Stem Cells - metabolism ; Tumor Suppressor Proteins - biosynthesis</subject><ispartof>The Journal of neuroscience, 2002-07, Vol.22 (14), p.5992-6004</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2002 Society for Neuroscience 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c642t-c6b97a5f06766a52c6df0961648ced4f6b7d94712042bde598dcc1a7f8476bf43</citedby><cites>FETCH-LOGICAL-c642t-c6b97a5f06766a52c6df0961648ced4f6b7d94712042bde598dcc1a7f8476bf43</cites><orcidid>0000-0003-3397-0292 ; 0000-0001-7577-3794</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757938/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757938/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12122061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-01936468$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Spassky, Nathalie</creatorcontrib><creatorcontrib>de Castro, Fernando</creatorcontrib><creatorcontrib>Le Bras, Barbara</creatorcontrib><creatorcontrib>Heydon, Katharina</creatorcontrib><creatorcontrib>Queraud-LeSaux, Francoise</creatorcontrib><creatorcontrib>Bloch-Gallego, Evelyne</creatorcontrib><creatorcontrib>Chedotal, Alain</creatorcontrib><creatorcontrib>Zalc, Bernard</creatorcontrib><creatorcontrib>Thomas, Jean-Leon</creatorcontrib><title>Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Oligodendrocytes, the myelin-forming cells of the CNS, are generated from multiple foci distributed along the developing neural tube. Little is known about the endogenous guidance cues controlling the migration of oligodendrocyte precursor cells (OPCs) from their site of emergence toward their final destination, mainly the future white matter tracts. During embryonic development, the optic nerve is populated by OPCs originating in the diencephalon that migrate from the chiasm toward the retina. Here we show that OPCs migrating into the embryonic optic nerve express the semaphorin receptors neuropilin-1 and -2, as well as deleted in colorectal cancer (DCC) and, to a lesser extend unc5H1, two of the netrin-1 receptors. Using a functional migration assay, we provide evidence that Sema 3A and netrin-1 exert opposite chemotactic effects, repulsive or attractive, respectively, on embryonic OPCs. In addition, we show that Sema 3F has a dual effect, chemoattractive and mitogenic on embryonic OPCs. The localization of cells expressing Sema 3A, Sema 3F, and netrin-1 is consistent with a role for these ligands in the migration of OPCs in the embryonic optic nerve. Altogether, our results suggest that the migration of OPCs in the embryonic optic nerve is modulated by a balance of effects mediated by members of the semaphorin and netrin families.</description><subject>Animals</subject><subject>Cell Adhesion Molecules - biosynthesis</subject><subject>Cell Division - drug effects</subject><subject>Cell Division - physiology</subject><subject>Cell Line</subject><subject>Cell Lineage</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - physiology</subject><subject>Chemotaxis - drug effects</subject><subject>Chemotaxis - physiology</subject><subject>Culture Techniques</subject><subject>DCC Receptor</subject><subject>Glycoproteins - metabolism</subject><subject>Glycoproteins - pharmacology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Membrane Proteins - metabolism</subject><subject>Membrane Proteins - pharmacology</subject><subject>Mice</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Nerve Growth Factors - pharmacology</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Nerve Tissue Proteins - pharmacology</subject><subject>Netrin Receptors</subject><subject>Netrin-1</subject><subject>Neurons and Cognition</subject><subject>Neuropilin-1</subject><subject>Oligodendroglia - cytology</subject><subject>Oligodendroglia - drug effects</subject><subject>Oligodendroglia - metabolism</subject><subject>Optic Nerve - cytology</subject><subject>Optic Nerve - embryology</subject><subject>Optic Nerve - metabolism</subject><subject>Receptors, Cell Surface - biosynthesis</subject><subject>Semaphorin-3A</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - drug effects</subject><subject>Stem Cells - metabolism</subject><subject>Tumor Suppressor Proteins - biosynthesis</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1v0zAUhiMEYt3gL6CICxAXKT6OY8dcTJrK2IbKKjHGreXYTurJiYvdrNq_n0Mrvm64sS2f5zz20ZtlrwHNocLl-7vBjMFHZecYF0AKVHGO5xgh_CSbJYIXmCB4ms0QZqighJGj7DjGO4QQQ8CeZ0eAAWNEYZZ9_2iDUVvrB-nyi9FqOSiT-zZfOdt5bQYdfOdsKn6xXZATmDcP-cLJGPMyvzG93Kx9sEPM5aDza7NN5wJeZM9a6aJ5edhPsttP598Wl8VydXG1OFsWihK8TWvDmaxaRBmlssKK6hZxCpTUymjS0oZpThhgRHCjTcVrrRRI1taE0aYl5Ul2uvduxqY3WplhG6QTm2B7GR6El1b8XRnsWnT-XlBWMV7WSfBuL1j_03Z5thTTHQJeUkLre0jsm8Njwf8YTdyK3kZlnJOD8WMUDDig5P0vCDUrAdUogR_2oEp5xmDaX18AJKasxefr89uvq5vFlcBYABE_sxZT1qn51Z-z_249hJuAt4fZbLfepZxF7KVzCQex2-32wslXPgJQALUF</recordid><startdate>20020715</startdate><enddate>20020715</enddate><creator>Spassky, Nathalie</creator><creator>de Castro, Fernando</creator><creator>Le Bras, Barbara</creator><creator>Heydon, Katharina</creator><creator>Queraud-LeSaux, Francoise</creator><creator>Bloch-Gallego, Evelyne</creator><creator>Chedotal, Alain</creator><creator>Zalc, Bernard</creator><creator>Thomas, Jean-Leon</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</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>7TK</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3397-0292</orcidid><orcidid>https://orcid.org/0000-0001-7577-3794</orcidid></search><sort><creationdate>20020715</creationdate><title>Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1</title><author>Spassky, Nathalie ; de Castro, Fernando ; Le Bras, Barbara ; Heydon, Katharina ; Queraud-LeSaux, Francoise ; Bloch-Gallego, Evelyne ; Chedotal, Alain ; Zalc, Bernard ; Thomas, Jean-Leon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c642t-c6b97a5f06766a52c6df0961648ced4f6b7d94712042bde598dcc1a7f8476bf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Cell Adhesion Molecules - biosynthesis</topic><topic>Cell Division - drug effects</topic><topic>Cell Division - physiology</topic><topic>Cell Line</topic><topic>Cell Lineage</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - physiology</topic><topic>Chemotaxis - drug effects</topic><topic>Chemotaxis - physiology</topic><topic>Culture Techniques</topic><topic>DCC Receptor</topic><topic>Glycoproteins - metabolism</topic><topic>Glycoproteins - pharmacology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Membrane Proteins - metabolism</topic><topic>Membrane Proteins - pharmacology</topic><topic>Mice</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Nerve Growth Factors - pharmacology</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Nerve Tissue Proteins - pharmacology</topic><topic>Netrin Receptors</topic><topic>Netrin-1</topic><topic>Neurons and Cognition</topic><topic>Neuropilin-1</topic><topic>Oligodendroglia - cytology</topic><topic>Oligodendroglia - drug effects</topic><topic>Oligodendroglia - metabolism</topic><topic>Optic Nerve - cytology</topic><topic>Optic Nerve - embryology</topic><topic>Optic Nerve - metabolism</topic><topic>Receptors, Cell Surface - biosynthesis</topic><topic>Semaphorin-3A</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - drug effects</topic><topic>Stem Cells - metabolism</topic><topic>Tumor Suppressor Proteins - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spassky, Nathalie</creatorcontrib><creatorcontrib>de Castro, Fernando</creatorcontrib><creatorcontrib>Le Bras, Barbara</creatorcontrib><creatorcontrib>Heydon, Katharina</creatorcontrib><creatorcontrib>Queraud-LeSaux, Francoise</creatorcontrib><creatorcontrib>Bloch-Gallego, Evelyne</creatorcontrib><creatorcontrib>Chedotal, Alain</creatorcontrib><creatorcontrib>Zalc, Bernard</creatorcontrib><creatorcontrib>Thomas, Jean-Leon</creatorcontrib><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><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spassky, Nathalie</au><au>de Castro, Fernando</au><au>Le Bras, Barbara</au><au>Heydon, Katharina</au><au>Queraud-LeSaux, Francoise</au><au>Bloch-Gallego, Evelyne</au><au>Chedotal, Alain</au><au>Zalc, Bernard</au><au>Thomas, Jean-Leon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2002-07-15</date><risdate>2002</risdate><volume>22</volume><issue>14</issue><spage>5992</spage><epage>6004</epage><pages>5992-6004</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Oligodendrocytes, the myelin-forming cells of the CNS, are generated from multiple foci distributed along the developing neural tube. Little is known about the endogenous guidance cues controlling the migration of oligodendrocyte precursor cells (OPCs) from their site of emergence toward their final destination, mainly the future white matter tracts. During embryonic development, the optic nerve is populated by OPCs originating in the diencephalon that migrate from the chiasm toward the retina. Here we show that OPCs migrating into the embryonic optic nerve express the semaphorin receptors neuropilin-1 and -2, as well as deleted in colorectal cancer (DCC) and, to a lesser extend unc5H1, two of the netrin-1 receptors. Using a functional migration assay, we provide evidence that Sema 3A and netrin-1 exert opposite chemotactic effects, repulsive or attractive, respectively, on embryonic OPCs. In addition, we show that Sema 3F has a dual effect, chemoattractive and mitogenic on embryonic OPCs. The localization of cells expressing Sema 3A, Sema 3F, and netrin-1 is consistent with a role for these ligands in the migration of OPCs in the embryonic optic nerve. Altogether, our results suggest that the migration of OPCs in the embryonic optic nerve is modulated by a balance of effects mediated by members of the semaphorin and netrin families.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>12122061</pmid><doi>10.1523/jneurosci.22-14-05992.2002</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-3397-0292</orcidid><orcidid>https://orcid.org/0000-0001-7577-3794</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Adhesion Molecules - biosynthesis Cell Division - drug effects Cell Division - physiology Cell Line Cell Lineage Cell Movement - drug effects Cell Movement - physiology Chemotaxis - drug effects Chemotaxis - physiology Culture Techniques DCC Receptor Glycoproteins - metabolism Glycoproteins - pharmacology Humans Life Sciences Membrane Proteins - metabolism Membrane Proteins - pharmacology Mice Nerve Growth Factors - metabolism Nerve Growth Factors - pharmacology Nerve Tissue Proteins - biosynthesis Nerve Tissue Proteins - metabolism Nerve Tissue Proteins - pharmacology Netrin Receptors Netrin-1 Neurons and Cognition Neuropilin-1 Oligodendroglia - cytology Oligodendroglia - drug effects Oligodendroglia - metabolism Optic Nerve - cytology Optic Nerve - embryology Optic Nerve - metabolism Receptors, Cell Surface - biosynthesis Semaphorin-3A Stem Cells - cytology Stem Cells - drug effects Stem Cells - metabolism Tumor Suppressor Proteins - biosynthesis |
title | Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1 |
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