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N-syndecan deficiency impairs neural migration in brain

N-syndecan (syndecan-3) is a transmembrane proteoglycan that is abundantly expressed in the major axonal pathways and in the migratory routes of the developing brain. When ligated by heparin-binding (HB) growth-associated molecule (GAM; pleiotrophin), N-syndecan mediates cortactin–Src kinase-depende...

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Autores principales: Hienola, Anni, Tumova, Sarka, Kulesskiy, Evgeny, Rauvala, Heikki
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064262/
https://www.ncbi.nlm.nih.gov/pubmed/16908672
http://dx.doi.org/10.1083/jcb.200602043
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author Hienola, Anni
Tumova, Sarka
Kulesskiy, Evgeny
Rauvala, Heikki
author_facet Hienola, Anni
Tumova, Sarka
Kulesskiy, Evgeny
Rauvala, Heikki
author_sort Hienola, Anni
collection PubMed
description N-syndecan (syndecan-3) is a transmembrane proteoglycan that is abundantly expressed in the major axonal pathways and in the migratory routes of the developing brain. When ligated by heparin-binding (HB) growth-associated molecule (GAM; pleiotrophin), N-syndecan mediates cortactin–Src kinase-dependent neurite outgrowth. However, the functional role of N-syndecan in brain development remains unexplored. In this study, we show that N-syndecan deficiency perturbs the laminar structure of the cerebral cortex as a result of impaired radial migration. In addition, neural migration in the rostral migratory stream is impaired in the N-syndecan–null mice. We suggest that the migration defect depends on impaired HB-GAM–induced Src kinase activation and haptotactic migration. Furthermore, we show that N-syndecan interacts with EGF receptor (EGFR) at the plasma membrane and is required in EGFR-induced neuronal migration.
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spelling pubmed-20642622007-11-29 N-syndecan deficiency impairs neural migration in brain Hienola, Anni Tumova, Sarka Kulesskiy, Evgeny Rauvala, Heikki J Cell Biol Research Articles N-syndecan (syndecan-3) is a transmembrane proteoglycan that is abundantly expressed in the major axonal pathways and in the migratory routes of the developing brain. When ligated by heparin-binding (HB) growth-associated molecule (GAM; pleiotrophin), N-syndecan mediates cortactin–Src kinase-dependent neurite outgrowth. However, the functional role of N-syndecan in brain development remains unexplored. In this study, we show that N-syndecan deficiency perturbs the laminar structure of the cerebral cortex as a result of impaired radial migration. In addition, neural migration in the rostral migratory stream is impaired in the N-syndecan–null mice. We suggest that the migration defect depends on impaired HB-GAM–induced Src kinase activation and haptotactic migration. Furthermore, we show that N-syndecan interacts with EGF receptor (EGFR) at the plasma membrane and is required in EGFR-induced neuronal migration. The Rockefeller University Press 2006-08-14 /pmc/articles/PMC2064262/ /pubmed/16908672 http://dx.doi.org/10.1083/jcb.200602043 Text en Copyright © 2006, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Hienola, Anni
Tumova, Sarka
Kulesskiy, Evgeny
Rauvala, Heikki
N-syndecan deficiency impairs neural migration in brain
title N-syndecan deficiency impairs neural migration in brain
title_full N-syndecan deficiency impairs neural migration in brain
title_fullStr N-syndecan deficiency impairs neural migration in brain
title_full_unstemmed N-syndecan deficiency impairs neural migration in brain
title_short N-syndecan deficiency impairs neural migration in brain
title_sort n-syndecan deficiency impairs neural migration in brain
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064262/
https://www.ncbi.nlm.nih.gov/pubmed/16908672
http://dx.doi.org/10.1083/jcb.200602043
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