FAK-MAPK-dependent adhesion disassembly downstream of L1 contributes to semaphorin3A-induced collapse

Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin‐As signalling coreceptors. In the developing cerebral cortex, the Ig superfamily cell adhesion molecule L1 associates with Nrp1. Intriguingly, the genetic removal of L1 blocks axon responses of cor...

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Published inThe EMBO journal Vol. 27; no. 11; pp. 1549 - 1562
Main Authors Bechara, Ahmad, Nawabi, Homaira, Moret, Frédéric, Yaron, Avraham, Weaver, Eli, Bozon, Muriel, Abouzid, Karima, Guan, Jun-Lin, Tessier-Lavigne, Marc, Lemmon, Vance, Castellani, Valérie
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 04.06.2008
Blackwell Publishing Ltd
EMBO Press
Nature Publishing Group
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Abstract Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin‐As signalling coreceptors. In the developing cerebral cortex, the Ig superfamily cell adhesion molecule L1 associates with Nrp1. Intriguingly, the genetic removal of L1 blocks axon responses of cortical neurons to Sema3A in vitro despite the expression of Plexin‐As in the cortex, suggesting either that L1 substitutes for Plexin‐As or that L1 and Plexin‐A are both required and mediate distinct roles. We report that association of Nrp1 with L1 but not Plexin‐As mediates the recruitment and activation of a Sema3A‐induced focal adhesion kinase–mitogen‐activated protein kinase cascade. This signalling downstream of L1 is needed for the disassembly of adherent points formed in growth cones and subsequently their collapse response to Sema3A. Plexin‐As and L1 are coexpressed and present in common complexes in cortical neurons and both dominant‐negative forms of Plexin‐A and L1 impair their response to Sema3A. Consistently, Nrp1‐expressing cortical projections are defective in mice lacking Plexin‐A3, Plexin‐A4 or L1. This reveals that specific signalling activities downstream of L1 and Plexin‐As cooperate for mediating the axon guidance effects of Sema3A.
AbstractList Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin‐As signalling coreceptors. In the developing cerebral cortex, the Ig superfamily cell adhesion molecule L1 associates with Nrp1. Intriguingly, the genetic removal of L1 blocks axon responses of cortical neurons to Sema3A in vitro despite the expression of Plexin‐As in the cortex, suggesting either that L1 substitutes for Plexin‐As or that L1 and Plexin‐A are both required and mediate distinct roles. We report that association of Nrp1 with L1 but not Plexin‐As mediates the recruitment and activation of a Sema3A‐induced focal adhesion kinase–mitogen‐activated protein kinase cascade. This signalling downstream of L1 is needed for the disassembly of adherent points formed in growth cones and subsequently their collapse response to Sema3A. Plexin‐As and L1 are coexpressed and present in common complexes in cortical neurons and both dominant‐negative forms of Plexin‐A and L1 impair their response to Sema3A. Consistently, Nrp1‐expressing cortical projections are defective in mice lacking Plexin‐A3, Plexin‐A4 or L1. This reveals that specific signalling activities downstream of L1 and Plexin‐As cooperate for mediating the axon guidance effects of Sema3A.
Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin-As signalling coreceptors. In the developing cerebral cortex, the Ig superfamily cell adhesion molecule L1 associates with Nrp1. Intriguingly, the genetic removal of L1 blocks axon responses of cortical neurons to Sema3A in vitro despite the expression of Plexin-As in the cortex, suggesting either that L1 substitutes for Plexin-As or that L1 and Plexin-A are both required and mediate distinct roles. We report that association of Nrp1 with L1 but not Plexin-As mediates the recruitment and activation of a Sema3A-induced focal adhesion kinase-mitogen-activated protein kinase cascade. This signalling downstream of L1 is needed for the disassembly of adherent points formed in growth cones and subsequently their collapse response to Sema3A. Plexin-As and L1 are coexpressed and present in common complexes in cortical neurons and both dominant-negative forms of Plexin-A and L1 impair their response to Sema3A. Consistently, Nrp1-expressing cortical projections are defective in mice lacking Plexin-A3, Plexin-A4 or L1. This reveals that specific signalling activities downstream of L1 and Plexin-As cooperate for mediating the axon guidance effects of Sema3A. [PUBLICATION ABSTRACT]
Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin-As signalling coreceptors. In the developing cerebral cortex, the Ig superfamily cell adhesion molecule L1 associates with Nrp1. Intriguingly, the genetic removal of L1 blocks axon responses of cortical neurons to Sema3A in vitro despite the expression of Plexin-As in the cortex, suggesting either that L1 substitutes for Plexin-As or that L1 and Plexin-A are both required and mediate distinct roles. We report that association of Nrp1 with L1 but not Plexin-As mediates the recruitment and activation of a Sema3A-induced focal adhesion kinase–mitogen-activated protein kinase cascade. This signalling downstream of L1 is needed for the disassembly of adherent points formed in growth cones and subsequently their collapse response to Sema3A. Plexin-As and L1 are coexpressed and present in common complexes in cortical neurons and both dominant-negative forms of Plexin-A and L1 impair their response to Sema3A. Consistently, Nrp1-expressing cortical projections are defective in mice lacking Plexin-A3, Plexin-A4 or L1. This reveals that specific signalling activities downstream of L1 and Plexin-As cooperate for mediating the axon guidance effects of Sema3A.
Author Bechara, Ahmad
Yaron, Avraham
Tessier-Lavigne, Marc
Guan, Jun-Lin
Bozon, Muriel
Moret, Frédéric
Weaver, Eli
Castellani, Valérie
Abouzid, Karima
Lemmon, Vance
Nawabi, Homaira
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  organization: The Miami Project to Cure Paralysis, University of Miami, FL, Miami, USA
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  organization: Cornell University, NY, Ithaca, USA
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  email: castellani@cgmc.univ-lyon1.fr
  organization: Université de Lyon, Centre de Génétique Moléculaire et Cellulaire (CGMC) UMR CNRS 5534, Villeurbanne, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/18464795$$D View this record in MEDLINE/PubMed
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Copyright Nature Publishing Group Jun 4, 2008
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Thelen K (emboj200886-b40) 2002; 15
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Garrity PA (emboj200886-b18) 2005; 8
Kamiguchi H (emboj200886-b24) 2000; 12
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Carter N (emboj200886-b4) 2002; 4
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Woo S (emboj200886-b45) 2006; 26
Crowley E (emboj200886-b14) 1995; 131
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Snippet Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin‐As signalling coreceptors. In the developing cerebral...
Axonal receptors for class 3 semaphorins (Sema3s) are heterocomplexes of neuropilins (Nrps) and Plexin-As signalling coreceptors. In the developing cerebral...
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StartPage 1549
SubjectTerms Adhesion
Animals
axon guidance
Axons
Axons - metabolism
Biochemistry
Cell Adhesion
Cell adhesion & migration
Cellular Biology
Cerebral Cortex
Cerebral Cortex - cytology
Cerebral Cortex - growth & development
Cerebral Cortex - metabolism
focal adhesion
Focal Adhesion Protein-Tyrosine Kinases
Focal Adhesion Protein-Tyrosine Kinases - metabolism
Genetics
Growth Cones
Growth Cones - metabolism
Life Sciences
Mice
Mice, Mutant Strains
Mitogen-Activated Protein Kinase 1
Mitogen-Activated Protein Kinase 1 - metabolism
Mitogen-Activated Protein Kinase 3
Mitogen-Activated Protein Kinase 3 - metabolism
Molecular biology
Nerve Tissue Proteins
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Neural Cell Adhesion Molecule L1
Neural Cell Adhesion Molecule L1 - genetics
Neural Cell Adhesion Molecule L1 - metabolism
Neuropilin-1
Neuropilin-1 - metabolism
receptor
Receptors, Cell Surface
Receptors, Cell Surface - genetics
Receptors, Cell Surface - metabolism
Semaphorin-3A
Semaphorin-3A - metabolism
semaphorins
Signal Transduction
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Title FAK-MAPK-dependent adhesion disassembly downstream of L1 contributes to semaphorin3A-induced collapse
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http://dx.doi.org/10.1038/emboj.2008.86
https://onlinelibrary.wiley.com/doi/abs/10.1038%2Femboj.2008.86
https://www.ncbi.nlm.nih.gov/pubmed/18464795
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https://pubmed.ncbi.nlm.nih.gov/PMC2426724
Volume 27
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