Le trafic membranaire, un nouvel acteur du guidage axonal

Kathleen Zylbersztejn; Thierry Galli

doi:10.1051/medsci/2012283013

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Volume 28 / Numéro 3 (Mars 2012)

Med Sci (Paris), 28 3 (2012) 267-269

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Numéro		Med Sci (Paris) Volume 28, Numéro 3, Mars 2012


Page(s)		267 - 269
Section		Nouvelles
DOI		https://doi.org/10.1051/medsci/2012283013
Publié en ligne		6 avril 2012

Huber AB, Kolodkin AL, Ginty DD, Cloutier JF. Signaling at the growth cone: ligand-receptor complexes and the control of axon growth and guidance. Annu Rev Neurosci 2003 ; 26 : 509–563. [CrossRef] [PubMed] [Google Scholar]
Zylbersztejn K, Galli T. Vesicular traffic in cell navigation. FEBS J 2011 ; 278 : 4497–4505. [CrossRef] [PubMed] [Google Scholar]
Alberts P, Rudge R, Hinners I, et al. Cross talk between tetanus neurotoxin-insensitive vesicle-associated membrane protein-mediated transport and L1-mediated adhesion. Mol Biol Cell 2003 ; 14 : 4207–4220. [CrossRef] [PubMed] [Google Scholar]
Castellani V, Chedotal A, Schachner M, et al. Analysis of the L1-deficient mouse phenotype reveals cross-talk between Sema3A and L1 signaling pathways in axonal guidance. Neuron 2000 ; 27 : 237–249. [CrossRef] [PubMed] [Google Scholar]
Matsumoto H, Nagashima M. Netrin-1 elevates the level and induces cluster formation of its receptor DCC at the surface of cortical axon shafts in an exocytosis-dependent manner. Neurosci Res 2010 ; 67 : 99–107. [CrossRef] [PubMed] [Google Scholar]
Bouchard JF, Moore SW, Tritsch NX, et al. Protein kinase A activation promotes plasma membrane insertion of DCC from an intracellular pool: A novel mechanism regulating commissural axon extension. J Neurosci 2004 ; 24 : 3040–3050. [CrossRef] [PubMed] [Google Scholar]
Cotrufo T, Perez-Branguli F, Muhaisen A, et al. A signaling mechanism coupling netrin-1/deleted in colorectal cancer chemoattraction to SNARE-mediated exocytosis in axonal growth cones. J Neurosci 2011 ; 31 : 14463–14480. [CrossRef] [PubMed] [Google Scholar]
Zylbersztejn K, Petkovic M, Burgo A, et al. A vesicular SNARE required for Semaphorin 3A axonal repulsion. J Cell Biol 2012 ; 196 : 37–46. [CrossRef] [PubMed] [Google Scholar]
Pasterkamp RJ, Giger RJ. Semaphorin function in neural plasticity and disease. Curr Opin Neurobiol 2009 ; 19 : 263–274. [CrossRef] [PubMed] [Google Scholar]
Rizzolio S, Tamagnone L. Multifaceted role of neuropilins in cancer. Curr Med Chem 2011 ; 18 : 3563–3575. [CrossRef] [PubMed] [Google Scholar]
Proux-Gillardeaux V, Galli T. Rôle du trafic membranaire dans la migration cellulaire : Une nouvelle application pour les neurotoxines clostridiales ? Med Sci (Paris) 2005 ; 21 : 789. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
Tareste D. Énergie libérée par la machinerie de fusion SNAREpin. Med Sci (Paris) 2008 ; 24 : 142–143. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

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[1] Huber AB, Kolodkin AL, Ginty DD, Cloutier JF. Signaling at the growth cone: ligand-receptor complexes and the control of axon growth and guidance. Annu Rev Neurosci 2003 ; 26 : 509–563. [CrossRef] [PubMed] [Google Scholar]

[2] Zylbersztejn K, Galli T. Vesicular traffic in cell navigation. FEBS J 2011 ; 278 : 4497–4505. [CrossRef] [PubMed] [Google Scholar]

[3] Alberts P, Rudge R, Hinners I, et al. Cross talk between tetanus neurotoxin-insensitive vesicle-associated membrane protein-mediated transport and L1-mediated adhesion. Mol Biol Cell 2003 ; 14 : 4207–4220. [CrossRef] [PubMed] [Google Scholar]

[4] Castellani V, Chedotal A, Schachner M, et al. Analysis of the L1-deficient mouse phenotype reveals cross-talk between Sema3A and L1 signaling pathways in axonal guidance. Neuron 2000 ; 27 : 237–249. [CrossRef] [PubMed] [Google Scholar]

[5] Matsumoto H, Nagashima M. Netrin-1 elevates the level and induces cluster formation of its receptor DCC at the surface of cortical axon shafts in an exocytosis-dependent manner. Neurosci Res 2010 ; 67 : 99–107. [CrossRef] [PubMed] [Google Scholar]

[6] Bouchard JF, Moore SW, Tritsch NX, et al. Protein kinase A activation promotes plasma membrane insertion of DCC from an intracellular pool: A novel mechanism regulating commissural axon extension. J Neurosci 2004 ; 24 : 3040–3050. [CrossRef] [PubMed] [Google Scholar]

[7] Cotrufo T, Perez-Branguli F, Muhaisen A, et al. A signaling mechanism coupling netrin-1/deleted in colorectal cancer chemoattraction to SNARE-mediated exocytosis in axonal growth cones. J Neurosci 2011 ; 31 : 14463–14480. [CrossRef] [PubMed] [Google Scholar]

[8] Zylbersztejn K, Petkovic M, Burgo A, et al. A vesicular SNARE required for Semaphorin 3A axonal repulsion. J Cell Biol 2012 ; 196 : 37–46. [CrossRef] [PubMed] [Google Scholar]

[9] Pasterkamp RJ, Giger RJ. Semaphorin function in neural plasticity and disease. Curr Opin Neurobiol 2009 ; 19 : 263–274. [CrossRef] [PubMed] [Google Scholar]

[10] Rizzolio S, Tamagnone L. Multifaceted role of neuropilins in cancer. Curr Med Chem 2011 ; 18 : 3563–3575. [CrossRef] [PubMed] [Google Scholar]

[11] Proux-Gillardeaux V, Galli T. Rôle du trafic membranaire dans la migration cellulaire : Une nouvelle application pour les neurotoxines clostridiales ? Med Sci (Paris) 2005 ; 21 : 789. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

[12] Tareste D. Énergie libérée par la machinerie de fusion SNAREpin. Med Sci (Paris) 2008 ; 24 : 142–143. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]