Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/38401

Emergent Growth Cone Responses to Combinations of Slit1 and Netrin 1 in Thalamocortical Axon Topography


thumbnail_pdf
View/Open:
 Emergent Growth Cone Responses.pdf

1,89 MB
Adobe PDF
Share:
Title:
Emergent Growth Cone Responses to Combinations of Slit1 and Netrin 1 in Thalamocortical Axon Topography
Authors:
Bielle, Franck
Marcos-Mondéjar, Paula
Leyva-Díaz, Eduardo  
Lokmane, Ludmilla  
Mire, Erik  
Mailhes, Caroline
Keita, Maryama
García, Noelia
Tessier-Lavigne, Marc  
GAREL, Sonia  
López-Bendito, Guillermina  
Editor:
Elsevier
Issue Date:
2011-10
URI:
https://hdl.handle.net/11000/38401
Abstract:
How guidance cues are integrated during the formation of complex axonal tracts remains largely unknown. Thalamocortical axons (TCAs), which convey sensory and motor information to the neocortex, have a rostrocaudal topographic organization initially established within the ventral telencephalon [1-3]. Here, we show that this topography is set in a small hub, the corridor, which contains matching rostrocaudal gradients of Slit1 and Netrin 1. Using in vitro and in vivo experiments, we show that Slit1 is a rostral repellent that positions intermediate axons. For rostral axons, although Slit1 is also repulsive and Netrin 1 has no chemotactic activity, the two factors combined generate attraction. These results show that Slit1 has a dual context-dependent role in TCA pathfinding and furthermore reveal that a combination of cues produces an emergent activity that neither of them has alone. Our study thus provides a novel framework to explain how a limited set of guidance cues can generate a vast diversity of axonal responses necessary for proper wiring of the nervous system.
Keywords/Subjects:
thalamocortical axons
guidance cues
nervous system
Type of document:
info:eu-repo/semantics/article
Access rights:
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
DOI:
10.1016/j.cub.2011.09.008
Published in:
Curr Biol . 2011 Oct 25;21(20):1748-55
Appears in Collections:
Instituto de Neurociencias



Creative Commons ???jsp.display-item.text9???