The formation of functional synapses requires a proper dialogue between incoming axons and their future synaptic targets. As axons approach their target, they are instructed to slow down and remodel to form proper presynaptic terminals. Although significant progress has been made in the identification of the mechanisms that control axon guidance, little is known about the mechanisms that regulate the conversion of actively growing axon into a presynaptic terminal. We found that Wnt secreted proteins are retrograde signals that regulate the terminal arborization of axons and synaptic differentiation. Wnts released from postsynaptic neurons induce extensive remodelling on incoming axons. This remodelling is manifested by a decrease in axon extension with a concomitant increase in growth-cone size. This morphological change is correlated with changes in the dynamics and organization of microtubules. Studies of a vertebrate synapse and the Drosophila neuromuscular junction suggest that a conserved Wnt signalling pathway modulates presynaptic microtubules as axons remodel during synapse formation. In this paper I discuss the role of the Wnt–Dvl (Dishevelled protein)–GSK-3β (glycogen synthase kinase-3β) signalling pathway in axon remodelling during synapse formation in the central nervous system.
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Conference Article|
October 26 2005
Retrograde signalling at the synapse: a role for Wnt proteins
P.C. Salinas
P.C. Salinas
1
1Department of Anatomy and Developmental Biology, University College London, University Street, London WC1E 6BT, U.K.
1email p.salinas@ucl.ac.uk
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Publisher: Portland Press Ltd
Received:
June 22 2005
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© 2005 The Biochemical Society
2005
Biochem Soc Trans (2005) 33 (6): 1295–1298.
Article history
Received:
June 22 2005
Citation
P.C. Salinas; Retrograde signalling at the synapse: a role for Wnt proteins. Biochem Soc Trans 26 October 2005; 33 (6): 1295–1298. doi: https://doi.org/10.1042/BST0331295
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