PUBLICATION

Initiation of synapse formation by Wnt-induced MuSK endocytosis

Authors
Gordon, L.R., Gribble, K.D., Syrett, C.M., and Granato, M.
ID
ZDB-PUB-120215-7
Date
2012
Source
Development (Cambridge, England)   139(5): 1023-1033 (Journal)
Registered Authors
Granato, Michael
Keywords
zebrafish, muscle specific kinase, MuSK, unplugged, wnt11, dishevelled, rab11, recycling endosome, neuromuscular junction, planar cell polarity, AChR pre-pattern, motor axons
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Cell Membrane/metabolism
  • Cell Polarity
  • Endocytosis/physiology*
  • Endosomes/metabolism
  • Muscle, Skeletal/cytology
  • Muscle, Skeletal/physiology
  • Receptor Protein-Tyrosine Kinases/genetics
  • Receptor Protein-Tyrosine Kinases/metabolism*
  • Receptors, Cholinergic/metabolism
  • Recombinant Fusion Proteins/genetics
  • Recombinant Fusion Proteins/metabolism
  • Synapses/physiology*
  • Synapses/ultrastructure
  • Wnt Proteins/genetics
  • Wnt Proteins/metabolism*
  • Wnt Signaling Pathway/physiology*
  • Wnt4 Protein/genetics
  • Wnt4 Protein/metabolism*
  • Zebrafish
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
  • rab GTP-Binding Proteins/genetics
  • rab GTP-Binding Proteins/metabolism
PubMed
22318632 Full text @ Development
Abstract

In zebrafish, the MuSK receptor initiates neuromuscular synapse formation by restricting presynaptic growth cones and postsynaptic acetylcholine receptors (AChRs) to the center of skeletal muscle cells. Increasing evidence suggests a role for Wnts in this process, yet how muscle cells respond to Wnt signals is unclear. Here, we show that in vivo, wnt11r and wnt4a initiate MuSK translocation from muscle membranes to recycling endosomes and that this transition is crucial for AChR accumulation at future synaptic sites. Moreover, we demonstrate that components of the planar cell polarity pathway colocalize to recycling endosomes and that this localization is MuSK dependent. Knockdown of several core components disrupts MuSK translocation to endosomes, AChR localization and axonal guidance. We propose that Wnt-induced trafficking of the MuSK receptor to endosomes initiates a signaling cascade to align pre- with postsynaptic elements. Collectively, these findings suggest a general mechanism by which Wnt signals shape synaptic connectivity through localized receptor endocytosis.

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