Regulation of acetylcholine receptor clustering by the tumor suppressor APC

Nat Neurosci. 2003 Oct;6(10):1017-8. doi: 10.1038/nn1128. Epub 2003 Sep 21.

Abstract

At the developing neuromuscular junction, motor neuron-derived agrin triggers the differentiation of postsynaptic membrane into a highly specialized structure, where the nicotinic acetylcholine receptors (AChRs) are aggregated into high-density clusters. Agrin acts by activating the muscle-specific kinase MuSK and inducing coaggregation of the 43-kDa protein rapsyn with AChRs on muscle cell membrane. The signaling mechanism downstream of MuSK is poorly defined. We report here that the mouse tumor suppressor protein adenomatous polyposis coli (APC) has a role in AChR clustering and that the Wnt/beta-catenin pathway may crosstalk with agrin signaling cascade during synapse formation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenomatous Polyposis Coli Protein / metabolism*
  • Agrin / metabolism*
  • Agrin / pharmacology
  • Animals
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Cytoskeletal Proteins / metabolism
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / genetics
  • Mice
  • Muscle Denervation
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / metabolism
  • Muscle, Skeletal / embryology
  • Muscle, Skeletal / innervation*
  • Muscle, Skeletal / metabolism
  • Neuromuscular Junction / cytology
  • Neuromuscular Junction / embryology*
  • Neuromuscular Junction / metabolism
  • Protein Structure, Tertiary / drug effects
  • Protein Structure, Tertiary / physiology
  • Proto-Oncogene Proteins / metabolism
  • Receptor Aggregation / drug effects
  • Receptor Aggregation / physiology*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptors, Cholinergic / metabolism
  • Receptors, Nicotinic / drug effects
  • Receptors, Nicotinic / genetics
  • Receptors, Nicotinic / metabolism*
  • Recombinant Fusion Proteins / pharmacology
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Trans-Activators / metabolism
  • Wnt Proteins
  • Zebrafish Proteins*
  • beta Catenin

Substances

  • Adenomatous Polyposis Coli Protein
  • Agrin
  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • Proto-Oncogene Proteins
  • Receptors, Cholinergic
  • Receptors, Nicotinic
  • Recombinant Fusion Proteins
  • Trans-Activators
  • Wnt Proteins
  • Zebrafish Proteins
  • beta Catenin
  • MuSK protein, rat
  • Receptor Protein-Tyrosine Kinases