Beta-catenin is critical for dendritic morphogenesis

Nat Neurosci. 2003 Nov;6(11):1169-77. doi: 10.1038/nn1132. Epub 2003 Oct 5.

Abstract

Regulated growth and arborization of dendritic processes are critical to the formation of functional neuronal networks. Here we identify beta-catenin as a critical mediator of dendritic morphogenesis. We found that increasing the intracellular levels of beta-catenin and other members of the cadherin/catenin complex, namely N-cadherin and alphaN-catenin, enhances dendritic arborization in rat hippocampal neurons, an effect that does not require Wnt/beta-catenin-dependent transcription. Conversely, proteins that sequester beta-catenin decreased dendritic branch tip number and total dendritic branch length. Enhancement of dendritic growth elicited by depolarization requires beta-catenin and increased Wnt release. These results identify Wnt/beta-catenin signaling as an important mediator of dendritic development and suggest that the intracellular level of the cadherin/catenin complex is a limiting factor during critical stages of dendritic morphogenesis.

Publication types

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

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology
  • Anesthetics, Local / pharmacology
  • Animals
  • Animals, Newborn
  • Cadherins / metabolism
  • Calcium Channel Blockers / pharmacology
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cells, Cultured
  • Culture Media, Conditioned / pharmacology
  • Cytoskeletal Proteins / physiology*
  • DNA-Binding Proteins / metabolism
  • Dendrites / drug effects
  • Dendrites / physiology*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Embryo, Mammalian
  • Epitopes / metabolism
  • Excitatory Amino Acid Antagonists / pharmacology
  • Gene Expression Regulation, Developmental
  • Green Fluorescent Proteins
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Humans
  • Kidney
  • Luminescent Proteins / metabolism
  • Lymphoid Enhancer-Binding Factor 1
  • Morphogenesis / drug effects
  • Morphogenesis / physiology*
  • Mutation
  • Neurons / cytology*
  • Neurons / drug effects
  • Nifedipine / pharmacology
  • Potassium Chloride / pharmacology
  • Probability
  • Proto-Oncogene Proteins / antagonists & inhibitors
  • Proto-Oncogene Proteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Sodium Chloride / pharmacology
  • Tetrodotoxin / pharmacology
  • Trans-Activators / physiology*
  • Transcription Factors / metabolism
  • Transfection
  • Wnt Proteins
  • Zebrafish Proteins*
  • beta Catenin
  • rho GTP-Binding Proteins / metabolism

Substances

  • Anesthetics, Local
  • CTNNB1 protein, human
  • Cadherins
  • Calcium Channel Blockers
  • Ctnnb1 protein, rat
  • Culture Media, Conditioned
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • Epitopes
  • Excitatory Amino Acid Antagonists
  • Luminescent Proteins
  • Lymphoid Enhancer-Binding Factor 1
  • Proto-Oncogene Proteins
  • Trans-Activators
  • Transcription Factors
  • Wnt Proteins
  • Zebrafish Proteins
  • beta Catenin
  • Green Fluorescent Proteins
  • Tetrodotoxin
  • Sodium Chloride
  • Potassium Chloride
  • 2-Amino-5-phosphonovalerate
  • Calcium-Calmodulin-Dependent Protein Kinases
  • rho GTP-Binding Proteins
  • Nifedipine