Abstract
The maintenance of spine and synapse number during development is critical for neuronal circuit formation and function. Here we show that δ-catenin, a component of the cadherin-catenin cell adhesion complex, regulates spine and synapse morphogenesis during development. Genetic ablation or acute knockdown of δ-catenin leads to increases in spine and synapse density, accompanied by a decrease in tetrodotoxin induced spine plasticity. Our results indicate that δ-catenin may mediate conversion of activity-dependent signals to morphological spine plasticity. The functional role of δ-catenin in regulating spine density does not require binding to cadherins, but does require interactions with PDZ domain-containing proteins. We propose that the perturbations in spine and synaptic structure and function observed after depletion of δ-catenin during development may contribute to functional alterations in neural circuitry, the cognitive deficits observed in mutant mice, and the mental retardation pathology of Cri-du-chat syndrome. Copyright © 2009 Society for Neuroscience.
Cite
CITATION STYLE
Arikkath, J., Peng, I. F., Yu, G. N., Israely, I., Liu, X., Ullian, E. M., & Reichardt, L. F. (2009). δ-catenin regulates spine and synapse morphogenesis and function in hippocampal neurons during development. Journal of Neuroscience, 29(17), 5435–5442. https://doi.org/10.1523/JNEUROSCI.0835-09.2009
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.