Neurexin-neuroligin cell adhesion complexes contribute to synaptotropic dendritogenesis via growth stabilization mechanisms in vivo.

TitleNeurexin-neuroligin cell adhesion complexes contribute to synaptotropic dendritogenesis via growth stabilization mechanisms in vivo.
Publication TypeJournal Article
Year of Publication2010
AuthorsChen SXuan, Tari PKarimi, She K, Haas K
Date Published2010 Sep 23
KeywordsAnimals, Animals, Genetically Modified, Cell Adhesion Molecules, Neuronal, Dendrites, Excitatory Postsynaptic Potentials, Gene Expression Regulation, Developmental, Imaging, Three-Dimensional, Immunoprecipitation, Larva, Luminescent Proteins, Membrane Potentials, Microscopy, Confocal, Mutation, Nerve Tissue Proteins, Neurotoxins, Pseudopodia, Receptors, AMPA, Superior Colliculi, Synapses, Synaptic Transmission, Synaptosomal-Associated Protein 25, Time Factors, Xenopus

Cell adhesion molecules are well characterized for mediating synapse initiation, specification, differentiation, and maturation, yet their contribution to directing dendritic arborization during early brain circuit formation remains unclear. Using two-photon time-lapse imaging of growing neurons within intact and awake embryonic Xenopus brain, we examine roles of β-neurexin (NRX) and neuroligin-1 (NLG1) in dendritic arbor development. Using methods of dynamic morphometrics for comprehensive 3D quantification of rapid dendritogenesis, we find initial trans-synaptic NRX-NLG1 adhesions confer transient morphologic stabilization independent of NMDA receptor activity, whereas persistent stabilization requires NMDA receptor-dependent synapse maturation. Disrupting NRX-NLG1 function destabilizes filopodia while reducing synaptic density and AMPA receptor mEPSC frequency. Altered dynamic growth culminates in reduced dendritic arbor complexity as neurons mature over days. These results expand the synaptotropic model of dendritogenesis to incorporate cell adhesion molecule-mediated morphological stabilization necessary for directing normal dendritic arborization, providing a potential morphological substrate for developmental cognitive impairment associated with cell adhesion molecule mutations.

Alternate JournalNeuron
PubMed ID20869594
Grant List / / Canadian Institutes of Health Research / Canada