| Literature DB >> 24336150 |
Michael A Bemben1, Seth L Shipman2, Takaaki Hirai3, Bruce E Herring2, Yan Li4, John D Badger3, Roger A Nicoll5, Jeffrey S Diamond6, Katherine W Roche3.
Abstract
Neuroligins are postsynaptic cell adhesion molecules that are important for synaptic function through their trans-synaptic interaction with neurexins (NRXNs). The localization and synaptic effects of neuroligin-1 (NL-1, also called NLGN1) are specific to excitatory synapses with the capacity to enhance excitatory synapses dependent on synaptic activity or Ca(2+)/calmodulin kinase II (CaMKII). Here we report that CaMKII robustly phosphorylates the intracellular domain of NL-1. We show that T739 is the dominant CaMKII site on NL-1 and is phosphorylated in response to synaptic activity in cultured rodent neurons and sensory experience in vivo. Furthermore, a phosphodeficient mutant (NL-1 T739A) reduces the basal and activity-driven surface expression of NL-1, leading to a reduction in neuroligin-mediated excitatory synaptic potentiation. To the best of our knowledge, our results are the first to demonstrate a direct functional interaction between CaMKII and NL-1, two primary components of excitatory synapses.Entities:
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Year: 2013 PMID: 24336150 PMCID: PMC3943352 DOI: 10.1038/nn.3601
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884