| Literature DB >> 25374361 |
Katharine R Smith1, Katherine J Kopeikina1, Jessica M Fawcett-Patel1, Katherine Leaderbrand2, Ruoqi Gao1, Britta Schürmann1, Kristoffer Myczek1, Jelena Radulovic3, Geoffrey T Swanson4, Peter Penzes5.
Abstract
Recent evidence implicates glutamatergic synapses as key pathogenic sites in psychiatric disorders. Common and rare variants in the ANK3 gene, encoding ankyrin-G, have been associated with bipolar disorder, schizophrenia, and autism. Here we demonstrate that ankyrin-G is integral to AMPAR-mediated synaptic transmission and maintenance of spine morphology. Using superresolution microscopy we find that ankyrin-G forms distinct nanodomain structures within the spine head and neck. At these sites, it modulates mushroom spine structure and function, probably as a perisynaptic scaffold and barrier within the spine neck. Neuronal activity promotes ankyrin-G accumulation in distinct spine subdomains, where it differentially regulates NMDA receptor-dependent plasticity. These data implicate subsynaptic nanodomains containing a major psychiatric risk molecule, ankyrin-G, as having location-specific functions and open directions for basic and translational investigation of psychiatric risk molecules.Entities:
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Year: 2014 PMID: 25374361 PMCID: PMC4223651 DOI: 10.1016/j.neuron.2014.10.010
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173