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IRSp53 (also known as BAIAP2) is a multi-domain scaffolding and adaptor protein that has been implicated in the regulation of membrane and actin dynamics at subcellular structures, including filopodia and lamellipodia. Accumulating evidence indicates that IRSp53 is an abundant component of the postsynaptic density at excitatory synapses and an important regulator of actin-rich dendritic spines. In addition, IRSp53 has been implicated in diverse psychiatric disorders, including autism spectrum disorders, schizophrenia, and attention deficit/hyperactivity disorder. Mice lacking IRSp53 display enhanced NMDA (N-methyl-d-aspartate) receptor function accompanied by social and cognitive deficits, which are reversed by pharmacological suppression of NMDA receptor function. These results suggest the hypothesis that defective actin/membrane modulation in IRSp53-deficient dendritic spines may lead to social and cognitive deficits through NMDA receptor dysfunction. This article is part of the Special Issue entitled 'Synaptopathy--from Biology to Therapy'.

More information Original publication

DOI

10.1016/j.neuropharm.2015.06.019

Type

Journal article

Publication Date

2016-01-01T00:00:00+00:00

Volume

100

Pages

27 - 39

Total pages

12

Keywords

Actin, Dendritic spine, IRSp53, Membrane, NMDA receptor, Psychiatric disorders, Actin Cytoskeleton, Animals, Brain, Cell Membrane, Dendritic Spines, Humans, Mental Disorders, Mice, Nerve Tissue Proteins, Phenotype, Post-Synaptic Density, Protein Interaction Domains and Motifs, RNA, Messenger, Receptors, N-Methyl-D-Aspartate