AUTHOR=Sabo Shasta L. , Lahr Jessica M. , Offer Madelyn , Weekes Anika LA , Sceniak Michael P. 

TITLE=GRIN2B-related neurodevelopmental disorder: current understanding of pathophysiological mechanisms

JOURNAL=Frontiers in Synaptic Neuroscience

VOLUME=Volume 14 - 2022

YEAR=2023

URL=https://www.frontiersin.org/journals/synaptic-neuroscience/articles/10.3389/fnsyn.2022.1090865

DOI=10.3389/fnsyn.2022.1090865

ISSN=1663-3563

ABSTRACT=GRIN2B-related neurodevelopmental disorder is a rare disease caused by mutations in the GRIN2B gene, which encodes the GluN2B subunit of NMDA receptors. Most individuals with GRIN2B-related neurodevelopmental disorder present with intellectual disability and developmental delay. Motor impairments, autism spectrum disorder, and epilepsy are also common. A large number of pathogenic de novo mutations have been identified in GRIN2B. However, it is not yet known how these mutations lead to the clinical symptoms of the disease. Recent research has begun to address this issue. Here, we describe key experimental approaches that have been used to better understand the pathophysiology of this disease. We discuss the impact of several distinct pathogenic GRIN2B mutations on NMDA receptor properties. We then critically review pivotal studies examining the synaptic and neurodevelopmental phenotypes observed when disease-associated GluN2B variants are expressed in neurons. These data provide compelling evidence that various GluN2B mutants interfere with neuronal differentiation, dendrite morphogenesis, synaptogenesis, and synaptic plasticity. Finally, we identify important open questions and considerations for future studies aimed at understanding this complex disease. Together, the existing data provide insight into the pathophysiological mechanisms that underlie GRIN2B-related neurodevelopmental disorder and emphasize the importance of comparing the effects of individual, disease associated mutations. Understanding the molecular, cellular and circuit phenotypes produced by a wide range of GRIN2B mutations should lead to identification core neurodevelopmental phenotypes that characterize the disease and lead to its symptoms. This information could help guide development and application of effective therapeutic strategies for treating individuals with GRIN2B-related neurodevelopmental disorder.