SHANKAstro

Overview

Project Summary

The lack of one copy of the SHANK3 gene is the main cause of the neuropsychiatric symptoms of Phelan-McDermid syndrome (PMS), a neurodevelopmental disorder characterised by intellectual disability and autistic-like deficits. To date, SHANK3-related syndromes have only been investigated from a neuronal perspective, but recent data have highlighted a possible involvement of astrocytic SHANK3 in the pathophysiology of PMS. Astrocyte-specific deletion of SHANK3 early in postnatal development is associated with impaired astrocyte maturation and recapitulates many of the main phenotypes of PMS mouse models, such as impaired synaptogenesis, repetitive behaviours and cognitive dysfunction. These findings suggest that defects in the postnatal maturation of SHANK3 deficient astrocytes may (at least partially) account for the neuronal dysmorphogenesis, synaptopathies, and behavioural impairments associated with SHANK3-related syndromes. By deleting and re-expressing astrocyte-specific SHANK3 in systems ranging from in vitro cultures to state-of-the-art animal models and next-generation brain organoids, we will be able to provide important new insights into the pathological mechanisms of neurodevelopment in PMS. These could guide development of therapies for PMS, and possibly other autism-spectrum disorders characterised by mGluR5 signalling dysfunction.

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