Pharmacological modulation of developmental and synaptic phenotypes in human SHANK3 deficient stem cell-derived neuronal models

Author:

Thibaudeau Amandine,Schmitt Karen,François Louise,Chatrousse Laure,Hoffmann David,Cousin Loic,Weiss Amélie,Vuidel Aurore,Jacob Christina B.,Sommer PeterORCID,Benchoua Alexandra,Wilbertz Johannes H.ORCID

Abstract

AbstractPhelan-McDermid syndrome (PMDS) arises from mutations in the terminal region of chromosome 22q13, impacting the SHANK3 gene. The resulting deficiency of the postsynaptic density scaffolding protein SHANK3 is associated with autism spectrum disorder (ASD). We examined 12 different PMDS patient and CRISPR-engineered stem cell-derived neuronal models and controls and found that reduced expression of SHANK3 leads to neuronal hyperdifferentiation, increased synapse formation, and decreased neuronal activity. We performed automated imaging-based screening of 7,120 target-annotated small molecules and identified three compounds that rescued SHANK3-dependent neuronal hyperdifferentiation. One compound, Benproperine, rescued the decreased colocalization of Actin Related Protein 2/3 Complex Subunit 2 (ARPC2) with ß-actin and rescued increased synapse formation in SHANK3 deficient neurons when administered early during differentiation. Neuronal activity was only mildly affected, highlighting Benproperine’s effects as a neurodevelopmental modulator. This study demonstrates that small molecular compounds that reverse developmental phenotypes can be identified in human neuronal PMDS models.

Funder

Programme d'investissements d'avenir (PIA) by the Secrétariat général pour l'investissement (SGPI) of the French government

I-STEM is supported by a recurrent annual grant of the Association Française contre les Myopathies (AFM-Téléthon).

Publisher

Springer Science and Business Media LLC

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