Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome
Filomena Grazia Alvino, Silvia Gini, Antea Minetti, Marco Pagani, David Sastre-Yagüe, Noemi Barsotti, A. Elizabeth de Guzman, Charles Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Wendy R. Kates, Declan Murphy, Michael Lombardo, Massimo Pasqualetti, Carrie E. Bearden, Alessandro Gozzi
Abstract
Chromosome 22q11.2 deletion increases the risk of neuropsychiatric disorders like autism and schizophrenia. Disruption of large-scale functional connectivity in 22q11 deletion syndrome (22q11DS) has been widely reported, but the biological factors driving these changes remain unclear. We used a cross-species design to uncover the developmental trajectory and neural underpinnings of brain dysconnectivity in 22q11DS. In LgDel mice, a model for 22q11DS, we found age-specific patterns of brain dysconnectivity, with widespread fMRI hyperconnectivity in juvenile mice reconfiguring to hippocampal hypoconnectivity over puberty. These changes correlated with developmental alterations in dendritic spine density, and both were transiently normalized by GSK3β inhibition, suggesting a synaptic origin for this phenomenon. Notably, analogous pubertal hyperconnectivity-to-hypoconnectivity reconfiguration occurs in human 22q11DS, affecting cortical regions enriched for GSK3β-associated synaptic genes and autism-relevant transcripts. This dysconnectivity also predicts age-dependent social alterations in 22q11DS individuals. These results suggest that synaptic mechanisms underlie developmental brain dysconnectivity in 22q11DS.