Increased number of excitatory synapsis and decreased number of inhibitory synapsis in the prefrontal cortex in autism

Author:

Vakilzadeh Gelareh12,Maseko Busisiwe C3,Bartely Trevor D12,McLennan Yingratana A12,Martínez-Cerdeño Verónica124

Affiliation:

1. , University of California, Davis School of Medicine Department of Pathology and Laboratory Medicine , Sacramento, CA, United States

2. Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children , Sacramento, CA, United States

3. University of the Witwatersrand Faculty of health Sciences, School of Anatomical Sciences, , Johannesburg, The Republic of South Africa

4. MIND Institute, UC Davis School of Medicine , Sacramento, CA, United States

Abstract

Abstract Previous studies in autism spectrum disorder demonstrated an increased number of excitatory pyramidal cells and a decreased number of inhibitory parvalbumin+ chandelier interneurons in the prefrontal cortex of postmortem brains. How these changes in cellular composition affect the overall abundance of excitatory and inhibitory synapses in the cortex is not known. Herein, we quantified the number of excitatory and inhibitory synapses in the prefrontal cortex of 10 postmortem autism spectrum disorder brains and 10 control cases. To identify excitatory synapses, we used VGlut1 as a marker of the presynaptic component and postsynaptic density protein-95 as marker of the postsynaptic component. To identify inhibitory synapses, we used the vesicular gamma-aminobutyric acid transporter as a marker of the presynaptic component and gephyrin as a marker of the postsynaptic component. We used Puncta Analyzer to quantify the number of co-localized pre- and postsynaptic synaptic components in each area of interest. We found an increase in the number of excitatory synapses in upper cortical layers and a decrease in inhibitory synapses in all cortical layers in autism spectrum disorder brains compared with control cases. The alteration in the number of excitatory and inhibitory synapses could lead to neuronal dysfunction and disturbed network connectivity in the prefrontal cortex in autism spectrum disorder.

Funder

NIMH

Shriners Hospitals

Publisher

Oxford University Press (OUP)

Reference68 articles.

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