Upper cortical layer–driven network impairment in schizophrenia

Author:

Batiuk Mykhailo Y.1ORCID,Tyler Teadora2ORCID,Dragicevic Katarina1ORCID,Mei Shenglin3ORCID,Rydbirk Rasmus1ORCID,Petukhov Viktor1ORCID,Deviatiiarov Ruslan45ORCID,Sedmak Dora6ORCID,Frank Erzsebet2,Feher Virginia2,Habek Nikola6ORCID,Hu Qiwen3,Igolkina Anna37,Roszik Lilla2,Pfisterer Ulrich1,Garcia-Gonzalez Diego1ORCID,Petanjek Zdravko6ORCID,Adorjan Istvan2,Kharchenko Peter V.3ORCID,Khodosevich Konstantin1ORCID

Affiliation:

1. Biotech Research and Innovation Centre (BRIC), Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

2. Department of Anatomy, Histology and Embryology, Semmelweis University, Budapest H-1085, Hungary.

3. Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.

4. The National Center for Personalized Medicine of Endocrine Diseases, Moscow 115478, Russia.

5. Kazan Federal University, Kazan 420043, Russia.

6. Croatian Institute for Brain Research and Center of Excellence for Basic, Clinical and Translational Neuroscience, School of Medicine, University of Zagreb, Zagreb 10000, Croatia.

7. St. Petersburg Polytechnical University, St. Petersburg 195251, Russia.

Abstract

Schizophrenia is one of the most widespread and complex mental disorders. To characterize the impact of schizophrenia, we performed single-nucleus RNA sequencing (snRNA-seq) of >220,000 neurons from the dorsolateral prefrontal cortex of patients with schizophrenia and matched controls. In addition, >115,000 neurons were analyzed topographically by immunohistochemistry. Compositional analysis of snRNA-seq data revealed a reduction in abundance of GABAergic neurons and a concomitant increase in principal neurons, most pronounced for upper cortical layer subtypes, which was substantiated by histological analysis. Many neuronal subtypes showed extensive transcriptomic changes, the most marked in upper-layer GABAergic neurons, including down-regulation in energy metabolism and up-regulation in neurotransmission. Transcription factor network analysis demonstrated a developmental origin of transcriptomic changes. Last, Visium spatial transcriptomics further corroborated upper-layer neuron vulnerability in schizophrenia. Overall, our results point toward general network impairment within upper cortical layers as a core substrate associated with schizophrenia symptomatology.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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