Integrative Transcriptomics Reveals Layer 1 Astrocytes Altered in Schizophrenia
Julio LeoniD, Satoshi YoshinagaiD, Mizuki HinoiD, Atsuko NagaokaiD, Yoshinari AndoiD, Jonathan MoodyiD, Miki Kojima, Ayako Kitazawa, Kanehiro HayashiiD, Kazunori NakajimaiD, Carlo CondelloiD, Piero CarninciiD, Yasuto KuniiiD, Chung-Chau HoniD, Jay W. ShiniD, Ken‐ichiro KuboiD
Abstract
Schizophrenia is one of the most prevalent psychiatric disorders with unclear pathophysiology despite a century-long history of intense research. Schizophrenia affects multiple networks across different brain regions. The anterior cingulate cortex (ACC) is the region that connects the limbic system to cognitive areas such as the prefrontal cortex and represents a pivotal region for the etiology of schizophrenia; however, the molecular pathology, considering its cellular and anatomical complexity, is not well understood. Here, we performed an integrative analysis of spatial and single-nucleus transcriptomics of the postmortem ACC of people with schizophrenia, together with a thorough histological analysis. The data revealed major transcriptomics signatures altered in schizophrenia, pointing at the dysregulation of glial cells, primarily in astrocytes. We further discovered a decrease in the cellular density and abundance of processes of interlaminar astrocytes, a subpopulation of astrocytes specific to primates that localize in the layer 1 and influence the superficial cortical microenvironment across layer 1 and layers 2/3 of the cortex. Our study suggests that aberrant changes in interlaminar astrocytes could explain the cell-to-cell circuit alterations found in schizophrenia and represent novel therapeutic targets to ameliorate schizophrenia-associated dysfunction.
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