Concordance of Immune-Related Markers in Lymphocytes and Prefrontal Cortex in Schizophrenia

Author:

Gatta Eleonora1,Saudagar Vikram1,Drnevich Jenny2,Forrest Marc P3,Auta James1,Clark Lindsay V2,Sershen Henry45,Smith Robert C45,Grayson Dennis R1,Davis John M6,Guidotti Alessandro1

Affiliation:

1. Center for Alcohol Research in Epigenetics, Psychiatric Institute, Department of Psychiatry, College of Medicine, University of Illinois at Chicago, Chicago, IL

2. High-Performance Biological Computing, Roy J. Carver Biotechnology Center, University of Illinois-Urbana Champaign, Urbana, IL

3. Department of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL

4. Nathan Kline Institute for Psychiatric Research, Orangeburg, NY

5. Department of Psychiatry, NYU Langone Medical Center, New York, NY

6. Psychiatric Institute, Department of Psychiatry, College of Medicine, University of Illinois at Chicago, Chicago, IL

Abstract

Abstract Schizophrenia is a severe neuropsychiatric disorder associated with a wide array of transcriptomic and neurobiochemical changes. Genome-wide transcriptomic profiling conducted in postmortem brain have provided novel insights into the pathophysiology of this disorder, and identified biological processes including immune/inflammatory-related responses, metabolic, endocrine, and synaptic function. However, few studies have investigated whether similar changes are present in peripheral tissue. Here, we used RNA-sequencing to characterize transcriptomic profiles of lymphocytes in 18 nonpsychotic controls and 19 individuals with schizophrenia. We identified 2819 differentially expressed transcripts (Pnominal < .05) in the schizophrenia group when compared to controls. Bioinformatic analyses conducted on a subset of 293 genes (Pnominal < .01 and |log2 FC| > 0.5) highlighted immune/inflammatory responses as key biological processes in our dataset. Differentially expressed genes in lymphocytes were highly enriched in gene expression profiles associated with cortex layer 5a and immune cells. Thus, we investigated whether the changes in transcripts levels observed in lymphocytes could also be detected in the prefrontal cortex (PFC, BA10) in a second replication cohort of schizophrenia subjects. Remarkably, mRNA levels detected in the PFC and lymphocytes were in strong agreement, and measurements obtained using RNA-sequencing positively correlated with data obtained by reverse transcriptase-quantitative polymerase chain reaction analysis. Collectively, our work supports a role for immune dysfunction in the pathogenesis of schizophrenia and suggests that peripheral markers can be used as accessible surrogates to investigate putative central nervous system disruptions.

Funder

National Institute of Mental Health

National Institute on Alcohol Abuse and Alcoholism

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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