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

Schizophrenia Bulletin Open Pub Date : 2021-02-06 eCollection Date: 2021-01-01 DOI:10.1093/schizbullopen/sgab002
Eleonora Gatta, Vikram Saudagar, Jenny Drnevich, Marc P Forrest, James Auta, Lindsay V Clark, Henry Sershen, Robert C Smith, Dennis R Grayson, John M Davis, Alessandro Guidotti
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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 (P nominal < .05) in the schizophrenia group when compared to controls. Bioinformatic analyses conducted on a subset of 293 genes (P nominal < .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.

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精神分裂症患者淋巴细胞和前额叶皮层免疫相关标志物的一致性。
精神分裂症是一种严重的神经精神疾病,与广泛的转录组学和神经生化变化有关。在死后大脑中进行的全基因组转录组分析为这种疾病的病理生理学提供了新的见解,并确定了包括免疫/炎症相关反应、代谢、内分泌和突触功能在内的生物过程。然而,很少有研究调查外周组织是否存在类似的变化。在这里,我们使用rna测序来表征18名非精神病对照和19名精神分裂症患者的淋巴细胞转录组谱。与对照组相比,我们在精神分裂症组中发现了2819个差异表达转录本(P < 0.05)。对293个基因子集(P < 0.01和|log2 FC| > 0.5)进行的生物信息学分析强调了免疫/炎症反应是我们数据集中的关键生物过程。淋巴细胞中差异表达基因在皮层5a和免疫细胞相关基因表达谱中高度富集。因此,我们研究了在精神分裂症患者的第二个复制队列中,淋巴细胞中观察到的转录本水平的变化是否也可以在前额皮质(PFC, BA10)中检测到。值得注意的是,PFC和淋巴细胞中检测到的mRNA水平非常一致,使用rna测序获得的测量结果与逆转录-定量聚合酶链反应分析获得的数据呈正相关。总的来说,我们的工作支持了免疫功能障碍在精神分裂症发病机制中的作用,并表明外周标记物可以作为研究假定的中枢神经系统紊乱的可获得的替代物。
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