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Molecular evidence for increased expression of genes related to immune and chaperone function in the prefrontal cortex in schizophrenia.精神分裂症患者前额叶皮质中与免疫和伴侣功能相关基因表达增加的分子证据。
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精神分裂症患者前额叶皮层的亚颗粒基因表达紊乱:神经发育改变的特征?

Infragranular gene expression disturbances in the prefrontal cortex in schizophrenia: signature of altered neural development?

机构信息

Department of Psychiatry, U of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.

出版信息

Neurobiol Dis. 2010 Mar;37(3):738-46. doi: 10.1016/j.nbd.2009.12.013. Epub 2009 Dec 23.

DOI:10.1016/j.nbd.2009.12.013
PMID:20034564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2823856/
Abstract

The development of the human neocortex gives rise to a complex cytoarchitecture, grouping together cells with similar structure, connectivity and function. As a result, the six neocortical laminae show distinct molecular content. In schizophrenia, many anatomical and neurochemical changes appear to be restricted to a subset of lamina and/or cell types. In this study, we hypothesized that supragranular (SG; laminae II-III) and infragranular layers (IG; laminae V-VI) of area 46 in the human prefrontal cortex will show distinct and specific transcriptome alterations between subjects with schizophrenia and matched controls. To enhance sample homogeneity, we compared the gene expression patterns of the SG and IG layers of 8 matched middle-aged male subjects with schizophrenia to 8 pairwise matched controls using two replicate DNA microarrays for each sample. The study revealed strong disease-related laminar expression differences between the SG and IG layers. Expression changes were dominated by an overall underexpression of the IG-enriched genes in the schizophrenia subjects compared to normal control subjects. Furthermore, using a diagnosis-blind, unsupervised clustering of the control-derived SG or IG-enriched transcripts, the IG-enriched markers segregated the subjects with schizophrenia from the matched controls with a high degree of confidence. Importantly, multiple members of the semaphorin gene family reported altered gene expression, suggesting that the IG gene expression disturbances in subjects with schizophrenia may be a result of altered cortical development and disrupted brain connectivity.

摘要

人类新皮层的发育产生了复杂的细胞结构,将具有相似结构、连接和功能的细胞分组在一起。因此,六层新皮层显示出明显不同的分子含量。在精神分裂症中,许多解剖和神经化学变化似乎仅限于部分层和/或细胞类型。在这项研究中,我们假设在人类前额叶皮层的 46 区的颗粒上层(SG;层 II-III)和颗粒下层(IG;层 V-VI)之间,精神分裂症患者和匹配对照组之间会出现明显而特定的转录组改变。为了增强样本的同质性,我们使用两个重复的 DNA 微阵列对每个样本进行比较,将 8 名匹配的中年男性精神分裂症患者和 8 名配对的对照组的 SG 和 IG 层的基因表达模式进行了比较。研究结果显示,SG 和 IG 层之间存在强烈的疾病相关的分层表达差异。与正常对照组相比,精神分裂症患者的 IG 丰富基因总体表达不足,这是表达变化的主要原因。此外,使用无监督聚类对源自对照的 SG 或 IG 丰富的转录本进行聚类,IG 丰富的标记可以高度置信地将精神分裂症患者与匹配的对照组区分开来。重要的是,多种神经丝蛋白基因家族的成员报告了改变的基因表达,这表明精神分裂症患者的 IG 基因表达紊乱可能是皮质发育改变和脑连接中断的结果。