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Gene expression of neureguHn-1 isoforms in different brain regions of elderly schizophrenia patients

机译:老年精神分裂症患者不同区域神经元neureguHn-1亚型的基因表达

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摘要

One important risk gene in schizophrenia is neuregulin-1 (NRG1), which is expressed in different isoforms in the brain. To determine if alterations of NRG 1 are present in schizophrenia, we measured gene expression of NRG 1 and its main isoforms as well as the impact of genetic variation of NRG 1 in an exploratory study examining three brain regions instead of only one as published so far. In all, we examined post-mortem samples from 11 schizophrenia patients and eight normal subjects. We investigated gene expression of total NRG1 and isoforms I, II and III by real-time PCR in the prefrontal cortex (Brodmann areas 9 and 10) and right hippocampal tissue. For the genetic study, we genotyped the NRG1 polymorphism SNP8NRG221533, which is within the core haplotype of the original publication. Compared to controls, gene expression of the NRG1 isoform I was decreased and isoform II increased in the prefrontal cortex (BA10) of schizophrenia patients. There were no statistically significant differences between individuals carrying at least one C allele of SNP8NRG221533 compared to individuals homozygous for the T allele. The decreased expression of NRG1 isoform I and overexpression of isoform II may be related to deficits in receptor function as well as abnormal migration and myelination. However, our study sample was small and results of this exploratory study should be verified in a larger sample.
机译:精神分裂症的一个重要风险基因是神经调节蛋白1(NRG1),它在大脑中以不同的亚型表达。为了确定精神分裂症中是否存在NRG 1的改变,我们在一项探索性研究中测量了NRG 1及其主要同工型的基因表达以及NRG 1遗传变异的影响,该研究研究了三个大脑区域,而不是迄今仅公布的一个区域。总之,我们检查了11名精神分裂症患者和8名正常受试者的验尸样本。我们通过实时PCR在前额叶皮层(Brodmann区域9和10)和右海马组织中研究了总NRG1和同工型I,II和III的基因表达。对于遗传研究,我们对NRG1多态性SNP8NRG221533进行了基因分型,这是原始出版物的核心单倍型。与对照组相比,精神分裂症患者的前额叶皮层(BA10)中NRG1亚型I的基因表达降低,而亚型II的基因表达升高。与纯合T等位基因的个体相比,携带至少一个SNP8NRG221533 C等位基因的个体之间没有统计学上的显着差异。 NRG1亚型I的表达减少和亚型II的过表达可能与受体功能的缺失以及异常的迁移和髓鞘形成有关。但是,我们的研究样本很小,因此该探索性研究的结果应在更大的样本中进行验证。

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