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Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium

机译:与精神分裂症认知缺陷相关的分子标记:活检嗅觉神经上皮细胞的研究

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Cognitive impairment is a key feature of schizophrenia (SZ) and determines functional outcome. Nonetheless, molecular signatures in neuronal tissues that associate with deficits are not well understood. We conducted nasal biopsy to obtain olfactory epithelium from patients with SZ and control subjects. The neural layers from the biopsied epithelium were enriched by laser-captured microdissection. We then performed an unbiased microarray expression study and implemented a systematic neuropsychological assessment on the same participants. The differentially regulated genes in SZ were further filtered based on correlation with neuropsychological traits. This strategy identified the SMAD 5 gene, and real-time quantitative PCR analysis also supports downregulation of the SMAD pathway in SZ. The SMAD pathway has been important in multiple tissues, including the role for neurodevelopment and bone formation. Here the involvement of the pathway in adult brain function is suggested. This exploratory study establishes a strategy to better identify neuronal molecular signatures that are potentially associated with mental illness and cognitive deficits. We propose that the SMAD pathway may be a novel target in addressing cognitive deficit of SZ in future studies.
机译:认知障碍是精神分裂症(SZ)的关键特征,并决定功能预后。然而,与缺陷相关的神经元组织中的分子标记尚未被很好地理解。我们进行了鼻腔活检,以从SZ患者和对照对象中获取嗅觉上皮。活检上皮的神经层通过激光捕获显微解剖得以富集。然后,我们进行了无偏差的微阵列表达研究,并对相同的参与者进行了系统的神经心理学评估。基于与神经心理学特征的相关性,进一步过滤了SZ中的差异调节基因。该策略确定了SMAD 5基因,实时定量PCR分析也支持SZ中SMAD途径的下调。 SMAD途径在多种组织中很重要,包括对神经发育和骨骼形成的作用。在此建议该途径参与成人脑功能。这项探索性研究建立了一种策略,可以更好地识别可能与精神疾病和认知缺陷有关的神经元分子信号。我们建议SMAD途径可能是在未来的研究中解决SZ认知缺陷的新目标。

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