首页> 外文期刊>Journal of psychiatry & neuroscience: JPN >MicroRNA-137 regulates a glucocorticoid receptor-dependent signalling network: Implications for the etiology of schizophrenia
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MicroRNA-137 regulates a glucocorticoid receptor-dependent signalling network: Implications for the etiology of schizophrenia

机译:MicroRNA-137调节糖皮质激素受体依赖性信号传导网络:对精神分裂症的病因学意义

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Background: Schizophrenia is a highly heritable neurodevelopmental disorder. A genetic variant of microRNA-137 (miR-137) has yielded significant genome-wide association with schizophrenia, suggesting that this miRNA plays a key role in its etiology. Therefore, a molecular network of interacting miR-137 targets may provide insights into the biological processes underlying schizophrenia. Methods:We first used bioinformatics tools to obtain and analyze predicted human and mouse miR-137 targets. We then determined miR-137 levels in rat barrel cortex after environmental enrichment (EE), a neuronal plasticity model that induces upregulation of several predicted miR-137 targets. Subsequently, expression changes of these predicted targets were examined through loss of miR-137 function experiments in rat cortical neurons. Finally, we conducted bioinformatics and literature analyses to examine the targets that were upregulated upon miR-137 downregulation. Results:Predicted human and mouse miR-137 targets were enriched in neuronal processes, such as axon guidance, neuritogenesis and neurotransmission. The miR-137 levels were significantly downregulated after EE, and we identified 5 novel miR-137 targets through loss of miR-137 function experiments. These targets fit into a glucocorticoid receptor-dependent signalling network that also includes 3 known miR-137 targets with genome-wide significant association with schizophrenia. Limitations:The bioinformatics analyses involved predicted human and mouse miR-137 targets owing to lack of information on predicted rat miR-137 targets, whereas follow-up experiments were performed with rats. Furthermore, indirect effects in the loss of miR-137 function experiments cannot be excluded. Conclusion:We have identified a miR-137-regulated protein network that contributes to our understanding of the molecular basis of schizophrenia and provides clues for future research into psychopharmacological treatments for schizophrenia.
机译:背景:精神分裂症是一种高度可遗传的神经发育障碍。 microRNA-137(miR-137)的遗传变异已产生与精神分裂症的全基因组关联,这表明该miRNA在其病因中起关键作用。因此,相互作用的miR-137靶标的分子网络可以提供对精神分裂症潜在生物学过程的见解。方法:我们首先使用生物信息学工具来获取和分析预测的人类和小鼠miR-137目标。然后,我们确定了环境富集(EE)后的大鼠桶状皮层中miR-137的水平,这是一种神经元可塑性模型,可诱导几个预测的miR-137靶标上调。随后,通过丧失大鼠皮质神经元中的miR-137功能实验来检查这些预测靶标的表达变化。最后,我们进行了生物信息学和文献分析,以检查在miR-137下调后上调的靶标。结果:预测的人和小鼠miR-137靶点在神经元过程中富集,例如轴突引导,神经形成和神经传递。 EE后,miR-137水平显着下调,并且我们通过丧失miR-137功能实验鉴定了5个新的miR-137目标。这些靶标适合糖皮质激素受体依赖性信号传导网络,该网络还包括3个已知的miR-137靶标,与精神分裂症在全基因组范围内具有显着关联。局限性:由于缺乏关于预测的大鼠miR-137靶标的信息,生物信息学分析涉及预测的人类和小鼠miR-137靶标,而对大鼠进行了后续实验。此外,不能排除miR-137功能丧失实验中的间接影响。结论:我们已经确定了miR-137调控的蛋白质网络,有助于我们对精神分裂症的分子基础的了解,并为精神分裂症的心理药物治疗的未来研究提供了线索。

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