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Global analysis of gene expression mediated by OX1 orexin receptor signaling in a hypothalamic cell line

机译:OX1 orexin受体信号传导介导的下丘脑细胞系中基因表达的整体分析

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摘要

The orexins and their cognate G-protein coupled receptors have been widely studied due to their associations with various behaviors and cellular processes. However, the detailed downstream signaling cascades that mediate these effects are not completely understood. We report the generation of a neuronal model cell line that stably expresses the OX1 orexin receptor (OX1) and an RNA-Seq analysis of changes in gene expression seen upon receptor activation. Upon treatment with orexin, several families of related transcription factors are transcriptionally regulated, including the early growth response genes (Egr), the Kruppel-like factors (Klf), and the Nr4a subgroup of nuclear hormone receptors. Furthermore, some of the transcriptional effects observed have also been seen in data from in vivo sleep deprivation microarray studies, supporting the physiological relevance of the data set. Additionally, inhibition of one of the most highly regulated genes, serum and glucocorticoid-regulated kinase 1 (Sgk1), resulted in the diminished orexin-dependent induction of a subset of genes. These results provide new insight into the molecular signaling events that occur during OX1 signaling and support a role for orexin signaling in the stimulation of wakefulness during sleep deprivation studies.
机译:由于其与各种行为和细胞过程的联系,食欲素及其同源G蛋白偶联受体已被广泛研究。但是,尚未完全了解介导这些作用的详细下游信号传导级联。我们报告稳定表达OX1 orexin受体(OX1)的神经元模型细胞系的生成和受体激活后看到的基因表达变化的RNA-Seq分析。用orexin治疗后,相关转录因子的几个家族被转录调节,包括早期生长反应基因(Egr),Kruppel样因子(Klf)和核激素受体的Nr4a亚组。此外,在体内睡眠剥夺微阵列研究的数据中也观察到了一些转录效应,支持了该数据集的生理相关性。此外,抑制最严格的基因之一,血清和糖皮质激素调节激酶1(Sgk1),导致减少了orexin依赖的基因子集的诱导。这些结果提供了对在OX1信号转导期间发生的分子信号转导事件的新见解,并支持了orexin信号转导在睡眠剥夺研究中刺激觉醒的作用。

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