Koesema Eric, Kodadek Thomas
Department of Chemistry, The Scripps Research Institute, Scripps Florida, Jupiter, FL, United States of America.
PLoS One. 2017 Nov 16;12(11):e0188082. doi: 10.1371/journal.pone.0188082. eCollection 2017.
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.
食欲素及其同源G蛋白偶联受体因其与各种行为和细胞过程的关联而受到广泛研究。然而,介导这些效应的详细下游信号级联尚未完全清楚。我们报告了一种稳定表达OX1食欲素受体(OX1)的神经元模型细胞系的产生,以及对受体激活后基因表达变化的RNA测序分析。用食欲素处理后,几个相关转录因子家族受到转录调控,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,这支持了该数据集的生理相关性。此外,抑制调控程度最高的基因之一血清和糖皮质激素调节激酶1(Sgk1),会导致食欲素依赖性的一部分基因诱导作用减弱。这些结果为OX1信号传导过程中发生的分子信号事件提供了新的见解,并支持食欲素信号在睡眠剥夺研究中刺激清醒方面的作用。