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跨物种研究人类和果蝇发现睡眠缺失的标志物。

Cross-translational studies in human and Drosophila identify markers of sleep loss.

机构信息

Department of Anatomy and Physiology, Washington University School of Medicine, St. Louis, Missouri, United States of America.

出版信息

PLoS One. 2013 Apr 24;8(4):e61016. doi: 10.1371/journal.pone.0061016. Print 2013.

Abstract

Inadequate sleep has become endemic, which imposes a substantial burden for public health and safety. At present, there are no objective tests to determine if an individual has gone without sleep for an extended period of time. Here we describe a novel approach that takes advantage of the evolutionary conservation of sleep to identify markers of sleep loss. To begin, we demonstrate that IL-6 is increased in rats following chronic total sleep deprivation and in humans following 30 h of waking. Discovery experiments were then conducted on saliva taken from sleep-deprived human subjects to identify candidate markers. Given the relationship between sleep and immunity, we used Human Inflammation Low Density Arrays to screen saliva for novel markers of sleep deprivation. Integrin αM (ITGAM) and Anaxin A3 (AnxA3) were significantly elevated following 30 h of sleep loss. To confirm these results, we used QPCR to evaluate ITGAM and AnxA3 in independent samples collected after 24 h of waking; both transcripts were increased. The behavior of these markers was then evaluated further using the power of Drosophila genetics as a cost-effective means to determine whether the marker is associated with vulnerability to sleep loss or other confounding factors (e.g., stress). Transcript profiling in flies indicated that the Drosophila homologues of ITGAM were not predictive of sleep loss. Thus, we examined transcript levels of additional members of the integrin family in flies. Only transcript levels of scab, the Drosophila homologue of Integrin α5 (ITGA5), were associated with vulnerability to extended waking. Since ITGA5 was not included on the Low Density Array, we returned to human samples and found that ITGA5 transcript levels were increased following sleep deprivation. These cross-translational data indicate that fly and human discovery experiments are mutually reinforcing and can be used interchangeably to identify candidate biomarkers of sleep loss.

摘要

睡眠不足已成为普遍现象,这给公共卫生和安全带来了巨大负担。目前,尚无客观测试来确定个体是否长时间没有睡眠。在这里,我们描述了一种新颖的方法,该方法利用睡眠的进化保守性来识别睡眠不足的标志物。首先,我们证明慢性完全睡眠剥夺后大鼠的白细胞介素 6(IL-6)增加,并且 30 小时清醒后人类的白细胞介素 6(IL-6)增加。然后,在睡眠剥夺的人类受试者的唾液中进行了发现实验,以鉴定候选标志物。鉴于睡眠与免疫之间的关系,我们使用人类炎症低密度阵列筛选唾液中睡眠剥夺的新型标志物。整合素 αM(ITGAM)和膜联蛋白 A3(AnxA3)在 30 小时睡眠剥夺后显着升高。为了确认这些结果,我们使用 QPCR 在 24 小时清醒后收集的独立样本中评估 ITGAM 和 AnxA3;两种转录物均增加。然后,使用 Drosophila 遗传学的强大功能进一步评估这些标志物的行为,这是一种经济有效的方法,可以确定标志物是否与对睡眠剥夺或其他混杂因素(例如压力)的易感性有关。苍蝇中的转录谱分析表明,ITGAM 的果蝇同源物不能预测睡眠剥夺。因此,我们检查了苍蝇中整合素家族其他成员的转录物水平。只有 scab(果蝇同源物 Integrin α5(ITGA5))的转录物水平与延长清醒的易感性有关。由于 ITGA5 未包含在低密度阵列中,因此我们返回人类样本并发现睡眠剥夺后 ITGA5 转录物水平增加。这些跨翻译数据表明,苍蝇和人类的发现实验是相互加强的,可以互换使用以鉴定睡眠剥夺的候选生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9c/3634862/ceba552ff255/pone.0061016.g001.jpg

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