Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study

睡眠剥夺 蛋白质组学 脑脊液 清醒 睡眠(系统调用) 炎症 下调和上调 信号转导 生物 生物途径 免疫系统 医学 生物信息学 神经科学 细胞生物学 免疫学 基因 生物化学 基因表达 昼夜节律 脑电图 操作系统 计算机科学
作者
Ana del C. Vaquer-Alicea,Jinsheng Yu,Haiyan Liu,Brendan P. Lucey
出处
期刊:Sleep advances [Oxford University Press]
卷期号:4 (1) 被引量:3
标识
DOI:10.1093/sleepadvances/zpad047
摘要

Abstract Study Objectives Acute sleep deprivation affects both central and peripheral biological processes. Prior research has mainly focused on specific proteins or biological pathways that are dysregulated in the setting of sustained wakefulness. This exploratory study aimed to provide a comprehensive view of the biological processes and proteins impacted by acute sleep deprivation in both plasma and cerebrospinal fluid (CSF). Methods We collected plasma and CSF from human participants during one night of sleep deprivation and controlled normal sleep conditions. One thousand and three hundred proteins were measured at hour 0 and hour 24 using a high-scale aptamer-based proteomics platform (SOMAscan) and a systematic biological database tool (Metascape) was used to reveal altered biological pathways. Results Acute sleep deprivation decreased the number of upregulated and downregulated biological pathways and proteins in plasma but increased upregulated and downregulated biological pathways and proteins in CSF. Predominantly affected proteins and pathways were associated with immune response, inflammation, phosphorylation, membrane signaling, cell-cell adhesion, and extracellular matrix organization. Conclusions The identified modifications across biofluids add to evidence that acute sleep deprivation has important impacts on biological pathways and proteins that can negatively affect human health. As a hypothesis-driving study, these findings may help with the exploration of novel mechanisms that mediate sleep loss and associated conditions, drive the discovery of new sleep loss biomarkers, and ultimately aid in the identification of new targets for intervention to human diseases.

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