Computational modeling of the synergistic role of GCN2 and the HPA axis in regulating the integrated stress response in the central circadian timing system.

IF 2.5 4区 生物学 Q3 CELL BIOLOGY Physiological genomics Pub Date : 2024-08-01 Epub Date: 2024-06-17 DOI:10.1152/physiolgenomics.00030.2024
Yannuo Li, Lingjun Lu, Jordan L Levy, Tracy G Anthony, Ioannis P Androulakis
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Abstract

The circadian timing system and integrated stress response (ISR) systems are fundamental regulatory mechanisms that maintain body homeostasis. The central circadian pacemaker in the suprachiasmatic nucleus (SCN) governs daily rhythms through interactions with peripheral oscillators via the hypothalamus-pituitary-adrenal (HPA) axis. On the other hand, ISR signaling is pivotal for preserving cellular homeostasis in response to physiological changes. Notably, disrupted circadian rhythms are observed in cases of impaired ISR signaling. In this work, we examine the potential interplay between the central circadian system and the ISR, mainly through the SCN and HPA axis. We introduce a semimechanistic mathematical model to delineate SCN's capacity for indirectly perceiving physiological stress through glucocorticoid-mediated feedback from the HPA axis and orchestrating a cellular response via the ISR mechanism. Key components of our investigation include evaluating general control nonderepressible 2 (GCN2) expression in the SCN, the effect of physiological stress stimuli on the HPA axis, and the interconnected feedback between the HPA and SCN. Simulation revealed a critical role for GCN2 in linking ISR with circadian rhythms. Experimental findings have demonstrated that a Gcn2 deletion in mice leads to rapid re-entrainment of the circadian clock following jetlag as well as to an elongation of the circadian period. These phenomena are well replicated by our model, which suggests that both the swift re-entrainment and prolonged period can be ascribed to a reduced robustness in neuronal oscillators. Our model also offers insights into phase shifts induced by acute physiological stress and the alignment/misalignment of physiological stress with external light-dark cues. Such understanding aids in strategizing responses to stressful events, such as nutritional status changes and jetlag.NEW & NOTEWORTHY This study is the first theoretical work to investigate the complex interaction between integrated stress response (ISR) sensing and central circadian rhythm regulation, encompassing the suprachiasmatic nucleus (SCN) and hypothalamus-pituitary-adrenal (HPA) axis. The findings carry implications for the development of dietary or pharmacological interventions aimed at facilitating recovery from stressful events, such as jetlag. Moreover, they provide promising prospects for potential therapeutic interventions that target circadian rhythm disruption and various stress-related disorders.

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关于 GCN2 和 HPA 轴在调节中枢昼夜节律定时系统综合压力反应中的协同作用的计算模型。
昼夜节律定时系统和综合应激反应(ISR)系统是维持机体平衡的基本调节机制。位于嗜铬细胞上核(SCN)的中枢昼夜节律起搏器通过下丘脑-垂体-肾上腺(HPA)轴与外周振荡器相互作用,控制着每日的节律。另一方面,ISR 信号对于维持细胞平衡以应对生理变化至关重要。值得注意的是,在 ISR 信号受损的情况下会出现昼夜节律紊乱。在这项工作中,我们研究了中枢昼夜节律系统和 ISR 之间的潜在相互作用,主要是通过 SCN 和 HPA 轴。我们引入了一个半机制数学模型,以描述嗜铬细胞上核(SCN)通过糖皮质激素介导的 HPA 轴反馈间接感知生理压力并通过 ISR 机制协调细胞反应的能力。我们研究的主要内容包括评估 SCN 中一般控制不可解压 2(GCN2)的表达、生理压力刺激对 HPA 轴的影响以及 HPA 和 SCN 之间相互关联的反馈。模拟揭示了 GCN2 在连接 ISR 与昼夜节律中的关键作用。实验结果表明,在小鼠体内缺失 Gcn2 会导致昼夜节律时钟在时差之后迅速重新调整,并导致昼夜节律周期延长。这些
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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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