External Cues as Transducers of Peripheral Tissue-Specific Molecular Clocks to Regulate Systemic Circadian Rhythms and Metabolism

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhe Zhang, Bei-bei Liu, Shu-zhe Ding
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Abstract

The molecular clock exhibits distinct characteristics across various tissues and can be synchronized by particular stimuli. Furthermore, there is an intricate interplay among the molecular clocks within different tissues. In this context, we present an overview of the tissue-specific molecular clock and discuss pivotal nonphotic regulators that govern the host's circadian rhythms and metabolic processes. Intermittent time-restricted feeding establishes rhythmicity and harmony in hepatic proteasome activity through various pathways and modulates hormone levels and lifespan extension via the synergistic action of molecular clocks and autophagy (AMPK, mTOR, SIRT1). High-fat diet (HFD) alters the molecular clock rhythms in the mediobasal hypothalamus (MBH), adipose tissue, and liver, with particularly pronounced changes observed in adipose tissue. HFD alters rhythm by inhibiting CLOCK:BMAL1 chromatin recruitment and activating the PPARγ pathway in the liver. The absence of liver CLOCK or intestinal BMAL1 mitigates metabolic disturbances, such as obesity, induced by long-term HFD. Meanwhile, intestinal microbiota also directly or indirectly regulates the host's circadian network and metabolism through micromolecules. Correspondingly, deletion of molecular clock genes alters the diurnal variations, composition, and function of the gut microbiome at the genus level in mice. The mechanisms underlying the tissue-specific effects of the gut microbiota on peripheral clocks are currently being unraveled and require further elucidation, with PPAR emerging as a pivotal factor in this process. The effect of exercise on the molecular clock of skeletal muscle varies depending on distinct muscle fiber types and the intensity of exercise. Identifying the optimal combination of chrono-exercise and intermittent fasting represents a substantial research opportunity. Additionally, the interplay between the molecular clocks of various tissues in response to specific rhythmic cues merits thorough investigation.

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外部信号作为外周组织特异性分子钟的转导来调节全身昼夜节律和代谢
分子钟在不同的组织中表现出不同的特征,可以通过特定的刺激来同步。此外,不同组织内的分子钟之间存在着复杂的相互作用。在此背景下,我们介绍了组织特异性分子钟的概述,并讨论了控制宿主昼夜节律和代谢过程的关键非光调节因子。间歇性限时饲喂通过多种途径使肝蛋白酶体活性具有节律性和协调性,并通过分子钟和自噬(AMPK, mTOR, SIRT1)的协同作用调节激素水平和延长寿命。高脂肪饮食(HFD)改变了中基底下丘脑(MBH)、脂肪组织和肝脏的分子时钟节律,在脂肪组织中观察到特别明显的变化。HFD通过抑制肝脏中CLOCK:BMAL1染色质募集和激活PPARγ通路来改变节律。肝脏CLOCK或肠道BMAL1的缺失减轻了由长期HFD引起的代谢紊乱,如肥胖。同时,肠道微生物群也通过微分子直接或间接调节宿主的昼夜节律网络和代谢。相应地,分子钟基因的缺失会在属水平上改变小鼠肠道微生物组的昼夜变化、组成和功能。肠道微生物群对外周时钟的组织特异性影响的机制目前正在解开,需要进一步阐明,PPAR在这一过程中成为关键因素。运动对骨骼肌分子钟的影响取决于不同的肌纤维类型和运动强度。确定计时运动和间歇性禁食的最佳组合是一个重要的研究机会。此外,各种组织的分子钟之间的相互作用,以响应特定的节奏线索值得深入研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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