错位进食使棕色脂肪组织内部和外周时钟之间的日节律失衡。

IF 7.5 1区 生物学 Q1 CELL BIOLOGY Cell reports Pub Date : 2024-08-27 Epub Date: 2024-07-23 DOI:10.1016/j.celrep.2024.114523
Victoria A Acosta-Rodríguez, Filipa Rijo-Ferreira, Laura van Rosmalen, Mariko Izumo, Noheon Park, Chryshanthi Joseph, Chelsea Hepler, Anneke K Thorne, Jeremy Stubblefield, Joseph Bass, Carla B Green, Joseph S Takahashi
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引用次数: 0

摘要

在休息期间长时间进食会扰乱外周和大脑昼夜节律钟之间的相位关系,从而对健康产生不利影响。除了肝脏之外,代谢器官如何对定时低热量饮食做出反应在很大程度上还没有被研究。与肝脏和下丘脑相比,我们研究了进食时间如何影响附睾白色和棕色脂肪组织(eWAT和BAT)的昼夜节律基因表达。我们限制C57BL/6J雄性小鼠白天或夜间进食,同时限制或不限制热量。与肝脏和eWAT不同,BAT中的节律性时钟基因仍然对进食时间不敏感,这一点与下丘脑类似。我们发现,在对相互冲突的环境线索做出反应时,BAT内部出现了分裂,在不改变其局部核心昼夜节律机制的情况下,一组代谢基因出现了反向振荡。将特定组织对昼夜节律转录网络的反应与代谢结果结合起来,可能有助于阐明在非正常时间进食对健康造成负担的机制。
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Misaligned feeding uncouples daily rhythms within brown adipose tissue and between peripheral clocks.

Extended food consumption during the rest period perturbs the phase relationship between circadian clocks in the periphery and the brain, leading to adverse health effects. Beyond the liver, how metabolic organs respond to a timed hypocaloric diet is largely unexplored. We investigated how feeding schedules impacted circadian gene expression in epididymal white and brown adipose tissue (eWAT and BAT) compared to the liver and hypothalamus. We restricted food to either daytime or nighttime in C57BL/6J male mice, with or without caloric restriction. Unlike the liver and eWAT, rhythmic clock genes in the BAT remained insensitive to feeding time, similar to the hypothalamus. We uncovered an internal split within the BAT in response to conflicting environmental cues, displaying inverted oscillations on a subset of metabolic genes without modifying its local core circadian machinery. Integrating tissue-specific responses on circadian transcriptional networks with metabolic outcomes may help elucidate the mechanism underlying the health burden of eating at unusual times.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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