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肝代谢循环的时相分隔逻辑。

Logic of the Temporal Compartmentalization of the Hepatic Metabolic Cycle.

机构信息

Aging Institute of UPMC, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

Pittsburgh Liver Research Center, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

Physiology (Bethesda). 2022 Sep 1;37(5):0. doi: 10.1152/physiol.00003.2022. Epub 2022 Jun 6.

DOI:10.1152/physiol.00003.2022
PMID:35658626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9394779/
Abstract

The mammalian liver must cope with various metabolic and physiological changes that normally recur every day and result primarily from rest-activity and fasting-feeding cycles. In this article, I present evidence supporting a temporal compartmentalization of rhythmic hepatic metabolic processes into four main clusters: regulation of energy homeostasis, maintenance of information integrity, immune response, and genetic information flow. I further review literatures and discuss how both the circadian and the newly discovered 12-h ultradian clock work together to regulate these four temporally separated processes in mouse liver, which, interestingly, is largely uncoupled from the liver zonation regulation.

摘要

哺乳动物的肝脏必须应对各种代谢和生理变化,这些变化通常每天都会重复发生,主要源于休息-活动和禁食-进食循环。在本文中,我提出了证据支持将节律性肝代谢过程按时间分隔成四个主要簇:能量稳态的调节、信息完整性的维持、免疫反应和遗传信息流。我进一步回顾了文献,并讨论了昼夜节律和新发现的 12 小时超昼夜节律如何共同调节小鼠肝脏中的这四个时间分离的过程,有趣的是,这与肝脏分区调节在很大程度上是解耦的。

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2
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本文引用的文献

1
Defining the mammalian coactivation of hepatic 12-h clock and lipid metabolism.定义哺乳动物肝脏 12 小时时钟和脂质代谢的共激活作用。
Cell Rep. 2022 Mar 8;38(10):110491. doi: 10.1016/j.celrep.2022.110491.
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Mutation bias reflects natural selection in Arabidopsis thaliana.突变偏向反映了拟南芥中的自然选择。
Nature. 2022 Feb;602(7895):101-105. doi: 10.1038/s41586-021-04269-6. Epub 2022 Jan 12.
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Four-dimensional nuclear speckle phase separation dynamics regulate proteostasis.四维核斑点相分离动力学调节蛋白质稳态。
Sci Adv. 2022 Jan 7;8(1):eabl4150. doi: 10.1126/sciadv.abl4150. Epub 2022 Jan 5.
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Reciprocal regulation of chaperone-mediated autophagy and the circadian clock.伴侣蛋白介导的自噬与生物钟的相互调节。
Nat Cell Biol. 2021 Dec;23(12):1255-1270. doi: 10.1038/s41556-021-00800-z. Epub 2021 Dec 7.
5
NF-κB modifies the mammalian circadian clock through interaction with the core clock protein BMAL1.核因子-κB通过与核心生物钟蛋白BMAL1相互作用来调节哺乳动物的生物钟。
PLoS Genet. 2021 Nov 22;17(11):e1009933. doi: 10.1371/journal.pgen.1009933. eCollection 2021 Nov.
6
Autonomous clocks that regulate organelle biogenesis, cytoskeletal organization, and intracellular dynamics.自主时钟调节细胞器生物发生、细胞骨架组织和细胞内动力学。
Elife. 2021 Sep 29;10:e72104. doi: 10.7554/eLife.72104.
7
Feeding-induced resistance to acute lethal sepsis is dependent on hepatic BMAL1 and FXR signalling.摄食诱导的急性致死性脓毒症抵抗依赖于肝脏 BMAL1 和 FXR 信号转导。
Nat Commun. 2021 May 12;12(1):2745. doi: 10.1038/s41467-021-22961-z.
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Revealing the hidden reality of the mammalian 12-h ultradian rhythms.揭示哺乳动物 12 小时超日节律的隐藏现实。
Cell Mol Life Sci. 2021 Apr;78(7):3127-3140. doi: 10.1007/s00018-020-03730-5. Epub 2021 Jan 15.
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Space-time logic of liver gene expression at sub-lobular scale.亚肝小叶尺度下肝脏基因表达的时空逻辑。
Nat Metab. 2021 Jan;3(1):43-58. doi: 10.1038/s42255-020-00323-1. Epub 2021 Jan 11.
10
Clocks, cancer, and chronochemotherapy.时钟、癌症与时间化疗。
Science. 2021 Jan 1;371(6524). doi: 10.1126/science.abb0738.