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昼夜节律钟:从干细胞到组织内稳态和再生。

Circadian clocks: from stem cells to tissue homeostasis and regeneration.

机构信息

Hubrecht Institute-KNAW and University Medical Center, Utrecht, The Netherlands

Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

EMBO Rep. 2018 Jan;19(1):18-28. doi: 10.15252/embr.201745130. Epub 2017 Dec 19.

Abstract

The circadian clock is an evolutionarily conserved timekeeper that adapts body physiology to diurnal cycles of around 24 h by influencing a wide variety of processes such as sleep-to-wake transitions, feeding and fasting patterns, body temperature, and hormone regulation. The molecular clock machinery comprises a pathway that is driven by rhythmic docking of the transcription factors BMAL1 and CLOCK on clock-controlled output genes, which results in tissue-specific oscillatory gene expression programs. Genetic as well as environmental perturbation of the circadian clock has been implicated in various diseases ranging from sleep to metabolic disorders and cancer development. Here, we review the origination of circadian rhythms in stem cells and their function in differentiated cells and organs. We describe how clocks influence stem cell maintenance and organ physiology, as well as how rhythmicity affects lineage commitment, tissue regeneration, and aging.

摘要

生物钟是一种进化上保守的计时器,通过影响广泛的过程,如睡眠-觉醒转换、进食和禁食模式、体温和激素调节,使身体生理适应大约 24 小时的昼夜节律。分子钟机制由转录因子 BMAL1 和 CLOCK 节律性地与时钟控制的输出基因结合驱动,导致组织特异性的振荡基因表达程序。生物钟的遗传和环境扰动与各种疾病有关,从睡眠到代谢紊乱和癌症发展。在这里,我们回顾了干细胞中昼夜节律的起源及其在分化细胞和器官中的功能。我们描述了时钟如何影响干细胞的维持和器官的生理机能,以及节律性如何影响谱系承诺、组织再生和衰老。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3423/5757216/7074127a394f/EMBR-19-18-g001.jpg

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