Circadian clocks: from stem cells to tissue homeostasis and regeneration

被引:89
作者
Dierickx, Pieterjan [1 ,2 ,6 ]
Van Laake, Linda W. [3 ,4 ]
Geijsen, Niels [1 ,2 ,5 ]
机构
[1] KNAW, Hubrecht Inst, Utrecht, Netherlands
[2] Univ Med Ctr, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Cardiol, Div Heart & Lungs, Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Regenerat Med Ctr Utrecht, Utrecht, Netherlands
[5] Univ Utrecht, Fac Vet Med Clin Sci Compan Anim, Utrecht, Netherlands
[6] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
关键词
aging; circadian rhythms; clock; regeneration; stem cells; REV-ERB; MOLECULAR CLOCK; GENE-EXPRESSION; INFARCT SIZE; DNA-DAMAGE; TRANSCRIPTION; RHYTHMS; DIFFERENTIATION; METABOLISM; COMPONENT;
D O I
10.15252/embr.201745130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:18 / 28
页数:11
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