Department of Biomolecular Sciences, Weizmann Institute of Science, 7610001 Rehovot, Israel.
School of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol BS8 1TH, UK.
Cell Metab. 2017 Jan 10;25(1):93-101. doi: 10.1016/j.cmet.2016.09.014. Epub 2016 Oct 20.
The mammalian circadian system consists of a master clock in the brain that synchronizes subsidiary oscillators in peripheral tissues. The master clock maintains phase coherence in peripheral cells through systemic cues such as feeding-fasting and temperature cycles. Here, we examined the role of oxygen as a resetting cue for circadian clocks. We continuously measured oxygen levels in living animals and detected daily rhythms in tissue oxygenation. Oxygen cycles, within the physiological range, were sufficient to synchronize cellular clocks in a HIF1α-dependent manner. Furthermore, several clock genes responded to changes in oxygen levels through HIF1α. Finally, we found that a moderate reduction in oxygen levels for a short period accelerates the adaptation of wild-type but not of HIF1α-deficient mice to the new time in a jet lag protocol. We conclude that oxygen, via HIF1α activation, is a resetting cue for circadian clocks and propose oxygen modulation as therapy for jet lag.
哺乳动物的生物钟系统由大脑中的主钟控制,主钟通过系统提示(如进食-禁食和温度循环)来同步外周组织中的附属振荡器。主钟通过系统提示(如进食-禁食和温度循环)来保持外周细胞的相位一致性。在这里,我们研究了氧气作为生物钟重置提示的作用。我们连续测量了活体动物的氧气水平,并检测到组织氧合的日常节律。在生理范围内的氧气循环足以通过 HIF1α 以依赖的方式同步细胞时钟。此外,通过 HIF1α,几个时钟基因对氧气水平的变化做出反应。最后,我们发现,短暂的适度降低氧气水平可以加速野生型小鼠而不是 HIF1α 缺陷型小鼠适应新的时差,在时差调整方案中。我们的结论是,氧气通过 HIF1α 激活是生物钟的重置提示,我们提出通过氧气调节作为时差调整的治疗方法。