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Gut microbiota directs PPARγ‐driven reprogramming of the liver circadian clock by nutritional challenge

机译:肠道菌群通过营养挑战指导肝脏昼夜节律钟的PPARγ驱动重编程

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摘要

The liver circadian clock is reprogrammed by nutritional challenge through the rewiring of specific transcriptional pathways. As the gut microbiota is tightly connected to host metabolism, whose coordination is governed by the circadian clock, we explored whether gut microbes influence circadian homeostasis and how they distally control the peripheral clock in the liver. Using fecal transplant procedures we reveal that, in response to high‐fat diet, the gut microbiota drives PPARγ‐mediated activation of newly oscillatory transcriptional programs in the liver. Moreover, antibiotics treatment prevents PPARγ‐driven transcription in the liver, underscoring the essential role of gut microbes in clock reprogramming and hepatic circadian homeostasis. Thus, a specific molecular signature characterizes the influence of the gut microbiome in the liver, leading to the transcriptional rewiring of hepatic metabolism.
机译:通过重新连接特定的转录途径,通过营养挑战对肝脏生物钟进行重新编程。由于肠道菌群与宿主代谢密切相关,宿主的协调性由昼夜节律控制,因此我们探讨了肠道微生物是否会影响昼夜节律,以及它们如何远端控制肝脏的外围时钟。使用粪便移植程序,我们发现,响应高脂饮食,肠道菌群会驱动PPARγ介导的肝脏新振荡转录程序的激活。此外,抗生素治疗可防止PPARγ驱动的肝脏转录,强调肠道微生物在时钟重编程和肝脏昼夜节律平衡中的重要作用。因此,特定的分子标记表征了肝脏中肠道微生物组的影响,从而导致肝代谢的转录重新连接。

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