期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 117, 期 1, 页码 779-786出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1914112117
关键词
circadian clock; metabolism; hypoxia; PER2::LUC mice; obstructive sleep apnea
资金
- European Research Council (ERC-2017 CIRCOMMUNICATION) [770869]
- Abisch Frenkel Foundation for the Promotion of Life Sciences
- Adelis Foundation
- EMBO Young Investigator award
- Azrieli Foundation
- European Research Council (ERC) [770869] Funding Source: European Research Council (ERC)
The occurrence and sequelae of disorders that lead to hypoxic spells such as asthma, chronic obstructive pulmonary disease, and obstructive sleep apnea (OSA) exhibit daily variance. This prompted us to examine the interaction between the hypoxic response and the circadian clock in vivo. We found that the global transcriptional response to acute hypoxia is tissue-specific and time-of-day-dependent. In particular, clock components differentially responded at the transcriptional and posttranscriptional level, and these responses depended on an intact circadian clock. Importantly, exposure to hypoxia phase-shifted clocks in a tissue-dependent manner led to intertissue circadian clock misalignment. This differential response relied on the intrinsic properties of each tissue and could be recapitulated ex vivo. Notably, circadian misalignment was also elicited by intermittent hypoxia, a widely used model for OSA. Given that phase coherence between circadian clocks is considered favorable, we propose that hypoxia leads to circadian misalignment, contributing to the pathophysiology of OSA and potentially other diseases that involve hypoxia.
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