Circadian asthma airway responses are gated by REV-ERBα

被引:34
作者
Durrington, Hannah J.
Krakowiak, Karolina
Meijer, Peter
Begley, Nicola
Maidstone, Robert
Goosey, Laurence
Gibbs, Julie E.
Blaikley, John F.
Gregory, Lisa G.
Lloyd, Clare M.
Loudon, Andrew S., I
Ray, David W.
机构
[1] Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester
[2] Wythenshawe Hospital, University Hospital of South Manchester, Manchester University NHS Foundation Trust (MFT), Manchester
[3] Division of Diabetes, Endocrinology and Gastroenterology, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester
[4] Division of Informatics, Imaging and Data Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester
[5] National Heart and Lung Institute, Imperial College, London
[6] NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford
[7] Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford
基金
英国惠康基金; 英国医学研究理事会;
关键词
BRONCHIAL RESPONSIVENESS; PULMONARY INFLAMMATION; HOUSE-DUST; CLOCK; HYPERRESPONSIVENESS; HYPERREACTIVITY; RHYTHM;
D O I
10.1183/13993003.02407-2019
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: The circadian clock powerfully regulates inflammation and the clock protein REV-ERB alpha is known to play a key role as a repressor of the inflammatory response. Asthma is an inflammatory disease of the airways with a strong time of day rhythm. Airway hyper-responsiveness (AHR) is a dominant feature of asthma; however, it is not known if this is under clock control. Objectives: To determine if allergy-mediated AHR is gated by the clock protein REV-ERB alpha. Methods: After exposure to the intra-nasal house dust mite (HDM) allergen challenge model at either dawn or dusk, AHR to methacholine was measured invasively in mice. Main results: Wild-type (WT) mice show markedly different time of day AHR responses (maximal at dusk/start of the active phase), both in vivo and ex vivo, in precision cut lung slices. Time of day effects on AHR were abolished in mice lacking the clock gene Rev-erb alpha, indicating that such effects on asthma response are likely to be mediated via the circadian clock. We suggest that muscarinic receptors one (Chrm 1) and three (Chrm 3) may play a role in this pathway. Conclusions: We identify a novel circuit regulating a core process in asthma, potentially involving circadian control of muscarinic receptor expression, in a REV-ERB alpha dependent fashion. Clinical implication: These insights suggest the importance of considering the timing of drug administration in clinic trials and in clinical practice (chronotherapy).
引用
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页数:13
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