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Mucosal Immunol ; 11(1): 97-111, 2018 01.
Artículo en Inglés | MEDLINE | ID: mdl-28401936

RESUMEN

Patients with asthma experience circadian variations in their symptoms. However it remains unclear how specific aspects of this common airway disease relate to clock genes, which are critical to the generation of circadian rhythms in mammals. Here, we used a viral model of acute and chronic airway disease to examine how circadian clock disruption affects asthmatic lung phenotypes. Deletion of the core clock gene bmal1 or environmental disruption of circadian function by jet lag exacerbated acute viral bronchiolitis caused by Sendai virus (SeV) and influenza A virus in mice. Post-natal deletion of bmal1 was sufficient to trigger increased SeV susceptibility and correlated with impaired control of viral replication. Importantly, bmal1-/- mice developed much more extensive asthma-like airway changes post infection, including mucus production and increased airway resistance. In human airway samples from two asthma cohorts, we observed altered expression patterns of multiple clock genes. Our results suggest a role for bmal1 in the development of asthmatic airway disease via the regulation of lung antiviral responses to common viral triggers of asthma.


Asunto(s)
Factores de Transcripción ARNTL/genética , Asma/inmunología , Bronquiolitis Viral/inmunología , Relojes Circadianos/genética , Virus de la Influenza A/fisiología , Infecciones por Orthomyxoviridae/inmunología , Infecciones por Respirovirus/inmunología , Virus Sendai/inmunología , Factores de Transcripción ARNTL/metabolismo , Remodelación de las Vías Aéreas (Respiratorias)/genética , Resistencia de las Vías Respiratorias/genética , Animales , Estudios de Cohortes , Modelos Animales de Enfermedad , Humanos , Ratones , Ratones Noqueados , Moco/metabolismo , Replicación Viral
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