Circadian rhythm reprogramming during lung inflammation Academic Article uri icon

Overview

MeSH Major

  • CLOCK Proteins
  • Circadian Rhythm
  • Lung
  • Pneumonia
  • RNA, Messenger

abstract

  • Circadian rhythms are known to regulate immune responses in healthy animals, but it is unclear whether they persist during acute illnesses where clock gene expression is disrupted by systemic inflammation. Here we use a genome-wide approach to investigate circadian gene and metabolite expression in the lungs of endotoxemic mice and find that novel cellular and molecular circadian rhythms are elicited in this setting. The endotoxin-specific circadian programme exhibits unique features, including a divergent group of rhythmic genes and metabolites compared with the basal state and a distinct periodicity and phase distribution. At the cellular level, endotoxin treatment also alters circadian rhythms of leukocyte counts within the lung in a bmal1-dependent manner, such that granulocytes rather than lymphocytes become the dominant oscillating cell type. Our results show that inflammation produces a complex re-organization of cellular and molecular circadian rhythms that are relevant to early events in lung injury.

publication date

  • September 11, 2014

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC4162491

Digital Object Identifier (DOI)

  • 10.1038/ncomms5753

PubMed ID

  • 25208554

Additional Document Info

start page

  • 4753

volume

  • 5