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It’s about time: clocks in the developing lung
Colleen M. Bartman, Aleksey Matveyenko, Y.S. Prakash
Colleen M. Bartman, Aleksey Matveyenko, Y.S. Prakash
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Review

It’s about time: clocks in the developing lung

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Abstract

The discovery of peripheral intracellular clocks revealed circadian oscillations of clock genes and their targets in all cell types, including those in the lung, sparking exploration of clocks in lung disease pathophysiology. While the focus has been on the role of these clocks in adult airway diseases, clock biology is also likely to be important in perinatal lung development, where it has received far less attention. Historically, fetal circadian rhythms have been considered irrelevant owing to lack of external light exposure, but more recent insights into peripheral clock biology raise questions of clock emergence, its concordance with tissue-specific structure/function, the interdependence of clock synchrony and functionality in perinatal lung development, and the possibility of lung clocks in priming the fetus for postnatal life. Understanding the perinatal molecular clock may unravel mechanistic targets for chronic airway disease across the lifespan. With current research providing more questions than answers, it is about time to investigate clocks in the developing lung.

Authors

Colleen M. Bartman, Aleksey Matveyenko, Y.S. Prakash

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Figure 3

Leveraging LungMAP for a glimpse into lung clocks.

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Leveraging LungMAP for a glimpse into lung clocks.
Data from the Nationa...
Data from the National Heart, Lung, and Blood Institute’s LungMAP consortium (www.lungmap.net) provide glimpses into the spatial and temporal dynamism of clock gene expression in the postnatal human lung, a more relevant time period in the context of healthy growth and perinatal/pediatric disease. Clock genes such as PER1 appear to be substantially expressed in the early postnatal period, while showing considerable variation in different lung cell types toward adulthood. Genes such as PER1 could be appealing to explore in the context of lung growth, responses to insults like oxygen or inflammation in prematurity, and initiation of chronic lung diseases. It may also be important to consider whether differential expression in epithelial versus mesenchymal cells is relevant to specific disease progression.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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