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Published on: April 13, 2015
Time-of-Day-Dependent Trafficking and Function of Leukocyte Subsets
Robert Pick1, Wenyan He2, Chien-Sin Chen3
1Walter-Brendel-Centre of Experimental Medicine, University Hospital, Ludwig-Maximilians-University Munich, BioMedical Centre, Planegg-Martinsried, Germany; These authors contributed equally to this work.
Insights
Mammalian blood leukocyte counts follow a daily circadian rhythm. This study details how rhythmic expression of molecules controls leukocyte movement into tissues, offering potential therapeutic strategies.
Area of Science:
- Immunology
- Chronobiology
- Cell Biology
Background:
- Circadian rhythms influence physiological processes, including immune cell circulation.
- Leukocyte migration is critical for immune surveillance and inflammatory responses.
Purpose of the Study:
- To summarize recent findings on the mechanisms of circadian-controlled leukocyte migration.
- To highlight molecular regulators of rhythmic leukocyte recruitment.
- To explore the role of clock genes in leukocyte function and migration.
Main Methods:
- Review of latest research findings on leukocyte migration and circadian control.
- Analysis of molecular mechanisms involving adhesion molecules, chemokines, and receptors.
- Comparison of immune cell rhythms in steady-state, inflammation, and disease.
Main Results:
- Leukocyte migration into organs is under circadian control, involving specific molecules.
- Oscillatory expression of adhesion molecules, chemokines, and receptors governs rhythmic leukocyte recruitment.
- Clock genes are relevant for leukocyte function and migration patterns.
Conclusions:
- Circadian regulation of leukocyte migration is mediated by rhythmic molecular interactions.
- Understanding these rhythms offers potential for novel therapeutic interventions in immune-related conditions.
- Immune cell rhythms differ between homeostatic and disease states.
Abstract:
The number of leukocytes circulating in blood in mammals is under circadian control (i.e., ∼24h). We summarize here latest findings on the mechanisms governing leukocyte migration from the blood into various organs, focusing on the distinct leukocyte subtype- and tissue-specific molecules involved. We highlight the oscillatory expression patterns of adhesion molecules, chemokines, and their receptors that are expressed on endothelial cells and leukocytes, and which are crucial regulators of rhythmic leukocyte recruitment. We also discuss the relevance of clock genes for leukocyte function and migration. Finally, we compare immune cell rhythms under steady-state conditions as well as during inflammation and disease, and we postulate how these findings provide potential new avenues for therapeutic intervention.
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