Circadian Expression of Migratory Factors Establishes Lineage-Specific Signatures that Guide the Homing of Leukocyte Subsets to Tissues

Immunity. 2018 Dec 18;49(6):1175-1190.e7. doi: 10.1016/j.immuni.2018.10.007. Epub 2018 Dec 4.

Abstract

The number of leukocytes present in circulation varies throughout the day, reflecting bone marrow output and emigration from blood into tissues. Using an organism-wide circadian screening approach, we detected oscillations in pro-migratory factors that were distinct for specific vascular beds and individual leukocyte subsets. This rhythmic molecular signature governed time-of-day-dependent homing behavior of leukocyte subsets to specific organs. Ablation of BMAL1, a transcription factor central to circadian clock function, in endothelial cells or leukocyte subsets demonstrated that rhythmic recruitment is dependent on both microenvironmental and cell-autonomous oscillations. These oscillatory patterns defined leukocyte trafficking in both homeostasis and inflammation and determined detectable tumor burden in blood cancer models. Rhythms in the expression of pro-migratory factors and migration capacities were preserved in human primary leukocytes. The definition of spatial and temporal expression profiles of pro-migratory factors guiding leukocyte migration patterns to organs provides a resource for the further study of the impact of circadian rhythms in immunity.

Keywords: circadian; immunology; leukocyte; migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / immunology
  • Cell Adhesion Molecules / metabolism
  • Cell Movement / genetics
  • Cell Movement / immunology*
  • Circadian Rhythm / immunology*
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation / immunology*
  • Homeostasis / genetics
  • Homeostasis / immunology
  • Humans
  • Leukocytes / cytology
  • Leukocytes / immunology*
  • Leukocytes / metabolism
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Middle Aged
  • Organ Specificity / genetics
  • Organ Specificity / immunology
  • Transcription Factors / genetics
  • Transcription Factors / immunology*
  • Transcription Factors / metabolism

Substances

  • Cell Adhesion Molecules
  • Transcription Factors