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Progenitor cells are mobilized by acute psychological stress but not beta-adrenergic receptor agonist infusion

  • Natalie E. Riddell*
  • , Victoria E. Burns
  • , Graham R. Wallace
  • , Kate M. Edwards
  • , Mark Drayson
  • , Laura S. Redwine
  • , Suzi Hong
  • , Jack C. Bui
  • , Johannes C. Fischer
  • , Paul J. Mills
  • , Jos A. Bosch
  • *Corresponding author for this work
  • University College London
  • University of Birmingham
  • The University of Sydney
  • University of California at San Diego
  • Heinrich Heine University Düsseldorf

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objectives: Stimuli that activate the sympathetic nervous system, such as acute psychological stress, rapidly invoke a robust mobilization of lymphocytes into the circulation. Experimental animal studies suggest that bone marrow-derived progenitor cells (PCs) also mobilize in response to sympathetic stimulation. Here we tested the effects of acute psychological stress and brief pharmacological β-adrenergic (βAR) stimulation on peripheral PC numbers in humans. Methods: In two studies, we investigated PC mobilization in response to an acute speech task (n=26) and βAR-agonist (isoproterenol) infusion (n=20). A subset of 8 participants also underwent the infusion protocol with concomitant administration of the βAR-antagonist propranolol. Flow cytometry was used to enumerate lymphocyte subsets, total progenitor cells, total haematopoietic stem cells (HSC), early HSC (multi-lineage potential), late HSC (lineage committed), and endothelial PCs (EPCs). Results: Both psychological stress and βAR-agonist infusion caused the expected mobilization of total monocytes and lymphocytes and CD8+ T lymphocytes. Psychological stress also induced a modest, but significant, increase in total PCs, HSCs, and EPC numbers in peripheral blood. However, infusion of a βAR-agonist did not result in a significant change in circulating PCs. Conclusion: PCs are rapidly mobilized by psychological stress via mechanisms independent of βAR-stimulation, although the findings do not exclude βAR-stimulation as a possible cofactor. Considering the clinical and physiological relevance, further research into the mechanisms involved in stress-induced PC mobilization seems warranted.

Original languageEnglish
Pages (from-to)49-53
Number of pages5
JournalBrain, behavior, and immunity
Volume49
DOIs
Publication statusPublished - 1 Oct 2015

Keywords

  • Adrenergic
  • Mobilization
  • Progenitor cells
  • Psychological stress
  • βAR-stimulation

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