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10.1016/j.stemcr.2017.07.010

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suck abstract from ncbi


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pmid28803917
      Stem+Cell+Reports 2017 ; 9 (3 ): 762-769
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  • SCA1(+) Cells from the Heart Possess a Molecular Circadian Clock and Display Circadian Oscillations in Cellular Functions #MMPMID28803917
  • Du Pré BC ; Demkes EJ ; Feyen DAM ; Dierickx P ; Crnko S ; Kok BJM ; Sluijter JPG ; Doevendans PA ; Vos MA ; Van Veen TAB ; Van Laake LW
  • Stem Cell Reports 2017[Sep]; 9 (3 ): 762-769 PMID28803917 show ga
  • Stem cell antigen 1-positive (SCA1(+)) cells (SPCs) have been investigated in cell-based cardiac repair and pharmacological research, although improved cardiac function after injection has been variable and the mode of action remains unclear. Circadian (24-hr) rhythms are biorhythms regulated by molecular clocks that play an important role in (patho)physiology. Here, we describe (1) the presence of a molecular circadian clock in SPCs and (2) circadian rhythmicity in SPC function. We isolated SPCs from human fetal heart and found that these cells possess a molecular clock based on typical oscillations in core clock components BMAL1 and CRY1. Functional analyses revealed that circadian rhythmicity also governs SPC proliferation, stress tolerance, and growth factor release, with large differences between peaks and troughs. We conclude that SPCs contain a circadian molecular clock that controls crucial cellular functions. Taking circadian rhythms into account may improve reproducibility and outcome of research and therapies using SPCs.
  • |*Circadian Clocks [MESH]
  • |*Circadian Rhythm [MESH]
  • |ARNTL Transcription Factors/metabolism [MESH]
  • |Apoptosis [MESH]
  • |Ataxin-1/*metabolism [MESH]
  • |Cell Movement [MESH]
  • |Cell Proliferation [MESH]
  • |Cell Separation [MESH]
  • |Humans [MESH]
  • |Intercellular Signaling Peptides and Proteins/metabolism [MESH]
  • |Myocardium/*cytology/*metabolism [MESH]
  • |Paracrine Communication [MESH]


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