Cell-free DNA release under psychosocial and physical stress conditions

• Published in: Translational psychiatry Vol. 8; no. 1; pp. 236 - 10
• Main Authors: Hummel, E. M., Hessas, E., Müller, S., Beiter, T., Fisch, M., Eibl, A., Wolf, O. T., Giebel, B., Platen, P., Kumsta, R., Moser, D. A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29.10.2018; Nature Publishing Group
• Subjects: 45; 45/22; 45/23; 45/77; 631/477; 692/53; Behavioral Sciences; Biological Psychology; Deoxyribonucleic acid; DNA; DNA methylation; Exercise; Medicine; Medicine & Public Health; Mitochondrial DNA; Neurosciences; Pharmacotherapy; Psychiatry
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/s41398-018-0264-x

The understanding of mechanisms linking psychological stress to disease risk depend on reliable stress biomarkers. Circulating cell-free DNA (cfDNA) has emerged as a potential biomarker of cellular stress, aging, inflammatory processes, and cell death. Recent studies indicated that psychosocial stress and physical exercise might also influence its release. We compared the effects of acute psychosocial and physical exercise stress on cfDNA release by exposing 20 young, healthy men to both an acute psychosocial laboratory stressor and an acute physical exercise stressor. Venous blood and saliva samples were collected before and after stress exposure. Cell-free DNA was extracted from plasma and quantified by qPCR. Furthermore, cfDNA fragment length was analyzed and cfDNA methylation patterns were assayed across time. In addition, release of stress hormones and subjective stress responses were measured. Results showed a twofold increase of cfDNA after TSST and fivefold increase after exhaustive treadmill exercise, with an overabundance of shorter cfDNA fragments after physical exhaustion. Interestingly, cell-free mitochondrial DNA showed similar increase after both stress paradigms. Furthermore, cfDNA methylation signatures—used here as a marker for diverse cellular origin—were significantly different post stress tests. While DNA methylation decreased immediately after psychosocial stress, it increased after physical stress, suggesting different cellular sources of active DNA release. In summary, our results suggest stimulus and cell-specific regulation of cfDNA release. Whereas the functional role of stress-associated cfDNA release remains elusive, it might serve as a valuable biomarker in molecular stress research as a part of the psychophysiological stress response.