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Cell-free DNA release under psychosocial and physical stress conditions
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 stre...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206142/ https://www.ncbi.nlm.nih.gov/pubmed/30374018 http://dx.doi.org/10.1038/s41398-018-0264-x |
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author | 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. |
author_facet | 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. |
author_sort | Hummel, E. M. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6206142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62061422018-11-02 Cell-free DNA release under psychosocial and physical stress conditions 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. Transl Psychiatry Article 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. Nature Publishing Group UK 2018-10-29 /pmc/articles/PMC6206142/ /pubmed/30374018 http://dx.doi.org/10.1038/s41398-018-0264-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article 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. Cell-free DNA release under psychosocial and physical stress conditions |
title | Cell-free DNA release under psychosocial and physical stress conditions |
title_full | Cell-free DNA release under psychosocial and physical stress conditions |
title_fullStr | Cell-free DNA release under psychosocial and physical stress conditions |
title_full_unstemmed | Cell-free DNA release under psychosocial and physical stress conditions |
title_short | Cell-free DNA release under psychosocial and physical stress conditions |
title_sort | cell-free dna release under psychosocial and physical stress conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206142/ https://www.ncbi.nlm.nih.gov/pubmed/30374018 http://dx.doi.org/10.1038/s41398-018-0264-x |
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