Fish oil supplementation induces Expression of genes related to cell cycle, endoplasmic reticulum stress and apoptosis in peripheral blood mononuclear cells: a transcriptomic approach
Myhrstad, Mari; Ulven, Stine Marie; Günther, Clara-Cecilie; Ottestad, Inger; Holden, Marit; Ryeng, Einar; Borge, Grethe Iren Andersen; Kohler, Achim; Brønner, Kirsti Wettre; Thoresen, Magne; Holven, Kirsten Bjørklund
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© 2014 the authors. journal of internal medicine published by john wiley & sons ltd on behalf of the association for the publication of the journal of internal medicine. this is an open access article under the terms of the creative commons attribution license, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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2014Metadata
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Myhrstad, M. C., Ulven, S. M., Günther, C. C., Ottestad, I., Holden, M., Ryeng, E., ... & Holven, K. B. (2014). Fish oil supplementation induces expression of genes related to cell cycle, endoplasmic reticulum stress and apoptosis in peripheral blood mononuclear cells: a transcriptomic approach. Journal of internal medicine, 276(5), 498-511. http://dx.doi.org/10.1111/joim.12217Abstract
Background. Fish oil supplementation has been shown
to alter gene expression of mononuclear cells both in
vitro and in vivo. However, little is known about the
total transcriptome profile in healthy subjects after
intake of fish oil. We therefore investigated the gene
expression profile in peripheral blood mononuclear
cells (PBMCs) after intake of fish oil for 7 weeks
using transcriptome analyses.
Design. In a 7-week, double-blinded, randomized, controlled,
parallel-group study, healthy subjects
received 8 g day 1 fish oil (1.6 g day 1 eicosapentaenoic
acid + docosahexaenoic acid) (n = 17) or
8 g day 1 high oleic sunflower oil (n = 19). Microarray
analyses of RNA isolated from PBMCs were performed
at baseline and after 7 weeks of intervention. Results. Cell cycle, DNA packaging and chromosome
organization are biological processes found to be
upregulated after intake of fish oil compared to
high oleic sunflower oil using a moderated t-test.
In addition, gene set enrichment analysis identified
several enriched gene sets after intake of fish
oil. The genes contributing to the significantly
different gene sets in the subjects given fish oil
compared with the control group are involved in
cell cycle, endoplasmic reticulum (ER) stress and
apoptosis. Gene transcripts with common motifs
for 35 known transcription factors including E2F,
TP53 and ATF4 were upregulated after intake of
fish oil.
Conclusion. We have shown that intake of fish oil for
7 weeks modulates gene expression in PBMCs of
healthy subjects. The increased expression of
genes related to cell cycle, ER stress and apoptosis
suggests that intake of fish oil may modulate basic
cellular processes involved in normal cellular function.