Journal of Applied Physiology
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J Appl Physiol 102: 26-36, 2007. First published September 21, 2006; doi:10.1152/japplphysiol.00066.2006
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Exercise affects the gene expression profiles of human white blood cells

Petra Büttner,1 Sandy Mosig,1 Anja Lechtermann,2 Harald Funke,1 and Frank C. Mooren3

1Institute of Vascular Biology and Medicine, Friedrich-Schiller-University Jena, Jena; 2Institute of Sports Medicine, University Hospital Münster, Münster; and 3Department of Sports Medicine, Institute of Sports Sciences, Justus-Liebig-University, Giessen, Germany

Submitted 19 January 2006 ; accepted in final form 5 September 2006

White blood cells (WBCs) express tens of thousands of genes, whose expression levels are modified by genetic and external factors. The purpose of the present study was to investigate the effects of acute exercise on gene expression profiles (GEPs) of WBCs and to identify suitable genes that may serve as surrogate markers for monitoring exercise and training load. Five male participants performed an exhaustive treadmill test (ET) at 80% of their maximal O2 uptake (VO2 max) and a moderate treadmill test (MT) at 60% VO2 max for exactly the same time ~2 wk later. WBCs were isolated by the erythrocyte lysis method. GEPs were measured using the Affymetrix GeneChip technology. After scaling, normalization, and filtering, groupwise comparisons of gene expression intensities were performed, and several measurements were validated by real-time PCR. We found 450 genes upregulated and 150 downregulated (>1.5-fold change; ANOVA with Benjamini-Hochberg correction, P < 0.05) after ET that were closely associated with the gene ontology lists "response to stress" and "inflammatory response". Analysis of mean expression levels after MT showed that the extent of up- and downregulation was workload dependent. The genes for the stress (heat shock) proteins HSPA1A and HSPH1 and for the matrix metalloproteinase MMP-9 showed the most prominent increases, whereas the YES1 oncogene (YES1) and CD160 (BY55) were most strongly reduced. Despite different methodological approaches used, the consistency of our results with the expression data of another study (Connolly PH, Caiozzo VJ, Zaldivar F, Nemet D, Larson J, Hung SP, Heck JD, Hatfield GW, Cooper DM. J Appl Physiol 97: 1461–1469, 2004) suggests that expression fingerprints are useful tools for monitoring exercise and training loads and thereby help to avoid training-associated health risks.

inflammation; stress response; microarrays; surrogate marker



Address for reprint requests and other correspondence: F. C. Mooren, Dept. of Sports Medicine, Institute of Sports Sciences, Justus-Liebig-Univ., Kugelberg 62, 35394 Giessen, Germany (e-mail: frank-christoph.mooren{at}sport.uni-giessen.de)




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