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A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood
BACKGROUND: Many recent epigenetic studies report that cigarette smoking reduces DNA methylation in whole blood at the single CpG site cg19859270 within the GPR15 gene. RESULTS: Within two independent cohorts, we confirmed the differentially expression of the GPR15 gene when smokers and non-smokers...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526203/ https://www.ncbi.nlm.nih.gov/pubmed/26246861 http://dx.doi.org/10.1186/s13148-015-0113-1 |
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author | Bauer, Mario Linsel, Gunter Fink, Beate Offenberg, Kirsten Hahn, Anne Maria Sack, Ulrich Knaack, Heike Eszlinger, Markus Herberth, Gunda |
author_facet | Bauer, Mario Linsel, Gunter Fink, Beate Offenberg, Kirsten Hahn, Anne Maria Sack, Ulrich Knaack, Heike Eszlinger, Markus Herberth, Gunda |
author_sort | Bauer, Mario |
collection | PubMed |
description | BACKGROUND: Many recent epigenetic studies report that cigarette smoking reduces DNA methylation in whole blood at the single CpG site cg19859270 within the GPR15 gene. RESULTS: Within two independent cohorts, we confirmed the differentially expression of the GPR15 gene when smokers and non-smokers subjects are compared. By validating the GPR15 protein expression at the cellular level, we found that the observed decreased methylation at this site in white blood cells (WBC) of smokers is mainly caused by the high proportion of CD3+GPR15+ expressing T cells in peripheral blood. In current smokers, the percentage of GPR15+ cells among CD3+ T cells in peripheral blood is significantly higher (15.5 ± 7.2 %, mean ± standard deviation) compared to non-smokers (3.7 ± 1.6 %). Treatment of peripheral blood mononuclear cell (PBMC) cultures with aqueous cigarette smoke extract did not induce a higher proportion of this T cell subtype. CONCLUSIONS: Our results underline that DNA hypomethylation at cg19859270 site, observed in WBCs of smokers, did not arise by direct effect of tobacco smoking compounds on methylation of DNA but rather by the enrichment of a tobacco-smoking-induced lymphocyte population in the peripheral blood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0113-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4526203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45262032015-08-06 A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood Bauer, Mario Linsel, Gunter Fink, Beate Offenberg, Kirsten Hahn, Anne Maria Sack, Ulrich Knaack, Heike Eszlinger, Markus Herberth, Gunda Clin Epigenetics Research BACKGROUND: Many recent epigenetic studies report that cigarette smoking reduces DNA methylation in whole blood at the single CpG site cg19859270 within the GPR15 gene. RESULTS: Within two independent cohorts, we confirmed the differentially expression of the GPR15 gene when smokers and non-smokers subjects are compared. By validating the GPR15 protein expression at the cellular level, we found that the observed decreased methylation at this site in white blood cells (WBC) of smokers is mainly caused by the high proportion of CD3+GPR15+ expressing T cells in peripheral blood. In current smokers, the percentage of GPR15+ cells among CD3+ T cells in peripheral blood is significantly higher (15.5 ± 7.2 %, mean ± standard deviation) compared to non-smokers (3.7 ± 1.6 %). Treatment of peripheral blood mononuclear cell (PBMC) cultures with aqueous cigarette smoke extract did not induce a higher proportion of this T cell subtype. CONCLUSIONS: Our results underline that DNA hypomethylation at cg19859270 site, observed in WBCs of smokers, did not arise by direct effect of tobacco smoking compounds on methylation of DNA but rather by the enrichment of a tobacco-smoking-induced lymphocyte population in the peripheral blood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0113-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-06 /pmc/articles/PMC4526203/ /pubmed/26246861 http://dx.doi.org/10.1186/s13148-015-0113-1 Text en © Bauer et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Bauer, Mario Linsel, Gunter Fink, Beate Offenberg, Kirsten Hahn, Anne Maria Sack, Ulrich Knaack, Heike Eszlinger, Markus Herberth, Gunda A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title | A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title_full | A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title_fullStr | A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title_full_unstemmed | A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title_short | A varying T cell subtype explains apparent tobacco smoking induced single CpG hypomethylation in whole blood |
title_sort | varying t cell subtype explains apparent tobacco smoking induced single cpg hypomethylation in whole blood |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526203/ https://www.ncbi.nlm.nih.gov/pubmed/26246861 http://dx.doi.org/10.1186/s13148-015-0113-1 |
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