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Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients
BACKGROUND: Multiple sclerosis (MS) is thought to be a T cell-mediated autoimmune disorder. MS pathogenesis is likely due to a genetic predisposition triggered by a variety of environmental factors. Epigenetics, particularly DNA methylation, provide a logical interface for environmental factors to i...
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/PMC4635618/ https://www.ncbi.nlm.nih.gov/pubmed/26550040 http://dx.doi.org/10.1186/s13148-015-0152-7 |
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author | Maltby, Vicki E. Graves, Moira C. Lea, Rodney A. Benton, Miles C. Sanders, Katherine A. Tajouri, Lotti Scott, Rodney J. Lechner-Scott, Jeannette |
author_facet | Maltby, Vicki E. Graves, Moira C. Lea, Rodney A. Benton, Miles C. Sanders, Katherine A. Tajouri, Lotti Scott, Rodney J. Lechner-Scott, Jeannette |
author_sort | Maltby, Vicki E. |
collection | PubMed |
description | BACKGROUND: Multiple sclerosis (MS) is thought to be a T cell-mediated autoimmune disorder. MS pathogenesis is likely due to a genetic predisposition triggered by a variety of environmental factors. Epigenetics, particularly DNA methylation, provide a logical interface for environmental factors to influence the genome. In this study we aim to identify DNA methylation changes associated with MS in CD8+ T cells in 30 relapsing remitting MS patients and 28 healthy blood donors using Illumina 450K methylation arrays. FINDINGS: Seventy-nine differentially methylated CpGs were associated with MS. The methylation profile of CD8+ T cells was distinctive from our previously published data on CD4+ T cells in the same cohort. Most notably, there was no major CpG effect at the MS risk gene HLA-DRB1 locus in the CD8+ T cells. CONCLUSION: CD8+ T cells and CD4+ T cells have distinct DNA methylation profiles. This case–control study highlights the importance of distinctive cell subtypes when investigating epigenetic changes in MS and other complex diseases. |
format | Online Article Text |
id | pubmed-4635618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46356182015-11-07 Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients Maltby, Vicki E. Graves, Moira C. Lea, Rodney A. Benton, Miles C. Sanders, Katherine A. Tajouri, Lotti Scott, Rodney J. Lechner-Scott, Jeannette Clin Epigenetics Short Report BACKGROUND: Multiple sclerosis (MS) is thought to be a T cell-mediated autoimmune disorder. MS pathogenesis is likely due to a genetic predisposition triggered by a variety of environmental factors. Epigenetics, particularly DNA methylation, provide a logical interface for environmental factors to influence the genome. In this study we aim to identify DNA methylation changes associated with MS in CD8+ T cells in 30 relapsing remitting MS patients and 28 healthy blood donors using Illumina 450K methylation arrays. FINDINGS: Seventy-nine differentially methylated CpGs were associated with MS. The methylation profile of CD8+ T cells was distinctive from our previously published data on CD4+ T cells in the same cohort. Most notably, there was no major CpG effect at the MS risk gene HLA-DRB1 locus in the CD8+ T cells. CONCLUSION: CD8+ T cells and CD4+ T cells have distinct DNA methylation profiles. This case–control study highlights the importance of distinctive cell subtypes when investigating epigenetic changes in MS and other complex diseases. BioMed Central 2015-11-05 /pmc/articles/PMC4635618/ /pubmed/26550040 http://dx.doi.org/10.1186/s13148-015-0152-7 Text en © Maltby et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 | Short Report Maltby, Vicki E. Graves, Moira C. Lea, Rodney A. Benton, Miles C. Sanders, Katherine A. Tajouri, Lotti Scott, Rodney J. Lechner-Scott, Jeannette Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title | Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title_full | Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title_fullStr | Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title_full_unstemmed | Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title_short | Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients |
title_sort | genome-wide dna methylation profiling of cd8+ t cells shows a distinct epigenetic signature to cd4+ t cells in multiple sclerosis patients |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635618/ https://www.ncbi.nlm.nih.gov/pubmed/26550040 http://dx.doi.org/10.1186/s13148-015-0152-7 |
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