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CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing
BACKGROUND: Ageing affects many components of the immune system, including innate immune cells like monocytes. They are important in the early response to pathogens and for their role to differentiate into macrophages and dendritic cells. Recent studies have revealed significant age-related changes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896835/ https://www.ncbi.nlm.nih.gov/pubmed/24405718 http://dx.doi.org/10.1186/1742-4933-11-1 |
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author | Tserel, Liina Limbach, Maia Saare, Mario Kisand, Kai Metspalu, Andres Milani, Lili Peterson, Pärt |
author_facet | Tserel, Liina Limbach, Maia Saare, Mario Kisand, Kai Metspalu, Andres Milani, Lili Peterson, Pärt |
author_sort | Tserel, Liina |
collection | PubMed |
description | BACKGROUND: Ageing affects many components of the immune system, including innate immune cells like monocytes. They are important in the early response to pathogens and for their role to differentiate into macrophages and dendritic cells. Recent studies have revealed significant age-related changes in genomic DNA methylation in peripheral blood mononuclear cells, however information on epigenetic changes in specific leukocyte subsets is still lacking. Here, we aimed to analyse DNA methylation in purified monocyte populations from young and elderly individuals. FINDINGS: We analysed the methylation changes in monocytes purified from young and elderly individuals using the HumanMethylation450 BeadChip array. Interestingly, we found that among 26 differentially methylated CpG sites, the majority of sites were hypomethylated in elderly individuals. The most hypomethylated CpG sites were located in neuropilin 1 (NRP1; cg24892069) and neurexin 2 (NRXN2; cg27209729) genes, and upstream of miR-29b-2 gene (cg10501210). The age-related hypomethylation of these three sites was confirmed in a separate group of young and elderly individuals. CONCLUSIONS: We identified significant age-related hypomethylation in human purified monocytes at CpG sites within the regions of NRP1, NRXN2 and miR-29b-2 genes. |
format | Online Article Text |
id | pubmed-3896835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38968352014-01-22 CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing Tserel, Liina Limbach, Maia Saare, Mario Kisand, Kai Metspalu, Andres Milani, Lili Peterson, Pärt Immun Ageing Short Report BACKGROUND: Ageing affects many components of the immune system, including innate immune cells like monocytes. They are important in the early response to pathogens and for their role to differentiate into macrophages and dendritic cells. Recent studies have revealed significant age-related changes in genomic DNA methylation in peripheral blood mononuclear cells, however information on epigenetic changes in specific leukocyte subsets is still lacking. Here, we aimed to analyse DNA methylation in purified monocyte populations from young and elderly individuals. FINDINGS: We analysed the methylation changes in monocytes purified from young and elderly individuals using the HumanMethylation450 BeadChip array. Interestingly, we found that among 26 differentially methylated CpG sites, the majority of sites were hypomethylated in elderly individuals. The most hypomethylated CpG sites were located in neuropilin 1 (NRP1; cg24892069) and neurexin 2 (NRXN2; cg27209729) genes, and upstream of miR-29b-2 gene (cg10501210). The age-related hypomethylation of these three sites was confirmed in a separate group of young and elderly individuals. CONCLUSIONS: We identified significant age-related hypomethylation in human purified monocytes at CpG sites within the regions of NRP1, NRXN2 and miR-29b-2 genes. BioMed Central 2014-01-09 /pmc/articles/PMC3896835/ /pubmed/24405718 http://dx.doi.org/10.1186/1742-4933-11-1 Text en Copyright © 2014 Tserel et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Tserel, Liina Limbach, Maia Saare, Mario Kisand, Kai Metspalu, Andres Milani, Lili Peterson, Pärt CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title | CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title_full | CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title_fullStr | CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title_full_unstemmed | CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title_short | CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing |
title_sort | cpg sites associated with nrp1, nrxn2 and mir-29b-2 are hypomethylated in monocytes during ageing |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896835/ https://www.ncbi.nlm.nih.gov/pubmed/24405718 http://dx.doi.org/10.1186/1742-4933-11-1 |
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