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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...

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Autores principales: Tserel, Liina, Limbach, Maia, Saare, Mario, Kisand, Kai, Metspalu, Andres, Milani, Lili, Peterson, Pärt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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