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Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells
Recent studies have identified carbon nanotube (CNT)-induced epigenetic changes as one of the key players in patho-physiological response. In the present study, we investigated whether CNT exposure is associated with epigenetic changes in human bronchial epithelial cells (16 HBE), in vitro. We focus...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945544/ https://www.ncbi.nlm.nih.gov/pubmed/29755656 http://dx.doi.org/10.18632/oncotarget.24866 |
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author | Ghosh, Manosij Öner, Deniz Duca, Radu C. Bekaert, Bram Vanoirbeek, Jeroen A.J. Godderis, Lode Hoet, Peter H.M. |
author_facet | Ghosh, Manosij Öner, Deniz Duca, Radu C. Bekaert, Bram Vanoirbeek, Jeroen A.J. Godderis, Lode Hoet, Peter H.M. |
author_sort | Ghosh, Manosij |
collection | PubMed |
description | Recent studies have identified carbon nanotube (CNT)-induced epigenetic changes as one of the key players in patho-physiological response. In the present study, we investigated whether CNT exposure is associated with epigenetic changes in human bronchial epithelial cells (16 HBE), in vitro. We focused on global DNA methylation, methylation of LINE-1 elements and promoter sequence of twelve functionally important genes (SKI, DNMT1, HDAC4, NPAT, ATM, BCL2L11, MAP3K10, PIK3R2, MYO1C, TCF3, FGFR 1 and AGRN). Additionally, we studied the influence of CNT exposure on miRNA expression. Using a LC-MS/MS method and pyrosequencing for LINE-1, we observed no significant changes in global DNA methylation (%) between the concentrations of multi-walled and single-walled CNT (MWCNT and SWCNT, respectively). Significant changes in sequence-specific methylation was observed in at least one CpG site for DNMT1 (SWCNT), HDAC4 (MWCNT), NPAT/ATM (MWCNT and SWCNT), MAP3K10 (MWCNT), PIK3R2 (MWCNT and SWCNT) and MYO1C (SWCNT). While changes in DNA methylation of the genes were relatively small, these changes were associated with changes in RNA expression, especially for MWCNT. However, the study did not reveal any significant alteration in the miRNA expression, associated with MWCNT and SWCNT exposure. Based on our results, mainly MWCNT influence DNA methylation and expression of the studied genes and could have significant impact on several critical cellular processes. |
format | Online Article Text |
id | pubmed-5945544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59455442018-05-13 Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells Ghosh, Manosij Öner, Deniz Duca, Radu C. Bekaert, Bram Vanoirbeek, Jeroen A.J. Godderis, Lode Hoet, Peter H.M. Oncotarget Research Paper Recent studies have identified carbon nanotube (CNT)-induced epigenetic changes as one of the key players in patho-physiological response. In the present study, we investigated whether CNT exposure is associated with epigenetic changes in human bronchial epithelial cells (16 HBE), in vitro. We focused on global DNA methylation, methylation of LINE-1 elements and promoter sequence of twelve functionally important genes (SKI, DNMT1, HDAC4, NPAT, ATM, BCL2L11, MAP3K10, PIK3R2, MYO1C, TCF3, FGFR 1 and AGRN). Additionally, we studied the influence of CNT exposure on miRNA expression. Using a LC-MS/MS method and pyrosequencing for LINE-1, we observed no significant changes in global DNA methylation (%) between the concentrations of multi-walled and single-walled CNT (MWCNT and SWCNT, respectively). Significant changes in sequence-specific methylation was observed in at least one CpG site for DNMT1 (SWCNT), HDAC4 (MWCNT), NPAT/ATM (MWCNT and SWCNT), MAP3K10 (MWCNT), PIK3R2 (MWCNT and SWCNT) and MYO1C (SWCNT). While changes in DNA methylation of the genes were relatively small, these changes were associated with changes in RNA expression, especially for MWCNT. However, the study did not reveal any significant alteration in the miRNA expression, associated with MWCNT and SWCNT exposure. Based on our results, mainly MWCNT influence DNA methylation and expression of the studied genes and could have significant impact on several critical cellular processes. Impact Journals LLC 2018-04-17 /pmc/articles/PMC5945544/ /pubmed/29755656 http://dx.doi.org/10.18632/oncotarget.24866 Text en Copyright: © 2018 Ghosh et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ghosh, Manosij Öner, Deniz Duca, Radu C. Bekaert, Bram Vanoirbeek, Jeroen A.J. Godderis, Lode Hoet, Peter H.M. Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title | Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title_full | Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title_fullStr | Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title_full_unstemmed | Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title_short | Single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 HBE cells |
title_sort | single-walled and multi-walled carbon nanotubes induce sequence-specific epigenetic alterations in 16 hbe cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945544/ https://www.ncbi.nlm.nih.gov/pubmed/29755656 http://dx.doi.org/10.18632/oncotarget.24866 |
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