DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.

The toxic effects of silica nanoparticles (SiNPs) are raising concerns due to its widely applications in biomedicine. However, current information about the epigenetic toxicity of SiNPs is insufficient. In this study, the epigenetic regulation of low-dose exposure to SiNPs was evaluated in human bro...

Full description

Bibliographic Details
Main Authors: Yang Zou, Qiuling Li, Lizhen Jiang, Caixia Guo, Yanbo Li, Yang Yu, Yang Li, Junchao Duan, Zhiwei Sun
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4928798?pdf=render
_version_ 1818986188192612352
author Yang Zou
Qiuling Li
Lizhen Jiang
Caixia Guo
Yanbo Li
Yang Yu
Yang Li
Junchao Duan
Zhiwei Sun
author_facet Yang Zou
Qiuling Li
Lizhen Jiang
Caixia Guo
Yanbo Li
Yang Yu
Yang Li
Junchao Duan
Zhiwei Sun
author_sort Yang Zou
collection DOAJ
description The toxic effects of silica nanoparticles (SiNPs) are raising concerns due to its widely applications in biomedicine. However, current information about the epigenetic toxicity of SiNPs is insufficient. In this study, the epigenetic regulation of low-dose exposure to SiNPs was evaluated in human bronchial epithelial BEAS-2B cells over 30 passages. Cell viability was decreased in a dose- and passage-dependent manner. The apoptotic rate, the expression of caspase-9 and caspase-3, were significantly increased induced by SiNPs. HumanMethylation450 BeadChip analysis identified that the PI3K/Akt as the primary apoptosis-related pathway among the 25 significant altered processes. The differentially methylated sites of PI3K/Akt pathway involved 32 differential genes promoters, in which the CREB3L1 and Bcl-2 were significant hypermethylated. The methyltransferase inhibitor, 5-aza, further verified that the DNA hypermethylation status of CREB3L1 and Bcl-2 were associated with downregulation of their mRNA levels. In addition, mitochondrial-mediated apoptosis was triggered by SiNPs via the downregulation of PI3K/Akt/CREB/Bcl-2 signaling pathway. Our findings suggest that long-term low-dose exposure to SiNPs could lead to epigenetic alterations.
first_indexed 2024-12-20T18:46:49Z
format Article
id doaj.art-b5c665b78bea43db8dc5871f75b03ebb
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-20T18:46:49Z
publishDate 2016-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-b5c665b78bea43db8dc5871f75b03ebb2022-12-21T19:29:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01116e015847510.1371/journal.pone.0158475DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.Yang ZouQiuling LiLizhen JiangCaixia GuoYanbo LiYang YuYang LiJunchao DuanZhiwei SunThe toxic effects of silica nanoparticles (SiNPs) are raising concerns due to its widely applications in biomedicine. However, current information about the epigenetic toxicity of SiNPs is insufficient. In this study, the epigenetic regulation of low-dose exposure to SiNPs was evaluated in human bronchial epithelial BEAS-2B cells over 30 passages. Cell viability was decreased in a dose- and passage-dependent manner. The apoptotic rate, the expression of caspase-9 and caspase-3, were significantly increased induced by SiNPs. HumanMethylation450 BeadChip analysis identified that the PI3K/Akt as the primary apoptosis-related pathway among the 25 significant altered processes. The differentially methylated sites of PI3K/Akt pathway involved 32 differential genes promoters, in which the CREB3L1 and Bcl-2 were significant hypermethylated. The methyltransferase inhibitor, 5-aza, further verified that the DNA hypermethylation status of CREB3L1 and Bcl-2 were associated with downregulation of their mRNA levels. In addition, mitochondrial-mediated apoptosis was triggered by SiNPs via the downregulation of PI3K/Akt/CREB/Bcl-2 signaling pathway. Our findings suggest that long-term low-dose exposure to SiNPs could lead to epigenetic alterations.http://europepmc.org/articles/PMC4928798?pdf=render
spellingShingle Yang Zou
Qiuling Li
Lizhen Jiang
Caixia Guo
Yanbo Li
Yang Yu
Yang Li
Junchao Duan
Zhiwei Sun
DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
PLoS ONE
title DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
title_full DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
title_fullStr DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
title_full_unstemmed DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
title_short DNA Hypermethylation of CREB3L1 and Bcl-2 Associated with the Mitochondrial-Mediated Apoptosis via PI3K/Akt Pathway in Human BEAS-2B Cells Exposure to Silica Nanoparticles.
title_sort dna hypermethylation of creb3l1 and bcl 2 associated with the mitochondrial mediated apoptosis via pi3k akt pathway in human beas 2b cells exposure to silica nanoparticles
url http://europepmc.org/articles/PMC4928798?pdf=render
work_keys_str_mv AT yangzou dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT qiulingli dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT lizhenjiang dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT caixiaguo dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT yanboli dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT yangyu dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT yangli dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT junchaoduan dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles
AT zhiweisun dnahypermethylationofcreb3l1andbcl2associatedwiththemitochondrialmediatedapoptosisviapi3kaktpathwayinhumanbeas2bcellsexposuretosilicananoparticles