Maternal exposure to E 551 during pregnancy leads to genome-wide DNA methylation changes and metabolic disorders in the livers of pregnant mice and their fetuses

被引:5
|
作者
Zhan, Yingqi [1 ]
Lou, He [1 ]
Shou, Rongshang [1 ]
Li, Anyao [1 ]
Shang, Jiaxin [1 ]
Jin, Yanyan [1 ]
Li, Lu [1 ,2 ]
Zhu, Lidan [1 ]
Lu, Xiaoyan [1 ,3 ,4 ]
Fan, Xiaohui [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Pharmaceut Informat Inst, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Innovat Ctr Yangtze River Delta, Natl Key Lab Chinese Med Modernizat, Jiaxing 314102, Peoples R China
[3] Westlake Lab Life Sci & Biomed, Hangzhou 310058, Peoples R China
[4] Zhejiang Univ, Jinhua Inst, Jinhua 321016, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
E; 551; Pregnancy; Epigenetics; DNA methylation; Hepatic metabolic disorders; SYNTHETIC AMORPHOUS SILICA; INSULIN-RESISTANCE; SILVER NANOPARTICLES; GESTATIONAL EXPOSURE; DIABETES-MELLITUS; TOXICITY; FOOD; BIODISTRIBUTION; COMPLICATIONS; NANOMATERIAL;
D O I
10.1016/j.jhazmat.2023.133233
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The widespread use of nanoparticles in the food industry has raised concerns regarding their potential adverse effects on human health, particularly in vulnerable populations, including pregnant mothers and fetuses. However, studies evaluating the reproductive and developmental toxicity of food-grade nanomaterials are limited. This study investigated the potential risks of prenatal dietary exposure to food-grade silica nanoparticles (E 551) on maternal health and fetal growth using conventional toxicological and epigenetic methods. The results showed that prenatal exposure to a high-dose of E 551 induces fetal resorption. Moreover, E 551 significantly accumulates in maternal and fetal livers, triggering a hepatic inflammatory response. At the epigenetic level, global DNA methylation is markedly altered in the maternal and fetal livers. Genome-wide DNA methylation sequencing revealed affected mCG, mCHG, and mCHH methylation landscapes. Subsequent bioinformatic analysis of the differentially methylated genes suggests that E 551 poses a risk of inducing metabolic disorders in maternal and fetal livers. This is further evidenced by impaired glucose tolerance in pregnant mice and altered expression of key metabolism-related genes and proteins in maternal and fetal livers. Collectively, the results of this study highlighted the importance of epigenetics in characterizing the potential toxicity of maternal exposure to food-grade nanomaterials during pregnancy.
引用
收藏
页数:19
相关论文
共 44 条
  • [1] Tobacco Smoking Leads to Extensive Genome-Wide Changes in DNA Methylation
    Zeilinger, Sonja
    Kuehnel, Brigitte
    Klopp, Norman
    Baurecht, Hansjoerg
    Kleinschmidt, Anja
    Gieger, Christian
    Weidinger, Stephan
    Lattka, Eva
    Adamski, Jerzy
    Peters, Annette
    Strauch, Konstantin
    Waldenberger, Melanie
    Illig, Thomas
    PLOS ONE, 2013, 8 (05):
  • [2] Genome-wide DNA methylation in neonates exposed to maternal depression, anxiety, or SSRI medication during pregnancy
    Non, Amy L.
    Binder, Alexandra M.
    Kubzansky, Laura D.
    Michels, Karin B.
    EPIGENETICS, 2014, 9 (07) : 964 - 972
  • [3] Evaluating genome-wide DNA methylation changes in mice by Methylation Specific Digital Karyotyping
    Boon, Kathy
    Tomfohr, John K.
    Bailey, Nathaniel W.
    Garantziotis, Stavros
    Li, Zhuowei
    Brass, David M.
    Maruoka, Shuichiro
    Hollingsworth, John W.
    Schwartz, David A.
    BMC GENOMICS, 2008, 9 (1)
  • [4] Evaluating genome-wide DNA methylation changes in mice by Methylation Specific Digital Karyotyping
    Kathy Boon
    John K Tomfohr
    Nathaniel W Bailey
    Stavros Garantziotis
    Zhuowei Li
    David M Brass
    Shuichiro Maruoka
    John W Hollingsworth
    David A Schwartz
    BMC Genomics, 9
  • [5] Absence of genome-wide changes in DNA methylation during development of the zebrafish
    Donald Macleod
    Victoria H. Clark
    Adrian Bird
    Nature Genetics, 1999, 23 : 139 - 140
  • [6] Genome-wide DNA methylation analysis of Hashimoto's thyroiditis during pregnancy
    Wenqian, Cai
    Fan, Wenlei
    Hu, Xijiang
    FEBS OPEN BIO, 2020, 10 (12): : 2780 - 2790
  • [7] DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis
    Joubert, Bonnie R.
    Felix, Janine F.
    Yousefi, Paul
    Bakulski, Kelly M.
    Just, Allan C.
    Breton, Carrie
    Reese, Sarah E.
    Markunas, Christina A.
    Richmond, Rebecca C.
    Xu, Cheng-Jian
    Kupers, Leanne K.
    Oh, Sam S.
    Hoyo, Cathrine
    Gruzieva, Olena
    Soderhal, Cilla
    Salas, Lucas A.
    Baiz, Nour
    Zhang, Hongmei
    Lepeule, Johanna
    Ruiz, Carlos
    Ligthart, Symen
    Wang, Tianyuan
    Taylor, Jack A.
    Duijts, Liesbeth
    Sharp, Gemma C.
    Jankipersadsing, Soesma A.
    Nilsen, Roy M.
    Vaez, Ahmad
    Fallin, M. Daniele
    Hu, Donglei
    Litonjua, Augusto A.
    Fuemmeler, Bernard F.
    Huen, Karen
    Kere, Juha
    Kull, Inger
    Munthe-Kaas, Monica Cheng
    Gehring, Ulrike
    Bustamante, Mariona
    Saurel-Coubizolles, Marie Jose
    Quraishi, Bilal M.
    Ren, Jie
    Tost, Jorg
    Gonzalez, Juan R.
    Peters, Marjolein J.
    Haberg, Siri E.
    Xu, Zongli
    van Meurs, Joyce B.
    Gaunt, Tom R.
    Kerkhof, Marjan
    Corpeleijn, Eva
    AMERICAN JOURNAL OF HUMAN GENETICS, 2016, 98 (04) : 680 - 696
  • [8] Dynamic Changes of Genome-Wide DNA Methylation during Soybean Seed Development
    Yong-qiang Charles An
    Wolfgang Goettel
    Qiang Han
    Arthur Bartels
    Zongrang Liu
    Wenyan Xiao
    Scientific Reports, 7
  • [9] Dynamic Changes of Genome-Wide DNA Methylation during Soybean Seed Development
    An, Yong-qiang Charles
    Goettel, Wolfgang
    Han, Qiang
    Bartels, Arthur
    Liu, Zongrang
    Xiao, Wenyan
    SCIENTIFIC REPORTS, 2017, 7
  • [10] Sequential changes in genome-wide DNA methylation status during adipocyte differentiation
    Sakamoto, Hideki
    Kogo, Yasushi
    Ohgane, Jun
    Hattori, Naka
    Yagi, Shintaro
    Tanaka, Satoshi
    Shiota, Kunio
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 366 (02) : 360 - 366