Parental exposure to bisphenol A affects pharyngeal cartilage development and causes global transcriptomic changes in zebrafish (Danio rerio) offspring

被引:31
作者
Huang, Wenlong [1 ]
Zheng, Shukai [1 ]
Xiao, Jiefeng [1 ]
Liu, Caixia [1 ]
Du, Taifeng [1 ]
Wu, Kusheng [1 ]
机构
[1] Shantou Univ, Dept Prevent Med, Med Coll, 22 Xinling Rd, Shantou 515041, Guangdong, Peoples R China
关键词
Bisphenol A (BPA); Zebrafish; Pharyngeal cartilage development; Embryotoxicity; Developmental toxicity; DIMERIZATION PROTEIN-2 JDP2; OXIDATIVE STRESS; ENDOCRINE DISRUPTION; SIGNALING PATHWAYS; IN-VITRO; TOXICITY; EMBRYOS; LARVAE; DIFFERENTIATION; OSTEOCLAST;
D O I
10.1016/j.chemosphere.2020.126537
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: As one of the most common endocrine-disrupting chemicals (EDCs), bisphenol A (BPA) is a threat to aquatic ecosystems. Despite a rich literature addressing the adverse effects of BPA on various systems in fish models, the potential impact of parental BPA exposure on offspring pharyngeal cartilage development is poorly understood. Methods: Adult zebrafish (F0) were exposed to BPA (1.0 mu M) or control for 7 days. Eggs (F1) were collected and exposed to BPA (control, 0.05, 0.1, 1, 10 mu M) until 120 h post-fertilization. Histomorpho-metrical essay was used to quantitatively and qualitatively assess the effects of BPA on pharyngeal cartilage development. RNA sequencing (RNA-seq) was used to discover differentially expressed genes (DEGs), and KEGG pathway and GO enrichment analysis were performed to interpret functional ontology. Results: Parental BPA exposure affected hatchability and heart rates of F1 progeny. By pathology analysis, parental BPA exposure caused craniofacial deformity, characterized by wider angles of cartilage elements, disrupted pharyngeal chondrocytes and promoted apoptosis and elongation of head length. RNA-seq suggested that many DEGs were involved in multiple biological processes and signaling pathways; defense responses, reactive oxygen species metabolic process, apoptosis, p53 signaling pathway and MAPK signaling pathway were closely associated with the toxicity of parental BPA exposure. Conclusions: Parental BPA exposure affected chondrogenesis in the viscerocranium of zebrafish offspring and led to global transcriptomic changes involved in apoptosis, hyperplasia and oxidative stress. These newly identified gene expression patterns, pathways and gene networks of zebrafish eleutheroembryos after early-life waterborne BPA exposure, may lead to severe and permanent morphological and functional consequences. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页数:12
相关论文
共 67 条
  • [1] A dose-response study following in utero and lactational exposure to di-(2-ethylhexyl)-phthalate (DEHP):: Non-monotonic dose-response and low dose effects on rat brain aromatase activity
    Andrade, Anderson J. M.
    Grande, Simone W.
    Talsness, Chris E.
    Grote, Konstanze
    Chahoud, Ibrahim
    [J]. TOXICOLOGY, 2006, 227 (03) : 185 - 192
  • [2] Cardiovascular Effects and Molecular Mechanisms of Bisphenol A and Its Metabolite MBP in Zebrafish
    Brown, A. Ross
    Green, Jon M.
    Moreman, John
    Gunnarsson, Lina M.
    Mourabit, Sulayman
    Ball, Jonathan
    Winter, Matthew J.
    Trznadel, Maciej
    Correia, Ana
    Hacker, Christian
    Perry, Alexis
    Wood, Mark E.
    Hetheridge, Malcolm J.
    Currie, Richard A.
    Tyler, Charles R.
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2019, 53 (01) : 463 - 474
  • [3] The involvement of MAPK signaling pathways in determining the cellular response to p53 activation - Cell cycle arrest or apoptosis
    Brown, L
    Benchimol, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (07) : 3832 - 3840
  • [4] Induction of oxidative stress by bisphenol A in the epididymal sperm of rats
    Chitra, KC
    Latchoumycandane, C
    Mathur, PP
    [J]. TOXICOLOGY, 2003, 185 (1-2) : 119 - 127
  • [5] Modulation of estrogen causes disruption of craniofacial chondrogenesis in Danio rerio
    Cohen, Sarah P.
    LaChappelle, Adam R.
    Walker, Benjamin S.
    Lassiter, Christopher S.
    [J]. AQUATIC TOXICOLOGY, 2014, 152 : 113 - 120
  • [6] Bisphenol A alters the cardiovascular response to hypoxia in Danio rerio embryos
    Cypher, Alysha D.
    Ickes, Jessica R.
    Bagatto, Brian
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2015, 174 : 39 - 45
  • [7] MAP kinase signalling pathways in cancer
    Dhillon, A. S.
    Hagan, S.
    Rath, O.
    Kolch, W.
    [J]. ONCOGENE, 2007, 26 (22) : 3279 - 3290
  • [8] Maternal Bisphenol A exposure impaired endochondral ossification in craniofacial cartilage of rare minnow (Gobiocypris rarus) offspring
    Fan, Xiaoteng
    Wu, Lang
    Hou, Tingting
    He, Jiafa
    Wang, Cheng
    Liu, Yan
    Wang, Zaizhao
    [J]. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2018, 163 : 514 - 520
  • [9] Transcriptomic Changes in Zebrafish Embryos and Larvae Following Benzo[a]pyrene Exposure
    Fang, Xiefan
    Corrales, Jone
    Thornton, Cammi
    Clerk, Tracy
    Scheffler, Brian E.
    Willett, Kristine L.
    [J]. TOXICOLOGICAL SCIENCES, 2015, 146 (02) : 395 - 411
  • [10] Critical role of the extracellular signal-regulated kinase-MAPK pathway in osteoblast differentiation and skeletal development
    Ge, Chunxi
    Xiao, Guozhi
    Jiang, Di
    Franceschi, Renny T.
    [J]. JOURNAL OF CELL BIOLOGY, 2007, 176 (05) : 709 - 718