1. Academic Validation
  2. Effect of bisphenol A on craniofacial cartilage development in zebrafish (Danio rerio) embryos: A morphological study

Effect of bisphenol A on craniofacial cartilage development in zebrafish (Danio rerio) embryos: A morphological study

  • Ecotoxicol Environ Saf. 2021 Apr 1:212:111991. doi: 10.1016/j.ecoenv.2021.111991.
Wenlong Huang 1 Xin Wang 1 Shukai Zheng 1 Ruotong Wu 2 Caixia Liu 1 Kusheng Wu 3
Affiliations

Affiliations

  • 1 Department of Preventive Medicine, Shantou University Medical College, Shantou 515041, Guangdong, China.
  • 2 School of Life Science, Xiamen University, Xiamen 361102, Fujian, China.
  • 3 Department of Preventive Medicine, Shantou University Medical College, Shantou 515041, Guangdong, China; Guangdong Provincial Key Laboratory of Breast Cancer Diagnosis and Treatment, Shantou 515041, Guangdong, China. Electronic address: [email protected].
Abstract

Bisphenol A (BPA), an endocrine-disrupting chemical, is present in everyday-used consumables and common household products. Although the side effects of BPA have been sufficiently explored, little is known the effects of environmentally relevant low levels of BPA on chondrogenesis in skeletal development. Here we used a morphological approach to investigate whether exposure to BPA (0, 0.0038, 0.05, 0.1, 1.0 μM) could affect craniofacial cartilage development of zebrafish embryo. Furthermore, we sought to determine receptor-mediated BPA induced chondrogenesis toxicity by co-exposing developing embryos to BPA and various inhibitors. Low-dose BPA affected heart rate and induced body and head elongation of larvae. Quantitative morphometric and histopathological analysis revealed that BPA exposure changed the angle and length of craniofacial cartilage elements and disrupted chondrocytes. BPA induced pharyngeal cartilage defects via multiple cellular pathways, including Estrogen receptor, Androgen Receptor, and estrogen-related receptors. Our findings demonstrate that BPA alters the normal development of cartilage and craniofacial structures in zebrafish embryos. Furthermore, in this study we find multiple cellular pathways mediating the effects of BPA-induced craniofacial chondrogenesis toxicity. Further experiments will allow for establishing a connection between BPA and increased risk of congenital malformation of the facial cranium in BPA-exposed populations.

Keywords

Bisphenol A; Craniofacial cartilage development; Developmental toxicity; Endocrine-disrupting chemical; Zebrafish.

Figures
Products