Characterization of a bystander effect induced by the endocrine-disrupting chemical 6-propyl-2-thiouracil in zebrafish embryos
- Authors
- Liu, C., Yan, W., Zhou, B., Guo, Y., Liu, H., Yu, H., Giesy, J.P., Wang, J., Li, G., and Zhang, X.
- ID
- ZDB-PUB-120503-3
- Date
- 2012
- Source
- Aquatic toxicology (Amsterdam, Netherlands) 118-119C: 108-115 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Albinism, Oculocutaneous/genetics
- Albinism, Oculocutaneous/metabolism
- Animals
- Blotting, Western
- Bystander Effect
- Embryo, Nonmammalian/drug effects
- Endocrine Disruptors/pharmacology*
- Gene Expression Regulation, Developmental/drug effects
- Melanins/genetics
- Melanins/metabolism
- Monophenol Monooxygenase/genetics
- Monophenol Monooxygenase/metabolism
- Propylthiouracil/pharmacology*
- RNA, Messenger/chemistry
- RNA, Messenger/genetics
- Real-Time Polymerase Chain Reaction
- Statistics, Nonparametric
- Zebrafish/embryology*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- PubMed
- 22542736 Full text @ Aquat. Toxicol.
This study was conducted to evaluate possible bystander effects induced by the model chemical 6-propyl-2-thiouracil (PTU) on melanin synthesis. Zebrafish (Danio rerio) embryos were treated with PTU by either microinjection exposure, via waterborne exposure or indirectly through bystander exposure. Melanin content, related mRNA and protein expression were examined at the end of exposure (36 h post-fertilization). Direct exposure to PTU decreased the melanin content, up-regulated mRNA expressions of oculocutaneous albinism type 2 (OCA2), tyrosinase (TYR), dopachrometautomerase (DCT), tyrosinase-related protein 1 (TYRP1) and silver (SILV), and increased the protein expressions of TYR and SILV. Bystander exposure also up-regulated mRNA and protein expressions of TYR and SILV but increased melanin contents. Correlation analysis demonstrated that mRNA expressions of OCA2, TYR, DCT, TYRP1, SILV and protein expressions of TYR and SILV in bystander exposure groups were positively correlated with corresponding expressions in microinjection exposure groups. The results might have environmental implications and highlight the need to consider the bystander effects when assessing potential risks of endocrine-disrupting chemicals.