Regulation of metal homeostasis and zinc transporters in early-life stage zebrafish following sublethal waterborne zinc exposure

Aquat Toxicol. 2020 Aug:225:105524. doi: 10.1016/j.aquatox.2020.105524. Epub 2020 Jun 15.

Abstract

In the present research, the effects of exposure to a sublethal concentration of zinc (Zn) on metal and ion homeostasis, and the regulation and the localization of various Zn transporters (i.e., the Zrt-Irt Like Protein (ZIP) family of Zn transporters), were investigated in zebrafish (Danio rerio) during early development. Exposure to an elevated level of Zn [4 μM (high) vs. 0.25 μM (control)] from 0 day post-fertilization (dpf) resulted in a significant increase in the whole body content of Zn at 5 dpf. A transient decrease in the whole body calcium (Ca) level was observed in 3 dpf larvae exposed to high Zn. Similarly, whole body nickel (Ni) and copper (Cu) contents were also reduced in 3 dpf larvae exposed to high Zn. Importantly, the magnitude of reduction in whole body Ni and Cu contents following Zn exposure was markedly higher than that in Ca content, suggesting that internal Ni and Cu balance were likely more sensitive to Zn exposure in developing zebrafish. Exposure to high Zn altered the mRNA expression levels of specific zip transporters, with an increase in zip1 (at 3 dpf) and zip8 (at 5 dpf), and a decrease in zip4 (at 5 dpf). The expression levels of most zip transporters tended to decrease from 3 dpf to 5 dpf with the exception of zip4 and zip8. Results from in situ hybridization revealed that several zip transporters exhibited distinct spatial distribution (e.g., zip8 in the intestinal tract, zip14 in the pronephric tubules). Overall, our findings suggested that exposure to sublethal concentrations of Zn disrupts the homeostasis of essential metals during early development and that different ZIP transporters may play unique roles in regulating Zn homeostasis in various organs in developing zebrafish.

Keywords: Calcium; Development; Metal Homeostasis; ZIP; Zebrafish; Zinc.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cation Transport Proteins / genetics*
  • Copper / metabolism
  • Dose-Response Relationship, Drug
  • Homeostasis / drug effects*
  • Larva / drug effects
  • Larva / metabolism
  • No-Observed-Adverse-Effect Level
  • Water Pollutants, Chemical / metabolism
  • Water Pollutants, Chemical / toxicity*
  • Zebrafish Proteins / genetics*
  • Zebrafish* / physiology
  • Zinc / metabolism
  • Zinc / toxicity*

Substances

  • Cation Transport Proteins
  • Water Pollutants, Chemical
  • Zebrafish Proteins
  • Copper
  • Zinc
  • Calcium