Zinc supplementation protects against cadmium accumulation and cytotoxicity in Madin-Darby bovine kidney cells

PLoS One. 2014 Aug 8;9(8):e103427. doi: 10.1371/journal.pone.0103427. eCollection 2014.

Abstract

Cadmium ions (Cd2+) have been reported to accumulate in bovine tissues, although Cd2+ cytotoxicity has not been investigated thoroughly in this species. Zinc ions (Zn2+) have been shown to antagonize the toxic effects of heavy metals such as Cd2+ in some systems. The present study investigated Cd2+ cytotoxicity in Madin-Darby bovine kidney (MDBK) epithelial cells, and explored whether this was modified by Zn2+. Exposure to Cd2+ led to a dose- and time-dependent increase in apoptotic cell death, with increased intracellular levels of reactive oxygen species and mitochondrial damage. Zn2+ supplementation alleviated Cd2+-induced cytotoxicity and this protective effect was more obvious when cells were exposed to a lower concentration of Cd2+ (10 μM), as compared to 50 μM Cd2+. This indicated that high levels of Cd2+ accumulation might induce irreversible damage in bovine kidney cells. Metallothioneins (MTs) are metal-binding proteins that play an essential role in heavy metal ion detoxification. We found that co-exposure to Zn2+ and Cd2+ synergistically enhanced RNA and protein expression of MT-1, MT-2, and the metal-regulatory transcription factor 1 in MDBK cells. Notably, addition of Zn2+ reduced the amounts of cytosolic Cd2+ detected following MDBK exposure to 10 μM Cd2+. These findings revealed a protective role of Zn2+ in counteracting Cd2+ uptake and toxicity in MDBK cells, indicating that this approach may provide a means to protect livestock from excessive Cd2+ accumulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cadmium / pharmacokinetics*
  • Cadmium / toxicity*
  • Cattle
  • Cell Line
  • Dietary Supplements
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects*
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Metallothionein / metabolism
  • Time Factors
  • Zinc / administration & dosage
  • Zinc / pharmacology*

Substances

  • Cadmium
  • Metallothionein
  • Zinc

Grants and funding

This study was supported by the Fundamental Research Funds for the Central Universities, Huazhong Agricultural University Scientific & Technological Self-innovation Foundation, and the Chinese Agricultural Research Systems (CARS-38). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.