Effects of Zearalenone on Apoptosis and Copper Accumulation of Goat Granulosa Cells In Vitro.
Liang LiuJianyu MaZongyou WeiYingnan YangDongxu LiYongjie WanPublished in: Biology (2023)
Zearalenone (ZEA), also known as F-2 toxin, is a mycotoxin. Despite numerous reports of ZEA impairing livestock production performance and fertility, little information is available, including information about the mechanism underlying damage to cell metal ion transport. Copper, which is essential for cell survival as a metal ion, can consist of a variety of enzymes that facilitate abundant metabolic processes. However, the accumulation of copper in cells can have toxic effects. Here, we intended to determine whether ZEA could impair goat granulosa cells (GCs) and alter the cellular copper concentration. GCs were divided into a negative control (NC) group (cells cultured with 0.1% dimethyl sulfoxide (DMSO) for 8 h) and a ZEA group (cells cultured with 200 μmol/L ZEA diluted in DMSO for 8 h). The results showed that ZEA could inhibit GC proliferation and impair cell viability. GCs showed significant increases in the apoptosis rate and oxidative stress levels, while their ability to synthesize estrogen decreased. In addition, RNA-seq results showed dramatic changes in the expression of copper transport-related genes. The expression levels of ATPase copper transporting alpha ( ATP7A ) and ATPase copper transporting beta ( ATP7B ) were significantly downregulated ( p < 0.01), while the expression of solute carrier family 31 member 1 ( SLC31A1 ) was not modified in the ZEA group compared with the NC group. In accordance with these trends, the copper concentration increased significantly in the ZEA group ( p < 0.01). In summary, our results show that ZEA can negatively affect GCs and cause copper accumulation. This finding may provide a prospective line of research on the relationship between ZEA and the transport of copper ions in GCs.
Keyphrases
- induced apoptosis
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- oxide nanoparticles
- cell death
- rna seq
- single cell
- poor prognosis
- escherichia coli
- signaling pathway
- emergency department
- metabolic syndrome
- mesenchymal stem cells
- binding protein
- quantum dots
- young adults
- insulin resistance
- skeletal muscle
- drug induced
- solid phase extraction