Environmental cadmium exposure perturbs systemic iron homeostasis via hemolysis and inflammation, leading to hepatic ferroptosis in common carp (Cyprinus carpio L.)

• Published in: Ecotoxicology and environmental safety 2024-04, Vol.275, p.116246-116246, Article 116246
• Main Authors: Guo, Wenli, Zhang, Jinjin, Zhang, Xiaoqian, Ren, Quanzhong, Zheng, Guangzhe, Zhang, Jianxin, Nie, Guoxing
• Format: Article
• Language: English
• Subjects: Cadmium; Erythrocytes; Ferroptosis; Iron metabolism; Redox
• ISSN: 0147-6513; 1090-2414
• DOI: 10.1016/j.ecoenv.2024.116246

Cadmium (Cd) pollution is considered a pressing challenge to eco-environment and public health worldwide. Although it has been well-documented that Cd exhibits various adverse effects on aquatic animals, it is still largely unknown whether and how Cd at environmentally relevant concentrations affects iron metabolism. Here, we studied the effects of environmental Cd exposure (5 and 50 μg/L) on iron homeostasis and possible mechanisms in common carp. The data revealed that Cd elevated serum iron, transferrin saturation and iron deposition in livers and spleens, leading to the disruption of systemic iron homeostasis. Mechanistic investigations substantiated that Cd drove hemolysis by compromising the osmotic fragility and inducing defective morphology of erythrocytes. Cd concurrently exacerbated hepatic inflammatory responses, resulting in the activation of IL6-Stat3 signaling and subsequent hepcidin transcription. Notably, Cd elicited ferroptosis through increased iron burden and oxidative stress in livers. Taken together, our findings provide evidence and mechanistic insight that environmental Cd exposure could undermine iron homeostasis via erythrotoxicity and hepatotoxicity. Further investigation and ecological risk assessment of Cd and other pollutants on metabolism-related effects is warranted, especially under the realistic exposure scenarios. [Display omitted] •Environmental Cd exposure perturbed systemic iron homeostasis in common carp.•Cd induced hemolysis through compromising the osmotic fragility and shapes of erythrocytes.•Cd exposure exacerbated hepatic inflammatory responses, giving rise to more iron retention in tissues.•Cd elicited ferroptosis through increased iron burden and oxidative stress in livers.