Manganese-induced miR-125b-2-3p promotes anxiety-like behavior via TFR1-mediated ferroptosis

Environ Pollut. 2024 Mar 1:344:123255. doi: 10.1016/j.envpol.2023.123255. Epub 2023 Dec 28.

Abstract

The toxic effects of excessive manganese (Mn) levels in the environment have led to a severe public health concern. Ferroptosis is a newly form of cell death relying on iron, inherent to pathophysiological processes of psychiatric disorders, such as anxiety and depression-like behaviors. Excessive Mn exposure causes various neurological effects, including neuronal death and mood disorders. Whether Mn exposure causes anxiety and depression-like behaviors, and the underlying mechanisms of Mn-induced ferroptosis have yet to be determined. Here, Mn-exposed mice showed anxiety-like behavior. We also confirmed the accumulation of ferrous ion (Fe2+), lipid peroxidation, and depletion of antioxidant defense system both in vitro and in vivo Mn-exposed models, suggesting that Mn exposure can induce ferroptosis. Furthermore, Mn exposure downregulated the expression of miR-125b-2-3p. In turn, overexpression of miR-125b-2-3p alleviated the Mn-induced ferroptosis by targeting Transferrin receptor protein 1 (TFR1). In summary, this novel study established the propensity of Mn to cause anxiety-like behavior, an effect that was regulated by miR-125b-2-3p and ensuing ferroptosis secondary to the targeting of TFR1. These results offer promising targets for the prevention and treatment of Mn-induced neurotoxicity.

Keywords: Anxiety; Ferroptosis; Manganese; MiR-125b-2-3p; TFR1.

MeSH terms

  • Animals
  • Anxiety / chemically induced
  • Ferroptosis*
  • Humans
  • Iron / toxicity
  • Manganese / toxicity
  • Mice
  • MicroRNAs*
  • Receptors, Transferrin / genetics

Substances

  • Manganese
  • Iron
  • Receptors, Transferrin
  • MicroRNAs