The toxicity of superparamagnetic iron oxide nanoparticles induced on the testicular cells: In vitro study

NanoImpact. 2024 Jul:35:100517. doi: 10.1016/j.impact.2024.100517. Epub 2024 Jun 6.

Abstract

Superparamagnetic iron oxide nanoparticles (SPIONs) have gained significant attention in biomedical research due to their potential applications. However, little is known about their impact and toxicity on testicular cells. To address this issue, we conducted an in vitro study using primary mouse testicular cells, testis fragments, and sperm to investigate the cytotoxic effects of sodium citrate-coated SPIONs (Cit_SPIONs). Herein, we synthesized and physiochemically characterized the Cit_SPIONs and observed that the sodium citrate diminished the size and improved the stability of nanoparticles in solution during the experimental time. The sodium citrate (measured by thermogravimetry) was biocompatible with testicular cells at the used concentration (3%). Despite these favorable physicochemical properties, the in vitro experiments demonstrated the cytotoxicity of Cit_SPIONs, particularly towards testicular somatic cells and sperm cells. Transmission electron microscopy analysis confirmed that Leydig cells preferentially internalized Cit_SPIONs in the organotypic culture system, which resulted in alterations in their cytoplasmic size. Additionally, we found that Cit_SPIONs exposure had detrimental effects on various parameters of sperm cells, including motility, viability, DNA integrity, mitochondrial activity, lipid peroxidation (LPO), and ROS production. Our findings suggest that testicular somatic cells and sperm cells are highly sensitive and vulnerable to Cit_SPIONs and induced oxidative stress. This study emphasizes the potential toxicity of SPIONs, indicating significant threats to the male reproductive system. Our findings highlight the need for detailed development of iron oxide nanoparticles to enhance reproductive nanosafety.

Keywords: Nanotoxicity; Oxidative stress; SPIONs; Testicular cells; Ultrastructural alterations.

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Cells, Cultured
  • Leydig Cells / drug effects
  • Leydig Cells / metabolism
  • Lipid Peroxidation / drug effects
  • Magnetic Iron Oxide Nanoparticles* / chemistry
  • Magnetic Iron Oxide Nanoparticles* / toxicity
  • Male
  • Mice
  • Oxidative Stress / drug effects
  • Reactive Oxygen Species / metabolism
  • Sodium Citrate
  • Spermatozoa* / drug effects
  • Testis* / drug effects

Substances

  • Reactive Oxygen Species
  • Sodium Citrate