4.5 Article

Evaluation of the cytotoxic activity of triphenyl phosphate on mouse spermatocytes cells

Journal

TOXICOLOGY IN VITRO
Volume 90, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tiv.2023.105607

Keywords

TPhP; Oxidative stress; Mitochondrial impairment; DNA damage; Mitochondria-dependent apoptosis

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Triphenyl phosphate (TPhP) is commonly present in the environment and general population as an organophosphorus flame retardant. This study investigated the direct effects of TPhP on the growth and development of sperm cells. Results showed that TPhP treatment decreased cell viability and induced apoptosis in a dose-dependent manner. It also increased intracellular reactive oxygen species and DNA damage. Furthermore, TPhP altered mitochondrial structure and function, leading to caspase-3 dependent apoptosis. These findings suggest that TPhP has reproductive toxicity and caution should be taken.
Triphenyl phosphate (TPhP) is one of the most commonly found organophosphorus flame retardants (OPFRs) in the environment and the general population. Continuous daily exposure to TPhP may adversely impact male reproductive health. However, few researches were conducted to investigate the direct effects of TPhP on the progress of sperm growth and development. In this study, mouse spermatocyte GC-2spd (GC-2) cells were selected as an in vitro model, the impact of oxidative stress, mitochondrial impairment, DNA damage, cell apoptosis and the related molecular mechanisms were investigated using high content screening (HCS) system. Our study indicated that cell viability was decreased significantly in a dose-dependent manner after TPhP treatment with the half lethal concentration (LC50) at 105.8, 61.61 and 53.23 mu M for 24, 48 and 72 h. A concentration-related apoptosis occurrence was observed in GC-2 cells after TPhP exposure for 48 h. In addition, the elevated intracellular reactive oxygen species (ROS) and the total antioxidant capacity (T-AOC) also observed after exposing to 6, 30 and 60 mu M of TPhP. Furthermore, based on the enhancement of pH2AX protein and alteration of nuclear morphology or DNA content, DNA damage might be induced by higher concentration of TPhP treatment. Simultaneously, alteration of mitochondrial structure, enhancement of mitochondrial membrane potential (MMP), reduction of cellular adenosine triphosphate (ATP) content, altered expression of Bcl-2 family proteins, release of cytochrome c and increase of caspase-3 and caspase-9 activity demonstrated that caspase-3 dependent mitochondrial pathway might play a key role in the process of GC-2 cell apoptosis. Taken together, these results showed that TPhP was a mitochondrial toxicant and apoptotic inducer, which might trigger alike responses in human spermatogenic cells. Therefore, the potential reproductive toxicity of TPhP should not be ignored.

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