Short Chain Chlorinated Paraffins Impaired Spermatogenesis Process in Mice via Inhibiting α-KG/TET Enzyme Activity.
Ruiyang MengXingde DuYu FuFufang WangYingfei YangFeiyang GuoXin WangKangfeng GeJun YangXiao LiangHongxiang GuoWenjun WangXiaodong LiuHuizhen ZhangPublished in: Environmental science & technology (2024)
Short chain chlorinated paraffins (SCCPs) are widely found in various environmental media and potentially threaten human health. However, the toxicity mechanisms of SCCPs to the male reproductive system remain unclear. In this study, male BALB/c mice and GC-1 cells were used to investigate the reproductive toxicity of SCCPs and their molecular mechanisms. SCCPs decreased the content of the tricarboxylic acid cycle intermediate α-KG in testicular cells, thus inhibiting the activity of the DNA demethylase TET enzyme and resulting in an increase in the overall methylation level of the testicular genome. Correspondingly, the promoter demethylation and expression of spermatogenesis-related genes Rbm46 , Sohlh1 , Kit , and Dmrt1 were significantly reduced by SCCPs, which further prevented the transformation of spermatogonia to spermatocytes and reduced sperm quality in mice. The in vitro experiments suggested that the TGFβ pathway activated by oxidative stress might be an essential reason for inhibiting the tricarboxylic acid cycle and the reduction of α-KG content in testicular cells induced by SCCPs. Overall, this study reveals a novel metabolic regulatory mechanism of SCCPs-induced spermatogenesis disorders, which provides an essential theoretical basis for the prevention of reproductive toxicity of SCCPs.
Keyphrases
- induced apoptosis
- oxidative stress
- human health
- signaling pathway
- cell cycle arrest
- risk assessment
- diabetic rats
- dna methylation
- transcription factor
- high fat diet induced
- endoplasmic reticulum stress
- dna damage
- gene expression
- cell death
- type diabetes
- insulin resistance
- mass spectrometry
- pi k akt
- high glucose
- heat stress
- binding protein
- simultaneous determination