The antagonistic effect of melatonin on TBBPA‐induced apoptosis and necroptosis via PTEN/PI3K/AKT signaling pathway in swine testis cells

坏死性下垂 细胞凋亡 蛋白激酶B 四溴双酚A 褪黑素 PTEN公司 PI3K/AKT/mTOR通路 活性氧 化学 氧化应激 细胞生物学 程序性细胞死亡 半胱氨酸蛋白酶3 半胱氨酸蛋白酶 膜联蛋白 生物 生物化学 内分泌学 有机化学 阻燃剂
作者
Kexin Sun,Xu Wang,Xinyu Zhang,Xu Shi,Duqiang Gong
出处
期刊:Environmental Toxicology [Wiley]
卷期号:37 (9): 2281-2290 被引量:13
标识
DOI:10.1002/tox.23595
摘要

Abstract Tetrabromobisphenol A (TBBPA) is a widely used industrial brominated flame retardant, which can endanger animal and human health, including cytotoxicity, endocrine disruption, reproductive toxicity and so on. Melatonin (MT) is a noteworthy free radical scavenger and an antioxidant to alleviate oxidative stress. To investigate the cytotoxic of TBBPA on swine testis cells (ST cells), as well as the antagonistic effect of MT, we established TBBPA exposure and MT antagonistic models, used flow cytometry and AO/EB staining methods to detect apoptosis and necroptosis, used DCFH‐DA method to examine the content of reactive oxygen species (ROS) and investigated the expression of associated genes using RT‐PCR and Western blot. According to our findings, TBBPA exposure induced cell death in ST cells. TBBPA increased ROS levels, thus increasing PTEN expression and decreasing PI3K and AKT expression. Apoptosis‐related factors (Caspase‐3, Bax, Cyt‐c, and Caspase‐9) and necroptosis‐related factors (RIPK1, RIPK3, and MLKL) were considerably elevated, in addition to the reduced expression of BCL‐2 and Caspase‐8. We also found that MT inhibited apoptosis and necroptosis in TBBPA‐induced ST cells and effectively resolved the abnormal expression of related signaling pathways. In summary, the above results indicate that MT alleviates the disorder of PTEN/PI3K/AKT signaling pathway via inhibiting ROS overproduction, thereby mitigating apoptosis and necroptosis caused by TBBPA. This research provides a theoretical basis for further understanding of the toxicity of TBBPA and the detoxification of MT against environmental toxics.
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