Mode of action exploration of reproductive toxicity induced by bisphenol S using human normal ovarian epithelial cells through ERO-MAPK signaling pathway

被引:0
|
作者
Yu, Mengqi [1 ,2 ]
Yang, Zhirui [1 ,2 ]
Zhou, Yongru [1 ,2 ]
Guo, Wanqing [1 ,2 ]
Tian, Lin [1 ,2 ]
Zhang, Lishi [1 ,2 ]
Li, Xiaomeng [1 ,2 ,3 ]
Chen, Jinyao [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp 4, West China Sch Publ Hlth, Dept Nutr & Food Safety, Chengdu, Peoples R China
[2] Food Safety Monitoring & Risk Assessment Key Lab S, Chengdu, Peoples R China
[3] Sichuan Univ, West China Sch Publ Hlth, 16,Sect 3,Renmin South Rd, Chengdu 610041, Peoples R China
关键词
Bisphenol S; IOSE80; cells; Benchmark dose; Mode of action; ERO-MAPK signaling pathway; GONADOTROPIN-RELEASING-HORMONE; RECEPTOR GENE-EXPRESSION; ESTROGEN-RECEPTOR; UNITED-STATES; UTEROTROPHIC ASSAY; HUMAN EXPOSURE; CANCER CELLS; ANALOGS; ACTIVATION; CHEMICALS;
D O I
10.1016/j.ecoenv.2024.116037
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: In the plastics production sector, bisphenol S (BPS) has gained popularity as a replacement for bisphenol A (BPA). However, the mode of action (MOA) of female reproductive toxicity caused by BPS remains unclear and the safety of BPS is controversial. Methods: Human normal ovarian epithelial cell line, IOSE80, were exposed to BPS at human-relevant levels for short-term exposure at 24 h or 48 h, or for long-term exposure at 28 days, either alone or together with five signaling pathway inhibitors: ICI 18,2780 (estrogen receptor [ER] antagonist), G15 (GPR30 specific inhibitor), U0126 (extracellular regulated protein kinase [ERK] 1/2 inhibitor), SP600125 (c-Jun N-terminal kinase [JNK] inhibitor) or SB203580 (p38 mitogen-activated protein kinase [p38MAPK] inhibitor). MOA through ERO-MAPK signaling pathway interruption was explored, and potential thresholds were estimated by the benchmark dose method. Results: For short-term exposure, BPS exposure at human-relevant levels elevated the ESR2 and MAPK8 mRNA levels, along with the percentage of the G0/G1 phase. For long-term exposure, BPS raised the MAPK1 and EGFR mRNA levels, the ERS, p-ERK, and p-JNK protein levels, and the percentage of the G0/G1 phase, which was partly suppressed by U0126. The benchmark dose lower confidence limit (BMDL) of the percentage of the S phase after 24 h exposure was the lowest among all the BMDLs of a good fit, with BMDL5 of 9.55 mu M. Conclusions: The MOA of female reproductive toxicity caused by BPS at human-relevant levels might involve: molecular initiating event (MIE)-BPS binding to ERO receptor, key event (KE)1-the interrupted expression of GnRH, KE2-the activation of JNK (for short-term exposure) and ERK pathway (for long-term exposure), KE3-cell cycle arrest (the increased percentage of the G0/G1 phase), and KE4-interruption of cell proliferation (only for short-term exposure). The BMDL of the percentage of the S phase after 24 h exposure was the lowest among all the BMDLs of a good fit, with BMDL5 of 9.55 mu M.
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页数:11
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