Zhu Xiliang, Liu Qi, Cheng Zhaoyun, Luo Yi
Department of Cardiovascular Surgery, Central China Subcenter of National Center for Cardiovascular Diseases, Henan Cardiovascular Disease Center, Fuwai Central-China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, China.
Department of Cardiology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
J Cell Mol Med. 2025 May;29(9):e70416. doi: 10.1111/jcmm.70416.
Bisphenol A (BPA) is a widely used industrial chemical with potential endocrine-disrupting effects on metabolic processes. This study investigates the impact of BPA on hepatic function and transcriptional regulation in mouse livers and AML12 cells. Male mice were exposed to low (5 g/kg) and high (50 g/kg) doses of BPA for six weeks. Transcriptomic analysis was performed on liver tissues, and histological examinations were conducted. AML12 cells were treated with varying BPA concentrations, and PPARG transcriptional activity was assessed using a luciferase reporter assay. Additionally, molecular docking, molecular dynamics (MD) simulations, drug affinity responsive target stability (DARTS), cellular thermal shift assay (CETSA), MM-PBSA calculations, and multi-species protein structure comparative analysis were employed to analyse the interaction between BPA and PPARG. Transcriptomic analysis revealed a decrease in differentially expressed genes with higher BPA doses, with low-dose exposure significantly downregulating hepatic Cpt1a mRNA levels. Histological examination indicated lipid vacuole formation at high doses without collagen deposition. BPA consistently inhibited PPARG activity in both MCF7 cells and mouse livers. BPA exposure disrupts hepatic lipid metabolism and PPARG activity, highlighting its role as an endocrine disruptor. Further research is needed to elucidate the long-term effects of BPA on liver health.
双酚A(BPA)是一种广泛使用的工业化学品,对代谢过程具有潜在的内分泌干扰作用。本研究调查了BPA对小鼠肝脏和AML12细胞的肝功能及转录调控的影响。雄性小鼠分别暴露于低剂量(5 μg/kg)和高剂量(50 μg/kg)的BPA中六周。对肝脏组织进行转录组分析,并进行组织学检查。用不同浓度的BPA处理AML12细胞,并使用荧光素酶报告基因测定法评估PPARG的转录活性。此外,采用分子对接、分子动力学(MD)模拟、药物亲和力响应靶点稳定性(DARTS)、细胞热位移分析(CETSA)、MM-PBSA计算和多物种蛋白质结构比较分析来分析BPA与PPARG之间的相互作用。转录组分析显示,随着BPA剂量的增加,差异表达基因减少,低剂量暴露显著下调肝脏Cpt1a mRNA水平。组织学检查表明,高剂量时会形成脂质空泡,且无胶原沉积。BPA在MCF7细胞和小鼠肝脏中均持续抑制PPARG活性。BPA暴露会破坏肝脏脂质代谢和PPARG活性,突出了其作为内分泌干扰物的作用。需要进一步研究以阐明BPA对肝脏健康的长期影响。