Folic Acid Alleviates Hydrogen Peroxide-Induced Oxidative Stress in Bovine Placental Trophoblast Cells by Regulating the NRF2/mTOR Signaling Pathway.

IF 4.9 2区 生物学 International Journal of Molecular Sciences Pub Date : 2025-03-20 DOI:10.3390/ijms26062818
Liyuan Shi, Zhisheng Wang, Jianxin Xiao, Rui Hu, Huawei Zou, Junmei Wang, Ziqi Yue, Quanhui Peng, Yahui Jiang, Bai Xue, Lizhi Wang
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Abstract

As one of the important components of placental structure, the integrity of placental trophoblast cells is crucial for placental function. When oxidative stress continues to act on placental trophoblast cells, it can cause changes in placental structure and function. Research has shown that folic acid (FA) has a certain alleviating effect on the functional damage of trophoblast cells caused by oxidative stress, but the mechanism of action is still unclear. Therefore, this study focuses on bovine placental trophoblast cells (BPTCs) to explore the effects and mechanisms by which FA regulates oxidative stress in cells, with the aim of providing a theoretical foundation for improving the reproductive performance of cows. The results show that, compared with the H2O2 group, the FA+ H2O2 group showed an increase in the cell proliferation index (PI), superoxide dismutase 2 (SOD2), glutathione peroxidase (GSH-px), and catalase (CAT) mRNA expression and total antioxidant capacity (T-AOC) of cells, while the content of reactive oxygen species (ROS) decreased. In addition, the mRNA expression of tight junction factors, nutrient transporters, placental functional factors, mammalian rapamycin (mTOR) and its downstream factors, and nuclear factor erythroid 2-related factor 2 (NRF2) and its downstream factors in the FA+ H2O2 group increased, while the protein abundance of nuclear NRF2 decreased. After treatment with the inhibitor ML385, it was found that the protective effect of FA on H2O2-induced cellular oxidative damage was alleviated. These results indicate that FA can regulate the NRF2/mTOR signaling pathway, promote the expression of antioxidant factors, and alleviate the damage to the cell barrier and nutrient transport function in BPTCs caused by oxidative stress.

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叶酸通过调控NRF2/mTOR信号通路缓解过氧化氢诱导的牛胎盘滋养细胞氧化应激
胎盘滋养细胞作为胎盘结构的重要组成部分之一,其完整性对胎盘的功能至关重要。当氧化应激持续作用于胎盘滋养细胞时,可引起胎盘结构和功能的改变。研究表明,叶酸(folic acid, FA)对氧化应激引起的滋养细胞功能损伤有一定的缓解作用,但其作用机制尚不清楚。因此,本研究以牛胎盘滋养细胞(BPTCs)为研究对象,探讨FA对细胞氧化应激的调控作用及其机制,以期为提高奶牛繁殖性能提供理论依据。结果表明,与H2O2组相比,FA+ H2O2组细胞增殖指数(PI)、超氧化物歧化酶2 (SOD2)、谷胱甘肽过氧化物酶(GSH-px)、过氧化氢酶(CAT) mRNA表达量和细胞总抗氧化能力(T-AOC)升高,活性氧(ROS)含量降低;此外,FA+ H2O2组紧密连接因子、营养转运蛋白、胎盘功能因子、哺乳动物雷帕霉素(mTOR)及其下游因子、核因子红系2相关因子2 (NRF2)及其下游因子mRNA表达量升高,核NRF2蛋白丰度降低。经抑制剂ML385处理后,发现FA对h2o2诱导的细胞氧化损伤的保护作用有所减轻。上述结果表明,FA可调节NRF2/mTOR信号通路,促进抗氧化因子的表达,减轻氧化应激对bptc细胞屏障和营养转运功能的损害。
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10.70%
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13472
审稿时长
1.7 months
期刊介绍: The International Journal of Molecular Sciences (ISSN 1422-0067) provides an advanced forum for chemistry, molecular physics (chemical physics and physical chemistry) and molecular biology. It publishes research articles, reviews, communications and short notes. Our aim is to encourage scientists to publish their theoretical and experimental results in as much detail as possible. Therefore, there is no restriction on the length of the papers or the number of electronics supplementary files. For articles with computational results, the full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material (including animated pictures, videos, interactive Excel sheets, software executables and others).
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