Jing-Ai Li , Li-Qing Wang , Qiong-Jun Xu , Xiao-Mei Wu , Xiao-Qing Pang , Jin-Xin He , Qian-Feng Qiao , Huang-Nian You , Yan-Chun Wu , Yong-Jiang Zhou
{"title":"聚苯乙烯纳米塑料通过细胞周期阻滞和JNK-MAPK途径介导的氧化应激损害早期妊娠小鼠子宫内膜脱胞化","authors":"Jing-Ai Li , Li-Qing Wang , Qiong-Jun Xu , Xiao-Mei Wu , Xiao-Qing Pang , Jin-Xin He , Qian-Feng Qiao , Huang-Nian You , Yan-Chun Wu , Yong-Jiang Zhou","doi":"10.1016/j.fct.2025.115707","DOIUrl":null,"url":null,"abstract":"<div><div>The ubiquitous polystyrene nanoplastics (PS-NPs) in the environment have emerged as a significant public health concern. Their biological safety, particularly their impact on female fertility, has garnered increasing attention. Our previous study demonstrated that PS-NPs impaired endometrial decidualization. However, the underlying mechanism remains unclear. In this study, we explored the underlying mechanism by which PS-NPs compromised decidualization in early pregnant mice. Our results showed that PS-NPs disrupted uterine decidualization. Specifically, PS-NPs inhibited endometrial cell proliferation and hindered the formation of decidual polyploid cells. Additionally, PS-NPs induced oxidative damage in uteri by disrupting the balance between oxidative stress and antioxidative defenses in the decidua. PS-NPs interfered with the formation of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes, ultimately impairing cell cycle progression at the G1-S and G2-M phases. Inhibition of the JNK-MAPK pathway alleviated excessive oxidative stress in uteri, restored defective decidualization, and improved embryo implantation in PS-NPs-exposed pregnant mice. Further analysis revealed that the JNK-MAPK pathway mediated the PS-NPs-induced suppression of endometrial proliferation. These findings suggested that impaired endometrial proliferation driven by reduced activity of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes may be an important contributor to PS-NPs-induced decidualization defect. Moreover, the JNK-MAPK pathways may be mediators of these detrimental effects.</div></div>","PeriodicalId":317,"journal":{"name":"Food and Chemical Toxicology","volume":"205 ","pages":"Article 115707"},"PeriodicalIF":3.5000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polystyrene nanoplastics impair endometrial decidualization via cell cycle arrest and JNK-MAPK pathway-mediated oxidative stress in early pregnant mice\",\"authors\":\"Jing-Ai Li , Li-Qing Wang , Qiong-Jun Xu , Xiao-Mei Wu , Xiao-Qing Pang , Jin-Xin He , Qian-Feng Qiao , Huang-Nian You , Yan-Chun Wu , Yong-Jiang Zhou\",\"doi\":\"10.1016/j.fct.2025.115707\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The ubiquitous polystyrene nanoplastics (PS-NPs) in the environment have emerged as a significant public health concern. Their biological safety, particularly their impact on female fertility, has garnered increasing attention. Our previous study demonstrated that PS-NPs impaired endometrial decidualization. However, the underlying mechanism remains unclear. In this study, we explored the underlying mechanism by which PS-NPs compromised decidualization in early pregnant mice. Our results showed that PS-NPs disrupted uterine decidualization. Specifically, PS-NPs inhibited endometrial cell proliferation and hindered the formation of decidual polyploid cells. Additionally, PS-NPs induced oxidative damage in uteri by disrupting the balance between oxidative stress and antioxidative defenses in the decidua. PS-NPs interfered with the formation of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes, ultimately impairing cell cycle progression at the G1-S and G2-M phases. Inhibition of the JNK-MAPK pathway alleviated excessive oxidative stress in uteri, restored defective decidualization, and improved embryo implantation in PS-NPs-exposed pregnant mice. Further analysis revealed that the JNK-MAPK pathway mediated the PS-NPs-induced suppression of endometrial proliferation. These findings suggested that impaired endometrial proliferation driven by reduced activity of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes may be an important contributor to PS-NPs-induced decidualization defect. Moreover, the JNK-MAPK pathways may be mediators of these detrimental effects.</div></div>\",\"PeriodicalId\":317,\"journal\":{\"name\":\"Food and Chemical Toxicology\",\"volume\":\"205 \",\"pages\":\"Article 115707\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food and Chemical Toxicology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0278691525004752\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food and Chemical Toxicology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0278691525004752","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
Polystyrene nanoplastics impair endometrial decidualization via cell cycle arrest and JNK-MAPK pathway-mediated oxidative stress in early pregnant mice
The ubiquitous polystyrene nanoplastics (PS-NPs) in the environment have emerged as a significant public health concern. Their biological safety, particularly their impact on female fertility, has garnered increasing attention. Our previous study demonstrated that PS-NPs impaired endometrial decidualization. However, the underlying mechanism remains unclear. In this study, we explored the underlying mechanism by which PS-NPs compromised decidualization in early pregnant mice. Our results showed that PS-NPs disrupted uterine decidualization. Specifically, PS-NPs inhibited endometrial cell proliferation and hindered the formation of decidual polyploid cells. Additionally, PS-NPs induced oxidative damage in uteri by disrupting the balance between oxidative stress and antioxidative defenses in the decidua. PS-NPs interfered with the formation of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes, ultimately impairing cell cycle progression at the G1-S and G2-M phases. Inhibition of the JNK-MAPK pathway alleviated excessive oxidative stress in uteri, restored defective decidualization, and improved embryo implantation in PS-NPs-exposed pregnant mice. Further analysis revealed that the JNK-MAPK pathway mediated the PS-NPs-induced suppression of endometrial proliferation. These findings suggested that impaired endometrial proliferation driven by reduced activity of CyclinD1-Cdk4, CyclinE1-Cdk2, CyclinA1-Cdk2, and CyclinB1-Cdk1 complexes may be an important contributor to PS-NPs-induced decidualization defect. Moreover, the JNK-MAPK pathways may be mediators of these detrimental effects.
期刊介绍:
Food and Chemical Toxicology (FCT), an internationally renowned journal, that publishes original research articles and reviews on toxic effects, in animals and humans, of natural or synthetic chemicals occurring in the human environment with particular emphasis on food, drugs, and chemicals, including agricultural and industrial safety, and consumer product safety. Areas such as safety evaluation of novel foods and ingredients, biotechnologically-derived products, and nanomaterials are included in the scope of the journal. FCT also encourages submission of papers on inter-relationships between nutrition and toxicology and on in vitro techniques, particularly those fostering the 3 Rs.
The principal aim of the journal is to publish high impact, scholarly work and to serve as a multidisciplinary forum for research in toxicology. Papers submitted will be judged on the basis of scientific originality and contribution to the field, quality and subject matter. Studies should address at least one of the following:
-Adverse physiological/biochemical, or pathological changes induced by specific defined substances
-New techniques for assessing potential toxicity, including molecular biology
-Mechanisms underlying toxic phenomena
-Toxicological examinations of specific chemicals or consumer products, both those showing adverse effects and those demonstrating safety, that meet current standards of scientific acceptability.
Authors must clearly and briefly identify what novel toxic effect (s) or toxic mechanism (s) of the chemical are being reported and what their significance is in the abstract. Furthermore, sufficient doses should be included in order to provide information on NOAEL/LOAEL values.