HIF-1α/ ho -1介导的铁凋亡参与聚苯乙烯纳米塑料诱导的代际心脏毒性

IF 9.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ruiqiong Li, Xifeng Wang, Jinjin Zhang, Yinchu Hu, Yuxin Yang, Ying Zhang, Boqing Li, Meidi Shen, Chongkun Wang, Yuanyuan Yang, Xiaodong Song*, Lihua Ren* and Lianshuang Zhang*, 
{"title":"HIF-1α/ ho -1介导的铁凋亡参与聚苯乙烯纳米塑料诱导的代际心脏毒性","authors":"Ruiqiong Li,&nbsp;Xifeng Wang,&nbsp;Jinjin Zhang,&nbsp;Yinchu Hu,&nbsp;Yuxin Yang,&nbsp;Ying Zhang,&nbsp;Boqing Li,&nbsp;Meidi Shen,&nbsp;Chongkun Wang,&nbsp;Yuanyuan Yang,&nbsp;Xiaodong Song*,&nbsp;Lihua Ren* and Lianshuang Zhang*,&nbsp;","doi":"10.1021/acs.nanolett.4c0537210.1021/acs.nanolett.4c05372","DOIUrl":null,"url":null,"abstract":"<p >To explore the intergenerational cardiotoxicity of nanoplastics, maternal mice were exposed to 60 nm polystyrene nanoplastics (PS-NP) during pregnancy and lactation. The results showed that PS-NP can enter the hearts of offspring and induce myocardial fiber arrangement disorder, acidophilic degeneration of cardiomyocytes, and elevated creatine kinase isoenzymes (CK-MB) and lactate dehydrogenase (LDH) levels after maternal exposure to PS-NP at 100 mg/kg during pregnancy and lactation. Mechanistically, KEGG analysis of RNA sequencing showed the participation of hypoxia-inducible factor-1 (HIF-1) and ferroptosis in PS-NP-induced cardiotoxicity. Key features of ferroptosis, including Fe<sup>2+</sup> accumulation, mitochondrial injury, oxidative stress, GPX4 downregulation, and FTH1, ACSL4, and SLC7A11 upregulation, were detected. Furthermore, PS-NP treatment upregulated the expressions of HIF-1α and HO-1, and PS-NP-induced ferroptosis can be alleviated by inhibition of HIF-1α using si-HIF-1α. This study provided an insightful reference for the intergenerational cardiotoxicity assessment of PS-NP.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"25 6","pages":"2226–2235 2226–2235"},"PeriodicalIF":9.1000,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HIF-1α/HO-1-Mediated Ferroptosis Participates in Polystyrene Nanoplastics-Induced Intergenerational Cardiotoxicity\",\"authors\":\"Ruiqiong Li,&nbsp;Xifeng Wang,&nbsp;Jinjin Zhang,&nbsp;Yinchu Hu,&nbsp;Yuxin Yang,&nbsp;Ying Zhang,&nbsp;Boqing Li,&nbsp;Meidi Shen,&nbsp;Chongkun Wang,&nbsp;Yuanyuan Yang,&nbsp;Xiaodong Song*,&nbsp;Lihua Ren* and Lianshuang Zhang*,&nbsp;\",\"doi\":\"10.1021/acs.nanolett.4c0537210.1021/acs.nanolett.4c05372\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >To explore the intergenerational cardiotoxicity of nanoplastics, maternal mice were exposed to 60 nm polystyrene nanoplastics (PS-NP) during pregnancy and lactation. The results showed that PS-NP can enter the hearts of offspring and induce myocardial fiber arrangement disorder, acidophilic degeneration of cardiomyocytes, and elevated creatine kinase isoenzymes (CK-MB) and lactate dehydrogenase (LDH) levels after maternal exposure to PS-NP at 100 mg/kg during pregnancy and lactation. Mechanistically, KEGG analysis of RNA sequencing showed the participation of hypoxia-inducible factor-1 (HIF-1) and ferroptosis in PS-NP-induced cardiotoxicity. Key features of ferroptosis, including Fe<sup>2+</sup> accumulation, mitochondrial injury, oxidative stress, GPX4 downregulation, and FTH1, ACSL4, and SLC7A11 upregulation, were detected. Furthermore, PS-NP treatment upregulated the expressions of HIF-1α and HO-1, and PS-NP-induced ferroptosis can be alleviated by inhibition of HIF-1α using si-HIF-1α. This study provided an insightful reference for the intergenerational cardiotoxicity assessment of PS-NP.</p>\",\"PeriodicalId\":53,\"journal\":{\"name\":\"Nano Letters\",\"volume\":\"25 6\",\"pages\":\"2226–2235 2226–2235\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2025-01-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nano Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.nanolett.4c05372\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.nanolett.4c05372","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

为了探讨纳米塑料的代际心脏毒性,母鼠在怀孕和哺乳期间暴露于60 nm聚苯乙烯纳米塑料(PS-NP)。结果表明,妊娠和哺乳期母亲以100 mg/kg剂量暴露于PS-NP后,PS-NP可进入子代心脏,引起心肌纤维排列紊乱、心肌细胞嗜酸变性、肌酸激酶同工酶(CK-MB)和乳酸脱氢酶(LDH)水平升高。在机制上,RNA测序的KEGG分析显示缺氧诱导因子-1 (HIF-1)和铁凋亡参与了ps - np诱导的心脏毒性。检测铁下沉的关键特征,包括Fe2+积累、线粒体损伤、氧化应激、GPX4下调以及FTH1、ACSL4和SLC7A11上调。此外,PS-NP处理可上调HIF-1α和HO-1的表达,si-HIF-1α可通过抑制HIF-1α减轻PS-NP诱导的铁下垂。本研究为PS-NP的代际心脏毒性评估提供了有意义的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HIF-1α/HO-1-Mediated Ferroptosis Participates in Polystyrene Nanoplastics-Induced Intergenerational Cardiotoxicity

HIF-1α/HO-1-Mediated Ferroptosis Participates in Polystyrene Nanoplastics-Induced Intergenerational Cardiotoxicity

To explore the intergenerational cardiotoxicity of nanoplastics, maternal mice were exposed to 60 nm polystyrene nanoplastics (PS-NP) during pregnancy and lactation. The results showed that PS-NP can enter the hearts of offspring and induce myocardial fiber arrangement disorder, acidophilic degeneration of cardiomyocytes, and elevated creatine kinase isoenzymes (CK-MB) and lactate dehydrogenase (LDH) levels after maternal exposure to PS-NP at 100 mg/kg during pregnancy and lactation. Mechanistically, KEGG analysis of RNA sequencing showed the participation of hypoxia-inducible factor-1 (HIF-1) and ferroptosis in PS-NP-induced cardiotoxicity. Key features of ferroptosis, including Fe2+ accumulation, mitochondrial injury, oxidative stress, GPX4 downregulation, and FTH1, ACSL4, and SLC7A11 upregulation, were detected. Furthermore, PS-NP treatment upregulated the expressions of HIF-1α and HO-1, and PS-NP-induced ferroptosis can be alleviated by inhibition of HIF-1α using si-HIF-1α. This study provided an insightful reference for the intergenerational cardiotoxicity assessment of PS-NP.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Nano Letters
Nano Letters 工程技术-材料科学:综合
CiteScore
16.80
自引率
2.80%
发文量
1182
审稿时长
1.4 months
期刊介绍: Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including: - Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale - Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies - Modeling and simulation of synthetic, assembly, and interaction processes - Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance - Applications of nanoscale materials in living and environmental systems Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信