基于人体细胞模型的人体消费品中微塑料的毒性比较。

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Food and Chemical Toxicology Pub Date : 2025-02-01 DOI:10.1016/j.fct.2024.115194
Alisha Janiga-MacNelly , Tham C. Hoang , Ramon Lavado
{"title":"基于人体细胞模型的人体消费品中微塑料的毒性比较。","authors":"Alisha Janiga-MacNelly ,&nbsp;Tham C. Hoang ,&nbsp;Ramon Lavado","doi":"10.1016/j.fct.2024.115194","DOIUrl":null,"url":null,"abstract":"<div><div>Originally developed to conserve natural resources, plastic has become a global pollution issue due to inadequate waste management. The dispersion and weathering of plastic waste in the environment generate micro-sized particles. Despite extensive research on the toxicological effects of pristine polymers, the impact of microplastics (MPs) from consumer plastics is poorly understood. This study investigated the cytotoxic and genotoxic effects of cryo-milled single-use plastic products (fork and cup) on eight cell lines (Caco-2, HEK001, MRC-5, HMEC-1, HepaRG, HMC-3, and T47D) at concentrations from 0.01 to 100 μg/mL. Results showed that 100 μg/mL of MPs did not significantly affect cell viability in Caco-2, HEK001, MRC-5, and T47D. However, HMEC-1 and HMC-3 exhibited decreased viability with 10–100 μg/mL of fork particles, while HMC-3 and HepaRG showed reduced viability with 100 μg/mL of cup particles. Conversely, cup particles increased HMEC-1 proliferation at 0.1–100 μg/mL. Comet assay data indicated that both fork and cup exposure led to elevated DNA fragmentation in HMEC-1 and HMC-3 cells. These findings indicate that MPs from consumer-grade plastics may exhibit cytotoxic and genotoxic effects, with endothelial and microglial cells being particularly susceptible.</div></div>","PeriodicalId":317,"journal":{"name":"Food and Chemical Toxicology","volume":"196 ","pages":"Article 115194"},"PeriodicalIF":3.9000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative toxicity of microplastics obtained from human consumer products on human cell-based models\",\"authors\":\"Alisha Janiga-MacNelly ,&nbsp;Tham C. Hoang ,&nbsp;Ramon Lavado\",\"doi\":\"10.1016/j.fct.2024.115194\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Originally developed to conserve natural resources, plastic has become a global pollution issue due to inadequate waste management. The dispersion and weathering of plastic waste in the environment generate micro-sized particles. Despite extensive research on the toxicological effects of pristine polymers, the impact of microplastics (MPs) from consumer plastics is poorly understood. This study investigated the cytotoxic and genotoxic effects of cryo-milled single-use plastic products (fork and cup) on eight cell lines (Caco-2, HEK001, MRC-5, HMEC-1, HepaRG, HMC-3, and T47D) at concentrations from 0.01 to 100 μg/mL. Results showed that 100 μg/mL of MPs did not significantly affect cell viability in Caco-2, HEK001, MRC-5, and T47D. However, HMEC-1 and HMC-3 exhibited decreased viability with 10–100 μg/mL of fork particles, while HMC-3 and HepaRG showed reduced viability with 100 μg/mL of cup particles. Conversely, cup particles increased HMEC-1 proliferation at 0.1–100 μg/mL. Comet assay data indicated that both fork and cup exposure led to elevated DNA fragmentation in HMEC-1 and HMC-3 cells. These findings indicate that MPs from consumer-grade plastics may exhibit cytotoxic and genotoxic effects, with endothelial and microglial cells being particularly susceptible.</div></div>\",\"PeriodicalId\":317,\"journal\":{\"name\":\"Food and Chemical Toxicology\",\"volume\":\"196 \",\"pages\":\"Article 115194\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-02-01\",\"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/S0278691524007609\",\"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/S0278691524007609","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

塑料最初是为了保护自然资源而开发的,但由于废物管理不善,塑料已成为一个全球性的污染问题。塑料垃圾在环境中的分散和风化会产生微小的颗粒。尽管对原始聚合物的毒理学效应进行了广泛的研究,但来自消费塑料的微塑料(MPs)的影响却知之甚少。本研究考察了低温加工一次性塑料制品(餐叉和杯)对caco2、HEK001、MRC-5、HMEC-1、HepaRG、HMC-3和T47D等8种细胞系在0.01 ~ 100 μg/mL浓度下的细胞毒性和基因毒性作用。结果显示,100 μg/mL的MPs对Caco-2、HEK001、MRC-5和T47D细胞活力无显著影响。hmc -1和HMC-3在10 ~ 100 μg/mL的叉状颗粒作用下活性降低,而HMC-3和HepaRG在100 μg/mL的杯状颗粒作用下活性降低。相反,杯状颗粒在0.1 ~ 100 μg/mL时可促进HMEC-1的增殖。彗星分析数据表明,叉子和杯子暴露都会导致HMEC-1和HMC-3细胞DNA片段化升高。这些发现表明,来自消费级塑料的MPs可能表现出细胞毒性和基因毒性作用,内皮细胞和小胶质细胞尤其容易受到影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Comparative toxicity of microplastics obtained from human consumer products on human cell-based models
Originally developed to conserve natural resources, plastic has become a global pollution issue due to inadequate waste management. The dispersion and weathering of plastic waste in the environment generate micro-sized particles. Despite extensive research on the toxicological effects of pristine polymers, the impact of microplastics (MPs) from consumer plastics is poorly understood. This study investigated the cytotoxic and genotoxic effects of cryo-milled single-use plastic products (fork and cup) on eight cell lines (Caco-2, HEK001, MRC-5, HMEC-1, HepaRG, HMC-3, and T47D) at concentrations from 0.01 to 100 μg/mL. Results showed that 100 μg/mL of MPs did not significantly affect cell viability in Caco-2, HEK001, MRC-5, and T47D. However, HMEC-1 and HMC-3 exhibited decreased viability with 10–100 μg/mL of fork particles, while HMC-3 and HepaRG showed reduced viability with 100 μg/mL of cup particles. Conversely, cup particles increased HMEC-1 proliferation at 0.1–100 μg/mL. Comet assay data indicated that both fork and cup exposure led to elevated DNA fragmentation in HMEC-1 and HMC-3 cells. These findings indicate that MPs from consumer-grade plastics may exhibit cytotoxic and genotoxic effects, with endothelial and microglial cells being particularly susceptible.
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
Food and Chemical Toxicology
Food and Chemical Toxicology 工程技术-毒理学
CiteScore
10.90
自引率
4.70%
发文量
651
审稿时长
31 days
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.
期刊最新文献
Editorial Board Theaflavin alleviates cisplatin-induced nephrotoxicity: Targeting SIRT1/p53/FOXO3a/Nrf2 signaling and the NF-kB inflammatory cascade Eucalyptol Attenuates Indomethacin-Induced Gastric Ulcers in Rats by Modulating the ICAM-1, eNOS and COX/LOX Pathways: Insights from In Silico, In Vitro and In Vivo Approaches. Acetamiprid-induced pulmonary toxicity via oxidative stress, epithelial-mesenchymal transition, apoptosis, and extracellular matrix accumulation in human lung epithelial cells and fibroblasts: Protective role of heat-killed Lactobacilli. Update to RIFM fragrance ingredient safety assessment, methyl 3,7-dimethyl-6-octenoate, CAS registry number 2270-60-2
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1