Nanoplastic at environmentally relevant concentrations activates germline mir-240-rab-5 signaling cascade to affect secreted ligands associated with transgenerational toxicity induction in C. elegans

IF 5.8 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Environmental Science: Nano Pub Date : 2024-07-02 DOI:10.1039/d4en00309h
Xin Hua, Le Zhang, Dayong Wang
{"title":"Nanoplastic at environmentally relevant concentrations activates germline mir-240-rab-5 signaling cascade to affect secreted ligands associated with transgenerational toxicity induction in C. elegans","authors":"Xin Hua, Le Zhang, Dayong Wang","doi":"10.1039/d4en00309h","DOIUrl":null,"url":null,"abstract":"Epigenetic regulation plays an important role in regulating the transgenerational toxicity of pollutants. However, underlying mechanism of microRNAs (miRNAs) in regulating transgenerational nanoplastic toxicity remains largely unclear. We aimed to determine miRNA-mediated mechanism for induction of transgenerational nanoplastic toxicity. In Caenorhabditis elegans, although germline RNAi of both mir-240 and mir-36 suppressed polystyrene nanoparticle (PS-NP) toxicity, exposure to PS-NP (1-100 μg/L) only increased mir-240 expression. Transgenerational increase in mir-240 expression was observed after PS-NP exposure at P0 generation (P0-G), and germline RNAi of mir-240 suppressed transgenerational PS-NP toxicity. Among predicted target genes of mir-240 in the germline, exposure to PS-NP (1-100 μg/L) decreased rab-5 and rab-6.2 expressions, whereas germline RNAi of mir-240 only increased rab-5 expression in PS-NP exposed nematodes. Transgenerational decrease in rab-5 expression was detected after PS-NP exposure at P0-G, and germline RNAi of rab-5 strengthened transgenerational PS-NP toxicity. Moreover, the resistance of mir-240(RNAi) to transgenerational PS-NP toxicity in inhibiting locomotion behavior and in reducing brood size was inhibited by germline RNAi of rab-5. Among secreted ligands, germline RNAi of rab-5 increased expressions of genes encoding insulin peptides (ins-3, ins-39, and daf-28), FGF ligand (egl-17), and Ephrin ligand (efn-3) in PS-NP exposed nematodes and their corresponding receptor genes (daf-2, egl-15, and vab-1) in offspring of PS-NP exposed nematodes. Therefore, increase in germline mir-240 mediated transgenerational PS-NP toxicity through insulin, FGF, and Ephrin signals by affecting its target of RAB-5. Our data provided important involvement of germline microRNA in mediating nanoplastic toxicity across multiple generations in organisms.","PeriodicalId":73,"journal":{"name":"Environmental Science: Nano","volume":null,"pages":null},"PeriodicalIF":5.8000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science: Nano","FirstCategoryId":"6","ListUrlMain":"https://doi.org/10.1039/d4en00309h","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Epigenetic regulation plays an important role in regulating the transgenerational toxicity of pollutants. However, underlying mechanism of microRNAs (miRNAs) in regulating transgenerational nanoplastic toxicity remains largely unclear. We aimed to determine miRNA-mediated mechanism for induction of transgenerational nanoplastic toxicity. In Caenorhabditis elegans, although germline RNAi of both mir-240 and mir-36 suppressed polystyrene nanoparticle (PS-NP) toxicity, exposure to PS-NP (1-100 μg/L) only increased mir-240 expression. Transgenerational increase in mir-240 expression was observed after PS-NP exposure at P0 generation (P0-G), and germline RNAi of mir-240 suppressed transgenerational PS-NP toxicity. Among predicted target genes of mir-240 in the germline, exposure to PS-NP (1-100 μg/L) decreased rab-5 and rab-6.2 expressions, whereas germline RNAi of mir-240 only increased rab-5 expression in PS-NP exposed nematodes. Transgenerational decrease in rab-5 expression was detected after PS-NP exposure at P0-G, and germline RNAi of rab-5 strengthened transgenerational PS-NP toxicity. Moreover, the resistance of mir-240(RNAi) to transgenerational PS-NP toxicity in inhibiting locomotion behavior and in reducing brood size was inhibited by germline RNAi of rab-5. Among secreted ligands, germline RNAi of rab-5 increased expressions of genes encoding insulin peptides (ins-3, ins-39, and daf-28), FGF ligand (egl-17), and Ephrin ligand (efn-3) in PS-NP exposed nematodes and their corresponding receptor genes (daf-2, egl-15, and vab-1) in offspring of PS-NP exposed nematodes. Therefore, increase in germline mir-240 mediated transgenerational PS-NP toxicity through insulin, FGF, and Ephrin signals by affecting its target of RAB-5. Our data provided important involvement of germline microRNA in mediating nanoplastic toxicity across multiple generations in organisms.
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
环境相关浓度的纳米塑料可激活种系 mir-240-rab-5 信号级联,从而影响与秀丽隐杆线虫转代毒性诱导相关的分泌配体
表观遗传调控在调节污染物的跨代毒性方面发挥着重要作用。然而,microRNAs(miRNAs)调控纳米塑料跨代毒性的内在机制在很大程度上仍不清楚。我们旨在确定 miRNA 介导的纳米塑料跨代毒性诱导机制。在秀丽隐杆线虫(Caenorhabditis elegans)中,虽然mir-240和mir-36的种系RNAi抑制了聚苯乙烯纳米粒子(PS-NP)的毒性,但暴露于PS-NP(1-100 μg/L)仅增加了mir-240的表达。在P0代(P0-G)暴露于PS-NP后,可观察到mir-240表达的跨代增加,mir-240的种系RNAi抑制了PS-NP的跨代毒性。在种系mir-240的预测靶基因中,暴露于PS-NP(1-100 μg/L)会降低rab-5和rab-6.2的表达,而在暴露于PS-NP的线虫中,mir-240的种系RNAi只会增加rab-5的表达。在P0-G暴露于PS-NP后,发现rab-5表达量会出现代际下降,而rab-5的种系RNAi会加强PS-NP的代际毒性。此外,rab-5的种系RNAi抑制了mir-240(RNAi)对转代PS-NP毒性的抗性,即抑制运动行为和减少育雏规模。在分泌配体中,rab-5的种系RNAi增加了暴露于PS-NP的线虫体内编码胰岛素肽(ins-3、ins-39和daf-28)、FGF配体(egl-17)和Ephrin配体(efn-3)的基因的表达,也增加了暴露于PS-NP的线虫后代体内其相应受体基因(daf-2、egl-15和vab-1)的表达。因此,种系mir-240的增加通过影响其靶标RAB-5,通过胰岛素、FGF和Ephrin信号介导了转代PS-NP毒性。我们的数据提供了种系microRNA在介导生物多代纳米塑料毒性中的重要参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Environmental Science: Nano
Environmental Science: Nano CHEMISTRY, MULTIDISCIPLINARY-ENVIRONMENTAL SCIENCES
CiteScore
12.20
自引率
5.50%
发文量
290
审稿时长
2.1 months
期刊介绍: Environmental Science: Nano serves as a comprehensive and high-impact peer-reviewed source of information on the design and demonstration of engineered nanomaterials for environment-based applications. It also covers the interactions between engineered, natural, and incidental nanomaterials with biological and environmental systems. This scope includes, but is not limited to, the following topic areas: Novel nanomaterial-based applications for water, air, soil, food, and energy sustainability Nanomaterial interactions with biological systems and nanotoxicology Environmental fate, reactivity, and transformations of nanoscale materials Nanoscale processes in the environment Sustainable nanotechnology including rational nanomaterial design, life cycle assessment, risk/benefit analysis
期刊最新文献
Correction: Harnessing nanobiotechnology for drought stress: transforming agriculture's future; what, why and how? Investigating the vital influences of multi-factor synergies on the nitrate formations on the surface of nano MgO particles A superhydrophobic nanocrystalline MOF embedded starch@cotton composite for fast, selective and nanomolar sensing and adsorptive removal of a fluorinated herbicide from aqueous medium Morphologic alterations across three levels of biological organization following oral exposure to silver-polymer nanocomposites in Japanese medaka (Oryzias latipes) Degradation and detection of tetracycline by a bifunctional Bi4Ti3O12/Ag heterojunction under light and piezoelectric effect
×
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
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