Mirjana Nacka-Aleksić , Aleksandra Vilotić , Andrea Pirković , Marko Živanović , Biljana Ljujić , Milica Jovanović Krivokuća
{"title":"Nano-scale dangers: Unravelling the impact of nanoplastics on human trophoblast invasion","authors":"Mirjana Nacka-Aleksić , Aleksandra Vilotić , Andrea Pirković , Marko Živanović , Biljana Ljujić , Milica Jovanović Krivokuća","doi":"10.1016/j.cbi.2024.111317","DOIUrl":null,"url":null,"abstract":"<div><div>Utilizing HTR-8/SVneo cells for <em>in vitro</em> modeling of human trophoblast invasion, we examined how different concentrations of 40 nm and 200 nm carboxylated polystyrene particles affect early-pregnancy trophoblast phenotype and function. We focused on migration and invasion, as critical processes in placental development. Our findings revealed disruptions in extravillous trophoblast mesenchymal phenotype and invasive behavior, following acute exposure to a higher concentration of the smaller sized particles. Specifically, differential uptake of the particles by trophoblast cells was observed, as well as cytotoxicity and concentration-dependent DNA damage after 72 h of exposure. In addition, a 24 h exposure to 100 μg/ml of 40 nm particles correlated with downregulated protein expression of α5 and α1 integrin subunits, N-cadherin, matrix metalloproteinase-2 and macrophage migration inhibitory factor, alongside upregulated protein expression of the epithelial marker E-cadherin. These changes likely contributed to the diminished migration of HTR-8/SVneo cells and the invasive potential of HTR-8/SVneo spheroids. Understanding these interactions is paramount for assessing the broader implications of nanoplastics on reproductive outcomes and maternal-fetal well-being and informing public health measures.</div></div>","PeriodicalId":274,"journal":{"name":"Chemico-Biological Interactions","volume":"405 ","pages":"Article 111317"},"PeriodicalIF":4.7000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemico-Biological Interactions","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009279724004630","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Utilizing HTR-8/SVneo cells for in vitro modeling of human trophoblast invasion, we examined how different concentrations of 40 nm and 200 nm carboxylated polystyrene particles affect early-pregnancy trophoblast phenotype and function. We focused on migration and invasion, as critical processes in placental development. Our findings revealed disruptions in extravillous trophoblast mesenchymal phenotype and invasive behavior, following acute exposure to a higher concentration of the smaller sized particles. Specifically, differential uptake of the particles by trophoblast cells was observed, as well as cytotoxicity and concentration-dependent DNA damage after 72 h of exposure. In addition, a 24 h exposure to 100 μg/ml of 40 nm particles correlated with downregulated protein expression of α5 and α1 integrin subunits, N-cadherin, matrix metalloproteinase-2 and macrophage migration inhibitory factor, alongside upregulated protein expression of the epithelial marker E-cadherin. These changes likely contributed to the diminished migration of HTR-8/SVneo cells and the invasive potential of HTR-8/SVneo spheroids. Understanding these interactions is paramount for assessing the broader implications of nanoplastics on reproductive outcomes and maternal-fetal well-being and informing public health measures.
期刊介绍:
Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.