Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; The Institute for Environmental Health Solutions, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Curriculum in Toxicology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Toxicol Appl Pharmacol. 2019 Sep 1;378:114635. doi: 10.1016/j.taap.2019.114635. Epub 2019 Jun 22.
During pregnancy, the placenta is critical for the regulation of maternal homeostasis and fetal growth and development. Exposures to environmental chemicals during pregnancy can be detrimental to the health of the placenta and therefore adversely impact maternal and fetal health. Though research on placental-derived developmental toxicity is expanding, testing is limited by the resources required for traditional test methods based on whole animal experimentation. Alternative strategies utilizing in vitro methods are well suited to contribute to more efficient screening of chemical toxicity and identification of biological mechanisms underlying toxicity outcomes. This review aims to summarize methods that can be used to evaluate toxicity resulting from exposures during the prenatal period, with a focus on newer in vitro methods centered on placental toxicity. The following key aspects are reviewed: (i) traditional test methods based on animal developmental toxicity testing, (ii) in vitro methods using monocultures and explant models, as well as more recently developed methods, including co-cultures, placenta-on-a-chip, and 3-dimensional (3D) cell models, (iii) endpoints that are commonly measured using in vitro designs, and (iv) the translation of in vitro methods into chemical evaluations and risk assessment applications. We conclude that findings from in vitro placental models can contribute to the screening of potentially hazardous chemicals, elucidation of chemical mechanism of action, incorporation into adverse outcome pathways, estimation of doses eliciting toxicity, derivation of extrapolation factors, and characterization of overall risk of adverse outcomes, representing key components of chemical regulation in the 21 century.
在妊娠期间,胎盘对于母体的内环境稳定和胎儿的生长发育至关重要。妊娠期间暴露于环境化学物质可能会对胎盘健康造成损害,从而对母婴健康产生不利影响。尽管关于胎盘来源的发育毒性的研究正在不断扩展,但由于基于动物实验的传统测试方法需要大量资源,因此测试受到限制。利用体外方法的替代策略非常适合更有效地筛选化学毒性并确定毒性结果的生物学机制。本文旨在总结可用于评估产前暴露引起的毒性的方法,重点介绍新的以胎盘毒性为中心的体外方法。本文回顾了以下关键方面:(i)基于动物发育毒性测试的传统测试方法,(ii)使用单核细胞培养物和器官培养模型的体外方法,以及最近开发的方法,包括共培养、胎盘芯片和 3 维(3D)细胞模型,(iii)使用体外设计常用的终点,以及(iv)将体外方法转化为化学评估和风险评估应用。我们得出结论,体外胎盘模型的研究结果可以为潜在有害化学物质的筛选、化学作用机制的阐明、不良结局途径的纳入、引起毒性的剂量估计、外推因子的推导以及不良结局的总体风险特征提供信息,这些都是 21 世纪化学监管的关键组成部分。