Blum Jonathan, Masjosthusmann Stefan, Bartmann Kristina, Bendt Farina, Dolde Xenia, Dönmez Arif, Förster Nils, Holzer Anna-Katharina, Hübenthal Ulrike, Keßel Hagen Eike, Kilic Sadiye, Klose Jördis, Pahl Melanie, Stürzl Lynn-Christin, Mangas Iris, Terron Andrea, Crofton Kevin M, Scholze Martin, Mosig Axel, Leist Marcel, Fritsche Ellen
In Vitro Toxicology and Biomedicine, Dept Inaugurated By the Doerenkamp-Zbinden Foundation, University of Konstanz, 78457, Konstanz, Germany.
IUF - Leibniz Research Institute for Environmental Medicine, 40225, Düsseldorf, Germany.
Chemosphere. 2023 Jan;311(Pt 2):137035. doi: 10.1016/j.chemosphere.2022.137035. Epub 2022 Oct 31.
Developmental neurotoxicity (DNT) is a major safety concern for all chemicals of the human exposome. However, DNT data from animal studies are available for only a small percentage of manufactured compounds. Test methods with a higher throughput than current regulatory guideline methods, and with improved human relevance are urgently needed. We therefore explored the feasibility of DNT hazard assessment based on new approach methods (NAMs). An in vitro battery (IVB) was assembled from ten individual NAMs that had been developed during the past years to probe effects of chemicals on various fundamental neurodevelopmental processes. All assays used human neural cells at different developmental stages. This allowed us to assess disturbances of: (i) proliferation of neural progenitor cells (NPC); (ii) migration of neural crest cells, radial glia cells, neurons and oligodendrocytes; (iii) differentiation of NPC into neurons and oligodendrocytes; and (iv) neurite outgrowth of peripheral and central neurons. In parallel, cytotoxicity measures were obtained. The feasibility of concentration-dependent screening and of a reliable biostatistical processing of the complex multi-dimensional data was explored with a set of 120 test compounds, containing subsets of pre-defined positive and negative DNT compounds. The battery provided alerts (hit or borderline) for 24 of 28 known toxicants (82% sensitivity), and for none of the 17 negative controls. Based on the results from this screen project, strategies were developed on how IVB data may be used in the context of risk assessment scenarios employing integrated approaches for testing and assessment (IATA).
发育神经毒性(DNT)是人类暴露组中所有化学物质的主要安全问题。然而,动物研究中的DNT数据仅适用于一小部分人造化合物。迫切需要比当前监管指南方法通量更高且与人类相关性更强的测试方法。因此,我们探索了基于新方法(NAMs)进行DNT危害评估的可行性。一个体外试验组合(IVB)由过去几年开发的十种单独的NAMs组成,用于探究化学物质对各种基本神经发育过程的影响。所有试验均使用不同发育阶段的人类神经细胞。这使我们能够评估以下方面的干扰:(i)神经祖细胞(NPC)的增殖;(ii)神经嵴细胞、放射状胶质细胞、神经元和少突胶质细胞的迁移;(iii)NPC向神经元和少突胶质细胞的分化;以及(iv)外周和中枢神经元的神经突生长。同时,获得了细胞毒性测量结果。使用一组120种测试化合物(包括预定义的阳性和阴性DNT化合物子集)探索了浓度依赖性筛选以及对复杂多维数据进行可靠生物统计学处理的可行性。该试验组合对28种已知毒物中的24种发出了警报(命中或临界)(敏感性为82%),而对17个阴性对照均未发出警报。基于该筛选项目的结果,制定了关于如何在采用综合测试与评估方法(IATA)的风险评估场景中使用IVB数据的策略。