a School of Environmental Engineering , University of Seoul , Seoul , Korea.
b Department of Life Science , University of Seoul , Seoul , Korea.
Nanotoxicology. 2018 Dec;12(10):1182-1197. doi: 10.1080/17435390.2018.1529835. Epub 2019 Jan 21.
An adverse outcome pathway (AOP) is a framework that organizes the mechanistic or predictive relationships between molecular initiating events (MIEs), key events (KEs), and adverse outcomes (AOs). Previously, we intensively investigated the molecular mechanism that underlies toxicity caused by AgNPs in the nematode Caenorhabditis elegans. Using transcriptomics, functional genetics, and various molecular/biochemical tools, we identified oxidative stress as the major mechanism underlying toxicity and reproduction failure as the outcome. With this information, here we conducted a case study of building an AOP to link oxidative stress with reproductive toxicity. To validate this AOP, we filled the gaps by conducting further experiments on its elements, such as NADPH oxidase, ROS formation, PMK-1 P38 MAPK activation, HIF-1 activation, mitochondrial damage, DNA damage, and apoptosis. The establishment of a causal link between the MIE and AO is critical for the construction of an AOP. Therefore, causal relationships between each KE and AO were verified by using functional genetic mutants of each KE. By combining these experimental data with our previously published results, we established causal relationships between the MIE, KEs, and AO using a Bayesian network (BN) model, culminating in an AOP entitled 'NADPH oxidase and P38 MAPK activation leading to reproductive failure in C. elegans ( https://aopwiki.org/aops/207)' . Overall, our approach shows that an AOP can be developed using existing data and further experiments can be conducted to fill the gaps between the MIE, KEs, and the AO. This study also shows that BN modeling has the potential to identify causal relationships in an AOP.
一种不良结局途径 (AOP) 是一种框架,用于组织分子起始事件 (MIE)、关键事件 (KE) 和不良结局 (AO) 之间的机制或预测关系。之前,我们深入研究了纳米银颗粒在秀丽隐杆线虫中引起毒性的分子机制。使用转录组学、功能遗传学和各种分子/生化工具,我们确定氧化应激是毒性和生殖失败的主要机制,生殖失败是其结局。有了这些信息,我们在这里进行了构建 AOP 将氧化应激与生殖毒性联系起来的案例研究。为了验证这个 AOP,我们通过对其元素(如 NADPH 氧化酶、ROS 形成、PMK-1 P38 MAPK 激活、HIF-1 激活、线粒体损伤、DNA 损伤和细胞凋亡)进行进一步的实验来填补空白。建立 MIE 和 AO 之间的因果关系对于构建 AOP 至关重要。因此,通过使用每个 KE 的功能遗传突变体,验证了每个 KE 和 AO 之间的因果关系。通过将这些实验数据与我们之前发表的结果相结合,我们使用贝叶斯网络 (BN) 模型建立了 MIE、KE 和 AO 之间的因果关系,最终形成了一个题为“NADPH 氧化酶和 P38 MAPK 激活导致秀丽隐杆线虫生殖失败”的 AOP(https://aopwiki.org/aops/207)。总的来说,我们的方法表明,可以使用现有数据来开发 AOP,并且可以进行进一步的实验来填补 MIE、KE 和 AO 之间的空白。这项研究还表明,BN 建模有可能识别 AOP 中的因果关系。