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首页> 外文期刊>Environmental toxicology and chemistry >Linking Mitochondrial Dysfunction to Organismal and Population Health in the Context of Environmental Pollutants:Progress and Considerations for Mitochondrial Adverse Outcome Pathways
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Linking Mitochondrial Dysfunction to Organismal and Population Health in the Context of Environmental Pollutants:Progress and Considerations for Mitochondrial Adverse Outcome Pathways

机译:在环境污染物的背景下将线粒体功能障碍与有机体和人口健康联系起来:线粒体不良结果途径的进展和考虑因素

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Mitochondria are key targets of many environmental contaminants, because specific chemicals can interact directly with mitochondrial proteins, lipids, and ribonucleic acids. These direct interactions serve as molecular initiating events that impede adenosine triphosphate production and other critical functions that mitochondria serve within the cell (e.g., calcium and metal homeostasis, apoptosis, immune signaling, redox balance). A limited but growing number of adverse outcome pathways (AOPs) have been proposed to associate mitochondrial dysfunction with effects at organismal and population levels. These pathways involve key events such as altered membrane potential, mitochondrial fission/fusion, and mitochondrial DNA damage, among others. The present critical review and analysis reveals current progress on AOPs involving mitochondrial dysfunction, and, using a network-based computational approach, identifies the localization of mitochondrial molecular initiating events and key events within multiple existing AOPs. We also present 2 case studies, the first examining the interaction between mitochondria and immunotoxicity, and the second examining the role of early mitochondrial dysfunction in the context of behavior (i.e., locomotor activity). We discuss limitations in our current understanding of mitochondrial AOPs and highlight opportunities for clarifying their details. Advancing our knowledge of key event relationships within the AOP framework will require high-throughput datasets that permit the development and testing of chemical-agnostic AOPs, as well as high-resolution research that will enhance the mechanistic testing and validation of these key event relationships. Given the wide range of chemicals that affect mitochondria, and the centrality of energy production and signaling to ecologically important outcomes such as pathogen defense, homeostasis, growth, and reproduction, a better understanding of mitochondrial AOPs is expected to play a significant, if not central, role in environmental toxicology. Environ Toxicol Chem 2019;38:1625-1634. (c) 2019 SETAC
机译:线粒体是许多环境污染物的关键目标,因为特定的化学物质可以直接与线粒体蛋白,脂质和核糖核酸相互作用。这些直接相互作用用作分子启动事件,该事件妨碍三磷酸盐的生产和线粒体在细胞内存在细胞内的其他关键功能(例如,钙和金属稳态,细胞凋亡,免疫信号,氧化还原平衡)。已经提出了有限但越来越多的不利结果途径(AOP),以将线粒体功能障碍与有机体和人口水平的效果联系起来。这些途径涉及关键事件,例如改变的膜电位,线粒体裂变/融合和线粒体DNA损伤等。目前的审查和分析揭示了涉及线粒体功能障碍的AOP的当前进展,并且使用基于网络的计算方法,识别线粒体分子发起事件的定位和多个现有AOP内的关键事件。我们还提出了2个案例研究,第一次检查线粒体和免疫毒性之间的相互作用,以及第二次检查早期线粒体功能障碍在行为背景下的作用(即运动活动)。我们讨论了我们目前对线粒体AOP的理解,并突出了澄清他们的细节的机会。推进我们对AOP框架内的关键事件关系的了解,将需要高吞吐量数据集,允许对化学无关的AOP的开发和测试以及高分辨率研究,以提高这些关键事件关系的机制测试和验证。鉴于影响线粒体的广泛化学品,以及能源生产和信号传导至生态上重要成果,如病原体防御,稳态,生长和繁殖,预计会更好地了解线粒体AOP,如果不是中央,则会发挥重要意义,在环境毒理学中的作用。环境毒素科学2019; 38:1625-1634。 (c)2019 Setac

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