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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生物和人群健康联系起来:线粒体不良结果途径的进展和考虑

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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主要目标,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。这些直接相互作用充当分子引发事件,阻碍了三磷酸腺苷的产生和线粒体在细胞内发挥作用的其他关键功能(例如钙和金属稳态,细胞凋亡,免疫信号传导,氧化还原平衡)。已经提出了数量有限但数量不断增加的不良结局途径(AOP),以将线粒体功能障碍与机体和人群水平的影响联系起来。这些途径涉及关键事件,例如膜电位改变,线粒体裂变/融合和线粒体DNA损伤等。本批判性审查和分析揭示了涉及线粒体功能障碍的AOPs的最新进展,并使用基于网络的计算方法确定了多个现有AOPs中线粒体分子引发事件和关键事件的定位。我们还提供了2个案例研究,第一个研究线粒体与免疫毒性之间的相互作用,第二个研究早期线粒体功能障碍在行为(即运动活动)方面的作用。我们在目前对线粒体AOP的理解中讨论局限性,并着重阐明其细节的机会。要提高我们在AOP框架内对关键事件关系的了解,将需要高通量的数据集,以允许开发和测试与化学无关的AOP,以及进行高分辨率研究,以增强这些关键事件关系的机械测试和验证。考虑到影响线粒体的化学物质种类繁多,并且能量产生和对重要生态结果(例如病原体防御,体内稳态,生长和繁殖)的信号传递具有中心作用,因此,对线粒体AOP的更好理解(即使不是中心作用)也有望发挥重要作用,在环境毒理学中的作用。 Environ Toxicol Chem 2019; 38:1625-1634。 (c)2019年SETAC

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