Moore Michael N, Kohler Angela, Lowe David, Viarengo Aldo
Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, United Kingdom.
Methods Enzymol. 2008;451:581-620. doi: 10.1016/S0076-6879(08)03233-3.
The lysosomal-autophagic system appears to be a common target for many environmental pollutants, as lysosomes accumulate many toxic metals and organic xenobiotics, which perturb normal function and damage the lysosomal membrane. In fact, autophagic reactions frequently involving reduced lysosomal membrane integrity or stability appear to be effective generic indicators of cellular well-being in eukaryotes: in social amoebae (slime mold), mollusks and fish, autophagy/membrane destabilization is correlated with many stress and toxicological responses and pathological reactions. Prognostic use of adverse lysosomal and autophagic reactions to environmental pollutants can be used for predicting cellular dysfunction and health in aquatic animals, such as shellfish and fish, which are extensively used as sensitive bioindicators in monitoring ecosystem health; and also represent a significant food resource for at least 20% of the global human population. Explanatory frameworks for prediction of pollutant impact on health have been derived encompassing a conceptual mechanistic model linking lysosomal damage and autophagic dysfunction with injury to cells and tissues. Methods are described for tracking in vivo autophagy of fluorescently labeled cytoplasmic proteins, measuring degradation of radiolabeled intracellular proteins and morphometric measurement of lysosomal/cytoplasmic volume ratio. Additional methods for the determination of lysosomal membrane stability in lower animals are also described, which can be applied to frozen tissue sections, protozoans and isolated cells in vivo. Experimental and simulated results have also indicated that nutritional deprivation (analogous in marine mussels to caloric restriction)-induced autophagy has a protective function against toxic effects mediated by reactive oxygen species (ROS). Finally, coupled measurement of lysosomal-autophagic reactions and simulation modelling is proposed as a practical toolbox for predicting toxic environmental risk.
溶酶体自噬系统似乎是许多环境污染物的共同靶点,因为溶酶体积累了许多有毒金属和有机外源性物质,这些物质会扰乱正常功能并损害溶酶体膜。事实上,频繁涉及溶酶体膜完整性或稳定性降低的自噬反应似乎是真核生物细胞健康的有效通用指标:在社会性变形虫(黏菌)、软体动物和鱼类中,自噬/膜去稳定化与许多应激、毒理学反应和病理反应相关。对环境污染物产生的不良溶酶体和自噬反应进行预后评估,可用于预测水生动物(如贝类和鱼类)的细胞功能障碍和健康状况,这些动物在监测生态系统健康方面被广泛用作敏感的生物指标;并且至少为全球20%的人口提供了重要的食物资源。已经得出了预测污染物对健康影响的解释框架,其中包括一个将溶酶体损伤和自噬功能障碍与细胞和组织损伤联系起来的概念性机制模型。描述了跟踪荧光标记细胞质蛋白体内自噬、测量放射性标记细胞内蛋白降解以及溶酶体/细胞质体积比形态计量学测量的方法。还描述了测定低等动物溶酶体膜稳定性的其他方法,这些方法可应用于冷冻组织切片、原生动物和体内分离细胞。实验和模拟结果还表明,营养剥夺(在海洋贻贝中类似于热量限制)诱导的自噬对活性氧(ROS)介导的毒性作用具有保护功能。最后,提出将溶酶体自噬反应的耦合测量和模拟建模作为预测有毒环境风险的实用工具箱。