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真核细胞中硒氨基酸毒性机制的最新进展。

Recent advances in the mechanism of selenoamino acids toxicity in eukaryotic cells.

作者信息

Lazard Myriam, Dauplais Marc, Blanquet Sylvain, Plateau Pierre

机构信息

.

出版信息

Biomol Concepts. 2017 May 24;8(2):93-104. doi: 10.1515/bmc-2017-0007.

Abstract

Selenium is an essential trace element due to its incorporation into selenoproteins with important biological functions. However, at high doses it is toxic. Selenium toxicity is generally attributed to the induction of oxidative stress. However, it has become apparent that the mode of action of seleno-compounds varies, depending on its chemical form and speciation. Recent studies in various eukaryotic systems, in particular the model organism Saccharomyces cerevisiae, provide new insights on the cytotoxic mechanisms of selenomethionine and selenocysteine. This review first summarizes current knowledge on reactive oxygen species (ROS)-induced genotoxicity of inorganic selenium species. Then, we discuss recent advances on our understanding of the molecular mechanisms of selenocysteine and selenomethionine cytotoxicity. We present evidences indicating that both oxidative stress and ROS-independent mechanisms contribute to selenoamino acids cytotoxicity. These latter mechanisms include disruption of protein homeostasis by selenocysteine misincorporation in proteins and/or reaction of selenols with protein thiols.

摘要

硒是一种必需的微量元素,因为它会被整合到具有重要生物学功能的硒蛋白中。然而,高剂量时它是有毒的。硒中毒通常归因于氧化应激的诱导。然而,很明显,硒化合物的作用方式因其化学形式和形态而异。最近在各种真核系统中的研究,特别是模式生物酿酒酵母,为硒代蛋氨酸和硒代半胱氨酸的细胞毒性机制提供了新的见解。本综述首先总结了关于活性氧(ROS)诱导的无机硒物种遗传毒性的现有知识。然后,我们讨论了我们对硒代半胱氨酸和硒代蛋氨酸细胞毒性分子机制理解的最新进展。我们提供的证据表明,氧化应激和不依赖ROS的机制都导致了硒代氨基酸的细胞毒性。后一种机制包括通过硒代半胱氨酸错误掺入蛋白质而破坏蛋白质稳态和/或硒醇与蛋白质硫醇的反应。

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