Selenium and GPX4, a vital symbiosis

被引:149
作者
Angeli, Jose Pedro Friedmann [1 ]
Conrad, Marcus [2 ]
机构
[1] Univ Wurzburg, Rudolf Virchow Ctr Expt Biomed, D-97080 Wurzburg, Germany
[2] Helmholtz Zentrum Munchen, Inst Dev Genet, D-85764 Neuherberg, Germany
关键词
Cell death; Cholesterol metabolism; Embryogenesis; Ferroptosis; Selenoproteins; GLUTATHIONE-PEROXIDASE; 4; TRANSFER-RNA GENE; PROGRESSIVE CEREBELLOCEREBRAL ATROPHY; MITOCHONDRIAL THIOREDOXIN REDUCTASE; SELENOPROTEIN EXPRESSION; TARGETED DISRUPTION; SELENOCYSTEINE INSERTION; CELL-DEATH; MOUSE; FERROPTOSIS;
D O I
10.1016/j.freeradbiomed.2018.03.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Selenium has transitioned from an environmental poison and carcinogen to an essential micronutrient associated with a broad array of health promoting effects. These beneficial effects are now accepted to be linked to its incorporation into selenoproteins, a family of rare proteins utilizing a specialized translation machinery to integrate selenium in the form of selenocysteine. Despite this recognized role, much less is known regarding the actual role of selenium in these proteins. Here, we will provide the reader with an overview of the essential role of specific selenoproteins and their link to pathology based on mouse studies and relevant mutations discovered in humans. Additionally, we will cover recent insights linking a non-interchangeable role for selenium in glutathione peroxidase 4 and its function in suppressing ferroptosis. This critical dependency ultimately generates a strong reliance on metabolic pathways that regulate selenium metabolism and its incorporation into proteins, such as the mevalonate pathway.
引用
收藏
页码:153 / 159
页数:7
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