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金属硫蛋白的合成与降解:与镉代谢的关系。

Metallothionein synthesis and degradation: relationship to cadmium metabolism.

作者信息

Cousins R J

出版信息

Environ Health Perspect. 1979 Feb;28:131-6. doi: 10.1289/ehp.7928131.

Abstract

Metallothionein is an integral component of the mechanism that regulates the metabolism of cadmium and zinc. The synthesis of this protein can be "induced" by oral or parenteral administration of either metal. The metallothionein mRNA content of liver polysomes is increased shortly after an influx of small amounts of either metal into hepatocytes. After sufficient amounts of this poly (A+) RNA have been synthesized, there is a concomitant increase in metallothionein biosynthesis and metal binding. Unlike synthesis, the degradation of metallothionein is markedly influenced by the species of metal bound. By using in vivo and in vitro techniques, it has been possible to demonstrate that resistance of metallothionein to degradation follows the order: thionein less than zinc metallothionein less than cadmium metallothionein. Moreover, while the polypeptide chains of cadmium metallothionein are degraded, it appears that liberated cadmium ions are quickly incorporated into nascent chains of thionein. The latter explains why the cadmium content of liver and kidney increases with age and environmental exposure. Since both zinc and cadmium bind to metallothionein, it appears that the binding sites provided by this inducible species provide a locus for interaction between zinc, a nutrient, and cadmium, an environmental contaminant.

摘要

金属硫蛋白是调节镉和锌代谢机制的一个不可或缺的组成部分。口服或肠胃外给予这两种金属中的任何一种都能“诱导”这种蛋白质的合成。少量的任何一种金属流入肝细胞后不久,肝多核糖体中的金属硫蛋白mRNA含量就会增加。在合成了足够量的这种聚腺苷酸(A+)RNA后,金属硫蛋白的生物合成和金属结合会随之增加。与合成不同,金属硫蛋白的降解受到所结合金属种类的显著影响。通过使用体内和体外技术,已经能够证明金属硫蛋白对降解的抗性顺序为:硫蛋白<锌金属硫蛋白<镉金属硫蛋白。此外,虽然镉金属硫蛋白的多肽链会降解,但释放出的镉离子似乎会迅速掺入硫蛋白的新生链中。后者解释了肝脏和肾脏中的镉含量为何会随着年龄增长和环境暴露而增加。由于锌和镉都与金属硫蛋白结合,这种可诱导物质提供的结合位点似乎为营养素锌和环境污染物镉之间的相互作用提供了一个场所。

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