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小鼠肝脏中管家硒蛋白表达的缺失调节脂蛋白代谢。

Loss of housekeeping selenoprotein expression in mouse liver modulates lipoprotein metabolism.

作者信息

Sengupta Aniruddha, Carlson Bradley A, Hoffmann Victoria J, Gladyshev Vadim N, Hatfield Dolph L

机构信息

Molecular Biology of Selenium Section, Laboratory of Cancer Prevention, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Biochem Biophys Res Commun. 2008 Jan 18;365(3):446-52. doi: 10.1016/j.bbrc.2007.10.189. Epub 2007 Nov 9.

Abstract

Selenium is incorporated into proteins as selenocysteine (Sec), which is dependent on its specific tRNA, designated tRNA([Ser]Sec). Targeted removal of the tRNA([Ser]Sec) gene (Trsp) in mouse hepatocytes previously demonstrated the importance of selenoproteins in liver function. Herein, analysis of plasma proteins in this Trsp knockout mouse revealed increases in apolipoprotein E (ApoE) that was accompanied by elevated plasma cholesterol levels. The expression of genes involved in cholesterol biosynthesis, metabolism and transport were also altered in knockout mice. Additionally, in two transgenic Trsp mutant mouse lines (wherein only housekeeping selenoprotein synthesis was restored), the expression of ApoE, as well as genes involved in cholesterol biosynthesis, metabolism and transport were similar to those observed in wild type mice. These data correlate with reports that selenium deficiency results in increased levels of ApoE, indicating for the first time that housekeeping selenoproteins have a role in regulating lipoprotein biosynthesis and metabolism.

摘要

硒作为硒代半胱氨酸(Sec)掺入蛋白质中,这依赖于其特定的tRNA,即tRNA([Ser]Sec)。先前在小鼠肝细胞中靶向去除tRNA([Ser]Sec)基因(Trsp)证明了硒蛋白在肝功能中的重要性。在此,对这种Trsp基因敲除小鼠的血浆蛋白分析显示载脂蛋白E(ApoE)增加,同时血浆胆固醇水平升高。参与胆固醇生物合成、代谢和转运的基因表达在基因敲除小鼠中也发生了改变。此外,在两个转基因Trsp突变小鼠品系中(其中仅恢复了管家硒蛋白的合成),ApoE以及参与胆固醇生物合成、代谢和转运的基因表达与野生型小鼠中观察到的相似。这些数据与硒缺乏导致ApoE水平升高的报道相关,首次表明管家硒蛋白在调节脂蛋白生物合成和代谢中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cd/2175387/e71453517a81/nihms36097f1.jpg

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