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首页> 外文期刊>The biochemical journal >Expression of phosphatidylethanolamine N-methyltransferase-2 in McArdle-RH7777 hepatoma cells inhibits the CDP-choline pathway for phosphatidylcholine biosynthesis via decreased gene expression of CTP:phosphocholine cytidylyltransferase
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Expression of phosphatidylethanolamine N-methyltransferase-2 in McArdle-RH7777 hepatoma cells inhibits the CDP-choline pathway for phosphatidylcholine biosynthesis via decreased gene expression of CTP:phosphocholine cytidylyltransferase

机译:McArdle-RH7777肝癌细胞中磷脂酰乙醇胺N-甲基转移酶2的表达通过降低CTP:磷脂酰胆碱基转移酶的基因表达来抑制CDP-胆碱途径的磷脂酰胆碱生物合成。

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pPhosphatidylethanolamine N-methyltransferase-2 (PEMT2) of rat liver was expressed in McArdle-RH7777 rat hepatoma cells, which lack endogenous PEMT activity. Expression of the enzyme was confirmed by assay of PEMT activity and immunoblotting. There was no change in the amount of phosphatidylcholine in the transfected cells [Cu, Houweling and Vance (1994) J. Biol. Chem. 269, 24531-24533], even though the expression of PEMT2 caused an increased incorporation of [methyl-3H]methionine and [3H]ethanolamine into phosphatidylcholine. In contrast, [3H]serine incorporation into phosphatidylcholine was only marginally enhanced by PEMT2 expression. Incorporation of [methyl-3H]choline into phosphatidylcholine was decreased by greater than 60%, suggesting that the CDP-choline pathway was inhibited as a result of PEMT2 expression. CTP:phosphocholine cytidylyltransferase (CT) activities in transfected cell lines were decreased in proportion to the level of expression of PEMT2. Immunoblot analyses showed a decrease in CT mass as a function of PEMT2 expression. In contrast, there was no change in the mass of protein disulphide-isomerase or the relative amounts of most proteins expressed in the PEMT2-transfected, compared with control, cells. Similarly, the expression of CT mRNA was decreased in PEMT2-expressing cells, whereas the mRNAs for protein disulphide-isomerase and actin were unchanged. When cell growth was slowed by incubating McArdle-RH7777 cells at 25 degrees C, compared with 37 degrees C, there was no difference in the specific activity of the CT. These results argue that PEMT2 expression down-regulates the CDP-choline pathway by decreasing the expression of the gene for the CT. The decreased activity of the CDP-choline pathway might contribute to the slower rate of cell division in PEMT2-transfected hepatoma cells./p
机译:大鼠肝脏的磷脂酰乙醇胺N-甲基转移酶-2(PEMT2)在缺乏内源性PEMT活性的McArdle-RH7777大鼠肝癌细胞中表达。通过测定PEMT活性和免疫印迹证实了该酶的表达。在转染的细胞中,磷脂酰胆碱的量没有变化[Cu,Houweling和Vance(1994)J.Biol.Chem.Soc。,1992,5,1897]。化学269,24531-24533],即使PEMT2的表达引起[甲基-3H]蛋氨酸和[3H]乙醇胺向磷脂酰胆碱中的掺入增加。相反,[3H]丝氨酸掺入磷脂酰胆碱仅通过PEMT2表达略微增强。 [甲基-3H]胆碱掺入磷脂酰胆碱的作用降低了60%以上,表明CDT-胆碱途径被PEMT2表达抑制。转染的细胞系中的CTP:磷酸胆碱胞苷转移酶(CT)活性与PEMT2的表达水平成比例地降低。免疫印迹分析显示,CT量减少与PEMT2表达有关。相比之下,与对照细胞相比,转染PEMT2的蛋白质二硫键异构酶的质量或大多数蛋白质的相对量没有变化。同样,在表达PEMT2的细胞中CT mRNA的表达降低,而蛋白质二硫键异构酶和肌动蛋白的mRNA则保持不变。与37摄氏度相比,通过在25摄氏度下孵育McArdle-RH7777细胞来减慢细胞生长时,CT的比活没有差异。这些结果表明,PEMT2的表达通过减少CT基因的表达而下调CDP-胆碱途径。 CDP-胆碱途径的活性降低可能是导致PEMT2转染的肝癌细胞中细胞分裂速度减慢的原因。

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