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首页> 外文期刊>Cytotechnology >Characterisation of G418-induced metabolic load in recombinant CHO and BHK cells: effect on the activity and expression of central metabolic enzymes
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Characterisation of G418-induced metabolic load in recombinant CHO and BHK cells: effect on the activity and expression of central metabolic enzymes

机译:重组CHO和BHK细胞中G418诱导的代谢负荷的表征:对中央代谢酶活性和表达的影响

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摘要

In a previous article (Yallop and Svendsen 2001), recombinant CHO and BHK cell lines, expressing the human glucagon receptor and the gastric inhibitory peptide receptor, respectively, showed reduced growth rates and altered nutrient utilisation when grown with increasing concentrations of G418. This response was associated with an increased expression of the neor protein, while expression of the recombinant membrane receptors remained unaltered. The metabolic response was characterised in both cell lines by an increase in the specific rate of glutamine utilisation and in CHO cells by a decrease in the yield of lactate from glucose, suggesting a change in the flux of glucose through central metabolism. The aim of this study was to further elucidate these metabolic changes by determining the activity and relative expression of key enzymes involved in glucose and glutamine metabolism. For both CHO and BHK cells, there was an increase in the activity of glutaminase, glutamate dehydrogenase and glutamine synthetase, suggesting an increased flux through the glutaminolysis pathway. The activity of glucose-6-phosphate dehydrogenase and pyruvate carboxylase in CHO cells was also increased whilst lactate dehydrogenase activity remained unaltered, suggesting an increased flux to the pentose phosphate pathway and TCA cycle, respectively. The activity of these enzymes in BHK cells was unchanged. Quantitative RT-PCR showed that expression levels of glutaminase and pyruvate carboxylase were the same with and without G418, indicating that the differences in activities were likely due to post-translational modifications.
机译:在以前的文章中(Yallop和Svendsen,2001年),重组人CHO和BHK细胞系分别表达人胰高血糖素受体和胃抑制肽受体,但随着G418浓度的增加而生长速度降低,养分利用率也随之改变。该反应与神经蛋白表达的增加有关,而重组膜受体的表达保持不变。两种细胞系中的代谢反应都以谷氨酰胺利用的特定速率增加为特征,而CHO细胞中则以葡萄糖中乳酸的产量降低为特征,表明通过中枢代谢的葡萄糖通量发生了变化。这项研究的目的是通过确定参与葡萄糖和谷氨酰胺代谢的关键酶的活性和相对表达,进一步阐明这些代谢变化。对于CHO和BHK细胞,谷氨酰胺酶,谷氨酸脱氢酶和谷氨酰胺合成酶的活性均增加,表明通过谷氨酰胺分解途径的通量增加。 CHO细胞中的6-磷酸葡萄糖脱氢酶和丙酮酸羧化酶的活性也增加,而乳酸脱氢酶活性保持不变,表明分别增加了戊糖磷酸途径和TCA循环的通量。这些酶在BHK细胞中的活性没有改变。定量RT-PCR显示谷氨酰胺酶和丙酮酸羧化酶的表达水平在有和没有G418的情况下是相同的,表明活性的差异可能是由于翻译后修饰。

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