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Enhancement of Human Prolactin Synthesis by Sodium Butyrate Addition to Serum-Free CHO Cell Culture

机译:无血清CHO细胞培养液中加入丁酸钠增强人催乳素的合成

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摘要

Sodium butyrate (NaBu) has been used as a productivity enhancer for the synthesis of recombinant proteins in Chinese hamster ovary (CHO) cells. Thus, the influence of NaBu on the production of recombinant human prolactin (hPRL) from CHO cells was investigated for the first time. CHO cell cultures were submitted to a treatment with different concentrations of NaBu (0.25 to 4 mM). Quantitative and qualitative analyses by reverse-phase high-performance liquid chromatography (RP-HPLC) and Western blot or SDS-PAGE, carried out directly on CHO-conditioned medium, showed that the highest hPRL expression was obtained with 1 mM NaBu. In vitro biological assays based on noble rat lymphoma (Nb2) and mouse pro-B lymphoma (Ba/F3-LLP) cells were carried out on purified hPRL. Its bioactivity in the presence of NaBu was not apparently different from that of the First International Reference Reagent of recombinant hPRL (WHO 97/714). Our results show that NaBu increased the synthesis of recombinant hPRL in CHO cells, apparently without compromising either its structure or function.
机译:丁酸钠(NaBu)已被用作生产力增强剂,用于在中国仓鼠卵巢(CHO)细胞中合成重组蛋白。因此,首次研究了NaBu对从CHO细胞产生重组人催乳素(hPRL)的影响。 CHO细胞培养物接受不同浓度的NaBu(0.25至4μmM)处理。直接在CHO条件培养基上进行的反相高效液相色谱(RP-HPLC)和Western blot或SDS-PAGE定量和定性分析表明,hPRL的表达是用1μmMNaBu获得的。在纯化的hPRL上进行了基于贵族大鼠淋巴瘤(Nb2)和小鼠pro-B淋巴瘤(Ba / F3-LLP)细胞的体外生物学测定。在NaBu存在下,其生物活性与重组hPRL的第一个国际参考试剂(WHO 97/714)并无明显差异。我们的结果表明,NaBu可以在CHO细胞中增加重组hPRL的合成,显然不会损害其结构或功能。

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