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Transient gene expression in mammalian cells grown in serum-free suspension culture

机译:在无血清悬浮培养中生长的哺乳动物细胞中的瞬时基因表达

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In order to establish a simple and scaleable transfection system we have used the cationic polymer polyethylenimine (PEI) to study transient transfection in HEK293 and 293(EBNA) cells grown in serum-free suspension culture. The transfection complexes were made directly within the cell culture by consecutively adding plasmid and PEI (direct method). Alternatively, the DNA-PEI transfection complexes were prepared in fresh medium (1/10 culture volume) and then added to the cells (indirect method). The results of this study clearly show that the ratio of PEI nitrogen to DNA phosphate is very important for high expression levels. The precise ratio is dependent on the DNA concentration. For example, using 1 μg/ml DNA by the indirect method, the ratio of optimal PEI:DNA was about 10–13:1. However, the ratio increases to 33:1 for 0.1–0.2 μg/ml DNA. By testing several different molecular weights of the polycationic polymer we could show that the highest transfection efficiency was obtained with the PEI 25 kDa. Using PEI 25 kDa the indirect method is superior to the direct addition because significantly lower DNA concentrations are needed. The expression levels of the soluble human TNF receptor p55 are even higher at low DNA compared to 1 μg/ml plasmid. The EBV-based pREP vectors gave better transient gene expression when used in 293(EBNA) cells compared to HEK293 cells in suspension culture. No differences in expression levels in the two cell lines were observed when the pC1 (CMV)-TNFR was used. In conclusion, PEI is a low-toxic transfection agent which provides high levels of transient gene expression in 293(EBNA) cells grown in serum-free suspension culture. This system allows highly reproducible, cost-effective production of milligram amounts of recombinant proteins in 2–5 l spinner culture scale within 3–5 days. Fermentor scale experiments, however, are less efficient because the PEI-mediated transient tranfection is inhibited by conditioned medium.
机译:为了建立简单且可扩展的转染系统,我们使用了阳离子聚合物聚乙烯亚胺(PEI)研究无血清悬浮培养中生长的HEK293和293(EBNA)细胞中的瞬时转染。通过连续添加质粒和PEI(直接方法),直接在细胞培养物中制备转染复合物。或者,在新鲜培养基(1/10培养体积)中制备DNA-PEI转染复合物,然后添加到细胞中(间接方法)。这项研究的结果清楚地表明,PEI氮与DNA磷酸盐的比例对于高表达水平非常重要。精确比例取决于DNA浓度。例如,通过间接方法使用1μg/ ml DNA,最佳PEI:DNA的比例约为10–13:1。但是,对于0.1–0.2μg/ ml DNA,该比率增加到33:1。通过测试几种不同分子量的聚阳离子聚合物,我们可以证明,PEI 25 kDa可获得最高的转染效率。使用PEI 25 kDa时,间接法优于直接法,因为需要低得多的DNA浓度。与1μg/ ml质粒相比,在低DNA下可溶性人TNF受体p55的表达水平甚至更高。与悬浮培养中的HEK293细胞相比,基于EBV的pREP载体在293(EBNA)细胞中使用时具有更好的瞬时基因表达。使用pC1(CMV)-TNFR时,在两种细胞系中均未观察到表达水平的差异。总之,PEI是一种低毒转染剂,可在无血清悬浮培养物中生长的293(EBNA)细胞中提供高水平的瞬时基因表达。该系统可在3-5天之内以2–5 l旋转培养规模生产高度可重复,经济高效的毫克级重组蛋白。然而,发酵罐规模的实验效率较低,因为条件培养基抑制了PEI介导的瞬时转染。

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