Research Laboratories, F. Hoffmann La Roche Ltd., CH-4070, Basel, Switzerland.
Cytotechnology. 1999 Jul;30(1-3):71-83. doi: 10.1023/A:1008000327766.
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 mug/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 mug/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 mug/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.
为了建立一个简单而可扩展的转染系统,我们使用阳离子聚合物聚乙烯亚胺(PEI)来研究在无血清悬浮培养中生长的 HEK293 和 293(EBNA)细胞中的瞬时转染。转染复合物通过连续向细胞培养物中添加质粒和 PEI(直接法)直接在细胞内制成。或者,将 DNA-PEI 转染复合物在新鲜培养基(培养体积的 1/10)中制备,然后添加到细胞中(间接法)。本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。精确的比例取决于 DNA 浓度。例如,使用间接法的 1 μg/ml DNA,最佳 PEI:DNA 的比例约为 10-13:1。然而,对于 0.1-0.2 μg/ml DNA,该比例增加到 33:1。通过测试几种不同分子量的多阳离子聚合物,我们可以证明使用 PEI 25 kDa 可获得最高的转染效率。使用 PEI 25 kDa,间接法优于直接添加,因为需要的 DNA 浓度要低得多。与 1 μg/ml 质粒相比,在低 DNA 浓度下,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)细胞中使用时可提供更好的瞬时基因表达。当使用 pC1(CMV)-TNFR 时,在这两种细胞系中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中生长的 293(EBNA)细胞中提供高水平的瞬时基因表达。该系统允许在 2-5 升搅拌器培养规模内在 3-5 天内以高重复性、具有成本效益的方式生产毫克量的重组蛋白。然而,由于条件培养基抑制 PEI 介导的瞬时转染,发酵罐规模的实验效率较低。