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Enhanced lentiviral vector production in 293FT cells expressing Siglec-9

机译:表达Siglec-9的293FT细胞中增强的慢病毒载体生产

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摘要

Siglecs, sialic acid-recognizing Ig-superfamily lectins, regulate various aspects of immune responses, and have also been shown to induce the endocytosis of binding materials such as anti-Siglec antibodies or sialic acid-harboring bacteria. In this study, we demonstrated that the expression of Siglec-9 enhanced the transfection efficiency of several cell lines such as macrophage RAW264 and non-hematopoietic 293FT cells. We applied this finding to the production of a lentiviral vector in which cells were transfected simultaneously with multiple vectors, and achieved a twice increase in viral production levels. Furthermore, 293FT cells expressing lectin-defective Siglec-9 produced three- to seven-fold higher titer of viral vector compared with parental 293FT cells. These results suggest that Siglec-9 enhanced lentiviral vector production in a lectin-independent manner.
机译:Siglecs,可识别唾液酸的Ig超家族凝集素,可调节免疫应答的各个方面,并且还显示出可诱导结合材料(例如抗Siglec抗体或唾液酸携带细菌)的内吞作用。在这项研究中,我们证明了Siglec-9的表达增强了多种细胞系的转染效率,例如巨噬细胞RAW264和非造血293FT细胞。我们将这一发现应用于慢病毒载体的生产中,其中用多种载体同时转染了细胞,并实现了病毒生产水平的两倍提高。而且,与亲本293FT细胞相比,表达凝集素缺陷型Siglec-9的293FT细胞产生的病毒载体滴度高3至7倍。这些结果表明,Siglec-9以凝集素非依赖性方式增强了慢病毒载体的产生。

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