HEK 293细胞
生物
胚胎干细胞
细胞生物学
细胞培养
活力测定
下调和上调
遗传增强
基因
生物化学
遗传学
作者
Shunsuke Shiina,Nobuyoshi Nagao,Junichi Hasegawa,Tori Sato,Chisato Mori,Kaya Ohtaki,Kiyomi Kubodera,Yuri Yamashita,Kazuhisa Tanabe,Yasuhiro Kawano,Haruhiko Aoyagi
标识
DOI:10.1016/j.jbiosc.2022.07.006
摘要
Investigation of enhancers to improve recombinant adeno-associated virus 2 (rAAV2) productivity by human embryonic kidney 293 cells (HEK293) suspension culture showed that the addition of ethanol improved the productivity and packaged genome integrity of rAAV2. Further optimization showed that adding ethanol in the range of 0.09%-1.11% (v/v) during rAAV2 production effectively improved rAAV2 productivity and quality. In addition, ethanol addition improved cell viability. Furthermore, proteome and pathway analysis of the cells during rAAV2 production showed that the addition of ethanol resulted in the upregulation of pathways related to intercellular signaling, gene expression, cell morphology, intercellular maintenance, and others. In contrast, pathways related to cell death, immunity, and reactions to infection were downregulated. These changes in pathway regulation were responsible for the improvement in rAAV2 productivity, packaged genome integrity, and cell viability during rAAV2 production. The results of this study can be applied to the production of viral vectors for in vivo gene therapy in an inexpensive and safe manner.
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