| Literature DB >> 32996001 |
Ryou Nakanuma1, Kyoko Masumi-Koizumi1, Yuki Ohmuro-Matsuyama1, Tomohisa Katsuda1, Hideki Yamaji2.
Abstract
Insect cells have recently proven to be an excellent platform for the high-level production of functional recombinant proteins. Autophagy is an important mechanism that promotes cell survival by eliminating damaged organelles and protein aggregates, and it also may influence recombinant protein production. In the present study, we compared the effects that autophagy inducers rapamycin, everolimus, and lithium chloride exert on recombinant lepidopteran insect cells that secrete an engineered antibody molecule. Compared with nontreatment, treatment with either rapamycin or everolimus prolonged cell growth to allow high cell density, improved viability in the declining phase, and then increased the yield of secreted antibodies. These positive effects appeared to be induced via autophagy since autophagosomes were clearly detected, particularly in cells treated with rapamycin or everolimus. Unlike rapamycin, another autophagy inducer, FK506, was ineffective in insect cells. The addition of an appropriate autophagy inducer may be effective in increasing the productivity of recombinant proteins in insect cells.Entities:
Keywords: Autophagy inducer; Everolimus; Insect cell culture; Lithium chloride; Rapamycin; Recombinant protein production
Year: 2020 PMID: 32996001 PMCID: PMC8166964 DOI: 10.1007/s10616-020-00423-6
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.040