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Ectoine enhances recombinant antibody production in Chinese hamster ovary cells by promoting cell cycle arrest.
- Source :
-
New Biotechnology . Nov2024, Vol. 83, p56-65. 10p. - Publication Year :
- 2024
-
Abstract
- Chinese hamster ovary (CHO) cells represent the most preferential host cell system for therapeutic monoclonal antibody (mAb) production. Enhancing mAb production in CHO cells can be achieved by adding chemical compounds that regulate the cell cycle and cell survival pathways. This study investigated the impact of ectoine supplementation on mAb production in CHO cells. The results showed that adding ectoine at a concentration of 100 mM on the 3rd day of cultivation improved mAb production by improving cell viability and extending the culture duration. RNA sequencing analysis revealed differentially expressed genes associated with cell cycle regulation, cell proliferation, and cellular homeostasis, in particular promotion of cell cycle arrest, which was then confirmed by flow cytometry analysis. Ectoine-treated CHO cells exhibited an increase in the number of cells in the G0/G1 phase. In addition, the cell diameter was also increased. These findings support the hypothesis that ectoine enhances mAb production in CHO cells through mechanisms involving cell cycle arrest and cellular homeostasis. Overall, this study highlights the potential of ectoine as a promising supplementation strategy to enhance mAb production not only in CHO cells but also in other cell lines. [Display omitted] • Ectoine improved mAb production in CHO cells. • Ectoine improved cell viability and extended the culture duration of CHO cells. • Ectoine increased the number of CHO cells in the G0/G1 phase. • Enhanced mAb production involved cell cycle arrest and cellular homeostasis. • Ectoine is a promising supplement to enhance mAb production in cell lines. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 18716784
- Volume :
- 83
- Database :
- Academic Search Index
- Journal :
- New Biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 179500072
- Full Text :
- https://doi.org/10.1016/j.nbt.2024.06.006