Oxidative stress‐alleviating strategies to improve recombinant protein production in CHO cells
Стратегии снижения окислительного стресса для повышения продукции рекомбинантных белков в клетках CHO
2019-12-09
SCID: 54.1/dpc7yetp
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Chinese hamster ovary cellscell engineeringoxidative stressreactive oxygen speciesrecombinant protein production
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Abstract (AI)
Large scale biopharmaceutical production of biologics relies on the overexpression of foreign proteins by cells cultivated in stirred tank bioreactors. It is well recognized and documented fact that protein overexpression may impact host cell metabolism and that factors associated with large scale culture, such as the hydrodynamic forces and inhomogeneities within the bioreactors, may promote cellular stress. The metabolic adaptations required to support the high-level expression of recombinant proteins include increased energy production and improved secretory capacity, which, in turn, can lead to a rise of reactive oxygen species (ROS) generated through the respiration metabolism and the interaction with media components. Oxidative stress is defined as the imbalance between the production of free radicals and the antioxidant response within the cells. Accumulation of intracellular ROS can interfere with the cellular activities and exert cytotoxic effects via the alternation of cellular components. In this context, strategies aiming to alleviate oxidative stress generated during the culture have been developed to improve cell growth, productivity, and reduce product microheterogeneity. In this review, we present a summary of the different approaches used to decrease the oxidative stress in Chinese hamster ovary cells and highlight media development and cell engineering as the main pathways through which ROS levels may be kept under control.
Key Findings
1
Intracellular ROS accumulation can disrupt cellular functions, damage cellular components, and exert cytotoxic effects.
2
Large-scale culture conditions, including hydrodynamic forces and bioreactor inhomogeneities, may intensify cellular stress and oxidative imbalance.
3
Media development and cell engineering are identified as the main approaches for controlling ROS levels during CHO cell culture.
4
Oxidative-stress mitigation strategies aim to improve CHO cell growth and recombinant protein productivity while reducing product microheterogeneity.
5
Recombinant protein overexpression in CHO cells increases metabolic demands and can elevate reactive oxygen species during bioreactor culture.
Research Object
Chinese hamster ovary (CHO) cells cultivated for recombinant protein production
Research Subject
Strategies for alleviating intracellular oxidative stress and their effects on cell growth, recombinant protein productivity, and product microheterogeneity
Publication Details
Publication Date
2019-12-09
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