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Regulation of cell growth and apoptosis through lactate dehydrogenase C over-expression in Chinese hamster ovary cells

乳酸脱氢酶 丙酮酸钠 中国仓鼠卵巢细胞 细胞凋亡 乳酸钠 细胞培养 生物 细胞生长 丙酮酸 生物化学 分子生物学 程序性细胞死亡 化学 有机化学 遗传学
作者
Tuo Fu,Cunchao Zhang,Yu Jing,Cheng Jiang,Zhenhua Li,Shengyu Wang,Kai Ma,Dapeng Zhang,Sheng Hou,Jianxin Dai,Geng Kou,Hao Wang
出处
期刊:Applied Microbiology and Biotechnology [Springer Science+Business Media]
卷期号:100 (11): 5007-5016 被引量:31
标识
DOI:10.1007/s00253-016-7348-4
摘要

Lactate has long been credited as a by-product, which jeopardizes cell growth and productivity when accumulated over a certain concentration during the manufacturing process of therapeutic recombinant proteins by Chinese hamster ovary (CHO) cells. A number of efforts to decrease the lactate concentration have been developed; however, the accumulation of lactate is still a critical issue by the late stage of fed-batch culture. Therefore, a lactate-tolerant cell line was developed through over-expression of lactate dehydrogenase C (LDH-C). In fed-batch culture, sodium lactate or sodium pyruvate was supplemented into the culture medium to simulate the environment of lactate accumulation, and LDH-C over-expression increased the highest viable cell density by over 30 and 50 %, respectively, on day 5, meanwhile the viability was also improved significantly since day 5 compared with that of the control. The percentages of cells suffering early and late apoptosis decreased by 3.2 to 12.5 and 2.0 to 4.3 %, respectively, from day 6 onwards in the fed-batch culture when 40 mM sodium pyruvate was added compared to the control. The results were confirmed by mitochondrial membrane potential assay. In addition, the expression of cleaved caspases 3 and 7 decreased in cells over-expressing LDH-C, suggesting the mitochondrial pathway was involved in the LDH-C regulated anti-apoptosis. In conclusion, a novel cell line with higher lactate tolerance, lowered lactate production, and alleviated apoptosis response was developed by over-expression of LDH-C, which may potentially represent an efficient and labor-saving approach in generating recombinant proteins.

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