Effects of blocking apoptosis and lactic acid metabolism pathways on robustness and foreign protein expression of CHO cells.

Hong LU; Tongyang ZHANG; Ruofei LYU; Bolin HOU; Tingwen FAN; Huaiyi YANG; Jie NA

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Effects of blocking apoptosis and lactic acid metabolism pathways on robustness and foreign protein expression of CHO cells.

Author: Hong LU ¹ ; Tongyang ZHANG ² ; Ruofei LYU ¹ ; Bolin HOU ² ; Tingwen FAN ² ; Huaiyi YANG ² ; Jie NA ¹
Author Information

1. School of Life Science, Liaoning Normal University, Dalian 116029, Liaoning, China.
2. CAS Key Laboratory of Microbial Physiological & Metabolic Engineering, State Key Laboratory of Microbial Diversity and Innovative Utilization, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Publication Type:Journal Article
Keywords: Bak; Bax; CHO cell viability; LDHa; tissue plasminogen activator
MeSH: CHO Cells; Cricetulus; Animals; Apoptosis/genetics*; Lactic Acid/metabolism*; Recombinant Proteins/biosynthesis*; L-Lactate Dehydrogenase/genetics*; bcl-2-Associated X Protein/genetics*; bcl-2 Homologous Antagonist-Killer Protein/genetics*; Cricetinae; CRISPR-Cas Systems; Staurosporine/pharmacology*
From: Chinese Journal of Biotechnology 2025;41(8):3098-3109
CountryChina
Language:Chinese
Abstract: The Chinese hamster ovary (CHO) cell is the most representative mammalian cell protein expression system, and it is widely used in recombinant protein, vaccine and other biopharmaceutical fields. However, due to its vulnerability to environmental factors, apoptosis, and metabolic inhibitors, CHO cells demonstrate poor robustness, and thus the integrated viable cell density and unit cell productivity are largely limited. To improve the robustness and foreign protein expression efficiency of CHO cells, we employed CRISPR/Cas9 to knock out the apoptosis genes Bax and Bak and the lactate dehydrogenase gene LDHa, thereby blocking apoptosis and lactic acid metabolism pathways. The results of apoptosis and single cell viability detection showed that the number of apoptotic cells in the knockout cell lines Bax^-/-, Bax-bak^-/-, and LDHa-Bax-bak^-/- was reduced by 22.51%, 37.73%, and 64.12%, respectively, compared with the wild-type cell line CHO-K1, which indicated that the anti-apoptotic ability was significantly improved. After staurosporine treatment, the single cell viability of Bax^-/-, Bax-bak^-/-, and LDHa-Bax-bak^-/- cells was increased by 30.8%, 22%, and 41.1%, respectively. After treatment with puromycin, the single cell viability of Bax^-/-, Bax-bak^-/-, and LDHa-Bax-bak^-/- cells was increased by 26.7%, 30.7%, and 38.8%, respectively. To further investigate the production performance of cells obtained after blocking apoptosis and lactic acid metabolism pathways, we induced transient expression of human tissue plasminogen activator (tPA) in these cells. The results showed that the secretion of tPA in Bax^-/-, Bax-Bak^-/-, and LDHa-Bax-Bak^-/- cells was 11.12%, 46.18%, and 63.13%, respectively, higher than that in wild-type CHO-K1 cells. The expression of intracellular tPA was increased by 35.65%, 130%, and 192.15%. In conclusion, blocking apoptosis and lactic acid metabolism pathways simultaneously can improve cell robustness and productivity, with the performance better than blocking the apoptosis pathway alone. The above results indicated that the constructed cell lines were expected to be the delivery carriers of protein drugs such as medicinal peptides, and better used for the treatment of diseases.