Effects of manipulating lactate dehydrogenase gene on metabolism of HEK-293 and production of human adenovirus.
- Author:
Junqing MIAO
1
;
Xiaoping YI
1
;
Xiangchao LI
1
;
Yingping ZHUANG
1
Author Information
- Publication Type:Journal Article
- Keywords: energy metabolism; human adenovirus (HAdV); human embryonic kidney 293 cells (HEK-293); lactate dehydrogenase (LDH); substrate metabolism
- MeSH: Animals; Humans; L-Lactate Dehydrogenase/genetics*; Lactic Acid; Adenoviruses, Human; Ammonia; HEK293 Cells; Glucose/metabolism*; Adenosine Triphosphate/metabolism*; Kidney/metabolism*; Mammals/metabolism*
- From: Chinese Journal of Biotechnology 2023;39(9):3863-3875
- CountryChina
- Language:Chinese
- Abstract: Reducing lactate accumulation has always been a goal of the mammalian cell biotechnology industry. When animal cells are cultured in vitro, the accumulation of lactate is mainly the combined result of two metabolic pathways. On one hand, glucose generates lactate under the function of lactate dehydrogenase A (LDHA); on the other hand, lactate can be oxidized to pyruvate by LDHB or LDHC and re-enter the TCA cycle. This study comprehensively evaluated the effects of LDH manipulation on the growth, metabolism and human adenovirus (HAdV) production of human embryonic kidney 293 (HEK-293) cells, providing a theoretical basis for engineering the lactate metabolism in mammalian cells. By knocking out ldha gene and overexpression of ldhb and ldhc genes, the metabolic efficiency of HEK-293 cells was effectively improved, and HAdV production was significantly increased. Compared with the control cell, LDH manipulation promoted cell growth, reduced the accumulation of lactate and ammonia, significantly enhanced the efficiency of substrate and energy metabolism of cells, and significantly increased the HAdV production capacity of HEK-293 cells. Among these LDH manipulation measures, ldhc gene overexpression performed the best, with the maximum cell density increased by about 38.7%. The yield of lactate to glucose and ammonia to glutamine decreased by 33.8% and 63.3%, respectively; and HAdV titer increased by at least 16 times. In addition, the ATP production rate, ATP/O2 ratio, ATP/ADP ratio and NADH content of the modified cell lines were increased to varying degrees, and the energy metabolic efficiency was significantly improved.
