Optimization of initial culture stage of Vero and HEK293 cell lines
https://doi.org/10.47183/mes.2025-324
Abstract
Introduction. Laboratory production of viral material in small quantities is performed, as a rule, using adherent cell lines and culture flasks of varying surface area. The need to increase product yield leads to either an increase in the number of flasks or a switch to other accumulation systems, such as roller bottles. One factor influencing the efficiency of cell adhesion and homogeneous monolayer formation is the rotation frequency of the roller bottle. There is a lack of available research data on the impact of rotation frequency on these parameters and determination of its optimal value, particularly based on cellular morphology.
Objective. To optimize the initial stage of roller cultivation for Vero and HEK293 cell lines, taking into account the effect of roller bottle rotation frequency on cell adhesion during seeding and monolayer formation.
Materials and methods. Experiments were conducted using two monolayer cell lines, Vero and HEK293. Seeding concentrations were taken from the cell line passports, amounting to 4×104 cells/cm2. Each cell line was seeded onto roller bottles and cultured according to the range of rotation frequencies (0.2, 0.3, 0.4, 0.5, and 0.6 rpm) using a Celrol Mid roller (Wiggens) in a RWD D180 CO2 incubator. Following 1, 2, and 3 days of cultivation, the quality of cell adherence to the growth surface and monolayer formation was assessed by a TC5400 microscope (Meiji Techno).
Results. During cultivation of the Vero cell line, the rotation frequency up to 0.6 rpm did not significantly affect cell adhesion to the surface. The most homogenous cell distribution was observed at rotation frequencies of 0.4–0.5 rpm. The HEK293 cell culture is more sensitive to mechanical disturbances of the nutrient medium; as a result, at rotation frequencies above 0.2 rpm, abnormally rounded cell shapes and impaired adherence to the growth surface were observed. Furthermore, continued cultivation at this rotation frequency did not lead to the formation of a homogenous monolayer due to slow alternation between the respiration and nutrition phases. Consequently, after cell adherence to the surface, the rotation frequency of the roller bottle should be increased.
Conclusions. For the Vero cell line, the optimal rotation frequency was established to be 0.4–0.5 rpm. For the HEK293 cell line, the rotation frequency should be at least 0.2 rpm during the first day followed by its increase to 0.5 rpm after 24 h. The tested cultivation conditions enable an efficient growth of these cell lines for the production of viral biomass.
About the Authors
I. I. TuzovaRussian Federation
Irina I. Tuzova
Moscow
T. I. Chirkina
Russian Federation
Tatyana I. Chirkina
Moscow
I. A. Churkin
Russian Federation
Igor A. Churkin
Moscow
A. N. Lyakh
Russian Federation
Anastasia N. Lyakh
Moscow
K. M. Mefed
Russian Federation
Kirill M. Mefed
Moscow
V. A. Maximov
Russian Federation
Vladimir A. Maximov
Moscow
References
1. Shen CF, Guilbault C, Li X, Elahi SM, Ansorge S, Kamen A, et al. Development of suspension adapted Vero cell culture process technology for production of viral vaccines. Vaccine. 2019;37(47):6996–7002. https://doi.org/10.1016/j.vaccine.2019.07.003
2. Sеne M-A, Xia Y, Kamen AA. Overview of recent advances in Vero cells genomic characterization and engineering for high-throughput vaccine manufacturing. Clinical and Translational Discovery. 2022;2(2):1–6. https://doi.org/10.1002/ctd2.40
3. Kiesslich S, Kamen А. Vero cell upstream bioprocess development for the production of viral vectors and vaccines. Biotechnology Advances. 2020;44:1–9. https://doi.org/10.1016/j.biotechadv.2020.107608
4. Malm M, Saghaleyni R, Lundqvist M, Giudici M, Chotteau V, Field R, et al. Evolution from adherent to suspension: systems biology of HEK293 cell line development. Scientific Reports. 2020;10:18996. https://doi.org/10.1038/s41598-020-76137-8
5. Tan E, Chin CSH, Lim ZFS, Ng SK. HEK293 Cell Line as a Platform to Produce Recombinant Proteins and Viral Vectors. Frontiers in Bioengineering and Biotechnology. 2021;9:796991. https://doi.org/10.3389/fbioe.2021.796991
6. Morozov AN, Yakhin IR, Stratonova NV, Kutskir MV, Poteryaev DA, Khamitov RA. An experience of scaling and intensifying the industrial production of the Gam-COVID-Vac vector adenovirus vaccine in the limiting conditions of the pandemic. Biological Products. Prevention, Diagnosis, Treatment. 2022;22(4):382–91 (In Russ.) https://doi.org/10.30895/2221-996X-2022-22-4-382-391
7. Ishmukhametov AA. Fundamental and applied sciences, technology, and immunobiological products. Herald of the Russian Academy of Sciences. 2022;92(8):717–21 (In Russ.). https://doi.org/10.31857/S0869587322080059
8. Babak VA, Lomako YuV, Gusev AA, Chaplygo KEH, Puntus IA, Filipkova AE. Optimal cultivation conditions for the BHK-21 cell line (c-13). Transactions of the educational establishment “Vitebsk the Order of “the Badge of Honor” State Academy of Veterinary Medicine. 2011;47(2–1):7–11 (In Russ.). EDN: SHRRRD
9. Ryabova EI, Derkaev AA, Esmagambetov IB, Shcheblyakov DV, Dovgiy MA, Byrikhina DV, et al. Comparison of different technologies for producing recombinant adeno-associated virus on a laboratory scale. BIOpreparations. Prevention, Diagnosis, Treatment. 2021;21(4):266–78 (In Russ.). https://doi.org/10.30895/2221-996X-2021-21-4-266-278
10. Bellani CF, Ajeian J, Duffy L, Miotto M, Groenewegen L, Connon CJ. Scale-Up Technologies for the Manufacture of Adherent Cells. Frontiers in Nutrition. 2020;7:575146. https://doi.org/10.3389/fnut.2020.575146
11. Sedova ES, Shcherbinin DN, Bandelyuk AS, Verkhovskaya LV, Viskova NYu, Avdonina ED, et al. Method for obtaining recombinant antibodies produced by a cell line transduced with recombinant adenoviruses. Fine Chemical Technologies. 2023;18(1):48–64 (In Russ.). https://doi.org/10.32362/2410-6593-2023-18-1-48-64
12. Yang J, Guertin P, Jia G, Lv Z, Yang H, Ju D. Large-scale microcarrier culture of HEK293T cells and Vero cells in single-use bioreactors. Applied and Industrial Microbiology. 2019;9(70):1–14. https://doi.org/10.1186/s13568-019-0794-5
13. Reshetnikova OV. Biotechnology of virus cultivation. Current Issues in the Theory and Practice of Modern Biotechnology. 2015:155–61 (In Russ.). EDN: XDGYLH
14. Alexander MH. In vitro expansion of postpartum-derived cells in roller bottles. Patent of United States No. 8741638B2; 2014.
15. Generalov SV, Abramova EG, Matveeva ZhV, Zhulidov IM, Savitskaya LV, Lobovikova OA. Optimization of specifications for scaled-up fixed rabies virus cultivation (“Moscow 3253” strain) in Vero cell culture. Problems of Particularly Dangerous Infections. 2014;2:101–3 (In Russ.). https://doi.org/10.21055/0370-1069-2014-2-101-103
16. Liu YL, Wagner K, Robinson N, Sabatino D, Margaritis P, Xiao W, et al. Optimized Production of High-Titer Recombinant Adeno-Associated Virus in Roller Bottles. BioTechniques. 2003;34(1):184–9. https://doi.org/10.2144/03341dd07
17. Chisti Y. Hydrodynamic Damage to Animal Cells. Critical Reviews in Biotechnology. 2001;21(2):67–110. https://doi.org/10.1080/20013891081692
18. Chang HY, Kao WL, You YW, Chu YH, Chu KJ, Chen PJ, et al. Effect of surface potential on epithelial cell adhesion, proliferation and morphology. Colloids and Surfaces B: Biointerfaces. 2016;141:179–86. https://doi.org/10.1016/j.colsurfb.2016.01.049
Supplementary files
Review
For citations:
Tuzova I.I., Chirkina T.I., Churkin I.A., Lyakh A.N., Mefed K.M., Maximov V.A. Optimization of initial culture stage of Vero and HEK293 cell lines. Extreme Medicine. (In Russ.) https://doi.org/10.47183/mes.2025-324








