共 50 条
Effect of inoculum density on human-induced pluripotent stem cell expansion in 3D bioreactors
被引:14
作者:
Greuel, Selina
[1
]
Hanci, Guengoer
[1
]
Boehme, Mike
[1
]
Miki, Toshio
[2
]
Schubert, Frank
[3
]
Sittinger, Michael
[4
]
Mandenius, Carl-Fredrik
[5
]
Zeilinger, Katrin
[1
]
Freyer, Nora
[1
]
机构:
[1] Charite Univ Med Berlin, Bioreactor Grp, Berlin Brandenburg Ctr Regenerat Therapies BCRT, Berlin, Germany
[2] Univ Southern Calif, Keck Sch Med, Dept Surg, Los Angeles, CA USA
[3] StemCell Syst GmbH, Berlin, Germany
[4] Charite Univ Med Berlin, Dept Rheumatol & Clin Immunol, Berlin Brandenburg Ctr Regenerat Therapies BCRT, Tissue Engn Lab, Berlin, Germany
[5] Linkoping Univ, Dept Phys Chem & Biol IFM, Div Biotechnol, Linkoping, Sweden
关键词:
3D culture;
bioreactor culture;
cell expansion;
human-induced pluripotent stem cells;
inoculum density;
EXTRACORPOREAL LIVER SUPPORT;
3-DIMENSIONAL PERFUSION;
GENE-EXPRESSION;
SUSPENSION-CULTURE;
DIFFERENTIATION;
PATIENT;
GENERATION;
SYSTEMS;
D O I:
10.1111/cpr.12604
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Objective For optimized expansion of human-induced pluripotent stem cells (hiPSCs) with regards to clinical applications, we investigated the influence of the inoculum density on the expansion procedure in 3D hollow-fibre bioreactors. Materials and Methods Analytical-scale bioreactors with a cell compartment volume of 3 mL or a large-scale bioreactor with a cell compartment volume of 17 mL were used and inoculated with either 10 x 10(6) or 50 x 10(6) hiPSCs. Cells were cultured in bioreactors over 15 days; daily measurements of biochemical parameters were performed. At the end of the experiment, the CellTiter-Blue (R) Assay was used for culture activity evaluation and cell quantification. Also, cell compartment sections were removed for gene expression and immunohistochemistry analysis. Results The results revealed significantly higher values for cell metabolism, cell activity and cell yields when using the higher inoculation number, but also a more distinct differentiation. As large inoculation numbers require cost and time-extensive pre-expansion, low inoculation numbers may be used preferably for long-term expansion of hiPSCs. Expansion of hiPSCs in the large-scale bioreactor led to a successful production of 5.4 x 10(9) hiPSCs, thereby achieving sufficient cell amounts for clinical applications. Conclusions In conclusion, the results show a significant effect of the inoculum density on cell expansion, differentiation and production of hiPSCs, emphasizing the importance of the inoculum density for downstream applications of hiPSCs. Furthermore, the bioreactor technology was successfully applied for controlled and scalable production of hiPSCs for clinical use.
引用
收藏
页数:12
相关论文
共 50 条