Expansion of 3D human induced pluripotent stem cell aggregates in bioreactors: Bioprocess intensification and scaling-up approaches

被引:66
|
作者
Abecasis, Bernardo [1 ,2 ]
Aguiar, Tiago [1 ,2 ]
Arnault, Emilie [1 ,2 ]
Costa, Rita [1 ,2 ]
Gomes-Alves, Patricia [1 ,2 ]
Aspegren, Anders [3 ]
Serra, Margarida [1 ,2 ]
Alves, Paula M. [1 ,2 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol Antonio Xavier, Av Republ, P-2780157 Oeiras, Portugal
[2] iBET, Apartado 12, P-2780901 Oeiras, Portugal
[3] Takara Bio Europe AB, Arvid Wallgrens Backe 20, SE-41346 Gothenburg, Sweden
关键词
Human induced pluripotent stem cells; Stirred tank bioreactors; Aggregate dissociation; Continuous expansion; Scale-up; Whole proteome; SUSPENSION-CULTURE; HUMAN LIVER; DIFFERENTIATION; METABOLISM; PERFUSION; THERAPY; PROMISE;
D O I
10.1016/j.jbiotec.2017.01.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human induced pluripotent stem cells (hiPSC) are attractive tools for drug screening and disease modeling and promising candidates for cell therapy applications. However, to achieve the high numbers of cells required for these purposes, scalable and clinical-grade technologies must be established. In this study, we use environmentally controlled stirred-tank bioreactors operating in perfusion as a powerful tool for bioprocess intensification of hiPSC production. We demonstrate the importance of controlling the dissolved oxygen concentration at low levels (4%) and perfusion at 1.3 day(-1) dilution rate to improve hiPSC growth as aggregates in a xeno-free medium. This strategy allowed for increased cell specific growth rate, maximum volumetric concentrations (4.7 x 10(6) cell/mL) and expansion factors (approximately 19 in total cells), resulting in a 2.6-fold overall improvement in cell yields. Extensive cell characterization, including whole proteomic analysis, was performed to confirm that cells' pluripotent phenotype was maintained during culture. A scalable protocol for continuous expansion of hiPSC aggregates in bioreactors was implemented using mechanical dissociation for aggregate disruption and cell passaging. A total expansion factor of 1100 in viable cells was obtained in 11 days of culture, while cells maintained their proliferation capacity, pluripotent phenotype and potential as well as genomic stability after 3 sequential passages in bioreactors. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 93
页数:13
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