Integrated culture platform based on a human platelet lysate supplement for the isolation and scalable manufacturing of umbilical cord matrix-derived mesenchymal stem/stromal cells

被引:39
作者
de Soure, Antonio M. [1 ,2 ]
Fernandes-Platzgummer, Ana [1 ,2 ]
Moreira, Francisco [1 ,2 ]
Lilaia, Carla [3 ]
Liu, Shi-Hwei [4 ]
Ku, Chen-Peng [4 ,5 ]
Huang, Yi-Feng [4 ,5 ]
Milligan, William [4 ,5 ]
Cabral, Joaquim M. S. [1 ,2 ]
da Silva, Claudia L. [1 ,2 ]
机构
[1] Univ Lisbon, Dept Bioengn, Ave Rovisco Pais, P-1049001 Lisbon, Portugal
[2] Univ Lisbon, Inst Super Tecn, iBB Inst Bioengn & Biosci, Ave Rovisco Pais, P-1049001 Lisbon, Portugal
[3] Hosp Sao Francisco Xavier, Ctr Hosp Lisboa Ocidental, Lisbon, Portugal
[4] AventaCell BioMed Co Ltd, R&D, New Taipei, Taiwan
[5] AventaCell BioMed Co Ltd, R&D, Atlanta, GA USA
关键词
mesenchymal stem/stromal cells; ex vivo expansion; microcarriers; xenogeneic-free; human platelet lysate; umbilical cord matrix; stem cell isolation; scale-up; STEM-CELLS; EXPANSION; CAPACITY;
D O I
10.1002/term.2200
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Umbilical cord matrix (UCM)-derived mesenchymal stem/stromal cells (MSCs) are promising therapeutic candidates for regenerative medicine settings. UCM MSCs have advantages over adult cells as these can be obtained through a noninvasive harvesting procedure and display a higher proliferative capacity. However, the high cell doses required in the clinical setting make large-scale manufacturing of UCM MSCs mandatory. A commercially available human platelet lysate-based culture supplement (UltraGRO(TM), AventaCell BioMedical) (5%(v/v)) was tested to effectively isolate UCM MSCs and to expand these cells under (1) static conditions, using planar culture systems and (2) stirred culture using plastic microcarriers in a spinner flask. The MSC-like cells were isolated from UCM explant cultures after 11 +/- 2 days. After five passages in static culture, UCM MSCs retained their immunophenotype and multilineage differentiation potential. The UCM MSCs cultured under static conditions using UltraGRO(TM)-supplemented medium expanded more rapidly compared with UCM MSCs expanded using a previously established protocol. Importantly, UCM MSCs were successfully expanded under dynamic conditions on plastic microcarriers using UltraGRO TM -supplemented medium in spinner flasks. Upon an initial 54% cell adhesion to the beads, UCM MSCs expanded by >13-fold after 5-6 days, maintaining their immunophenotype and multilineage differentiation ability. The present paper reports the establishment of an easily scalable integrated culture platform based on a human platelet lysate supplement for the effective isolation and expansion of UCM MSCs in a xenogeneic-free microcarrier-based system. This platform represents an important advance in obtaining safer and clinically meaningful MSC numbers for clinical translation. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:1630 / 1640
页数:11
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