de Soure António M, Fernandes-Platzgummer Ana, Moreira Francisco, Lilaia Carla, Liu Shi-Hwei, Ku Chen-Peng, Huang Yi-Feng, Milligan William, Cabral Joaquim M S, da Silva Cláudia L
Department of Bioengineering and iBB-, Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Lisboa, Portugal.
Hospital São Francisco Xavier, Centro Hospitalar Lisboa Ocidental, Lisboa, Portugal.
J Tissue Eng Regen Med. 2017 May;11(5):1630-1640. doi: 10.1002/term.2200. Epub 2016 Jul 22.
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 non-invasive 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 , 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 -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 -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 © 2016 John Wiley & Sons, Ltd.
脐带基质(UCM)来源的间充质干/基质细胞(MSCs)是再生医学领域很有前景的治疗候选细胞。UCM MSCs比成体细胞具有优势,因为它们可以通过非侵入性采集程序获得,并且具有更高的增殖能力。然而,临床环境中所需的高细胞剂量使得大规模生产UCM MSCs成为必需。测试了一种市售的基于人血小板裂解物的培养补充剂(UltraGRO ,AventaCell生物医学公司)(5%(v/v)),以有效地分离UCM MSCs,并在(1)静态条件下,使用平面培养系统,以及(2)在转瓶中使用塑料微载体进行搅拌培养的条件下扩增这些细胞。在11±2天后从UCM外植体培养物中分离出MSC样细胞。在静态培养传代五次后,UCM MSCs保留了它们的免疫表型和多向分化潜能。与使用先前建立的方案扩增的UCM MSCs相比,使用补充了UltraGRO的培养基在静态条件下培养的UCM MSCs扩增得更快。重要的是,使用补充了UltraGRO的培养基,UCM MSCs在转瓶中的塑料微载体上在动态条件下成功扩增。在最初54%的细胞附着于微珠后,UCM MSCs在5-6天后扩增了超过13倍,同时保持其免疫表型和多向分化能力。本文报道了基于人血小板裂解物补充剂建立的一个易于扩大规模的综合培养平台,用于在无异种动物成分的基于微载体的系统中有效分离和扩增UCM MSCs。该平台在获得更安全且具有临床意义的MSC数量以用于临床转化方面代表了一项重要进展。版权所有© 2016约翰威立父子有限公司。