Yang Yuanyuan, Melzer Catharina, Bucan Vesna, von der Ohe Juliane, Otte Anna, Hass Ralf
Department of Obstetrics and Gynecology, Biochemistry and Tumor Biology Laboratory, Hannover Medical School, Carl-Neuberg-Str. 1, Hannover, D-30625, Germany.
Tongji Hospital Affiliated Tongji University, Shanghai, 200065, China.
Stem Cell Res Ther. 2016 Feb 11;7:28. doi: 10.1186/s13287-016-0289-0.
The use of large amounts of human multipotent mesenchymal stroma/stem cells (MSC) for cell therapies represents a desirable property in tissue engineering and banking in the field of regenerative medicine.
Whereas cryo-storage of umbilical cord (UC) tissue pieces in liquid nitrogen without ingredients was associated with predominant appearance of apoptotic cells after thawing and re-culture, progressive growth of MSC was observed following use of cryo-medium. Moreover, conditioning of UC tissue pieces by initial explant culture and subsequent cryo-storage with cryo-medium accelerated a further MSC culture after thawing. These findings suggested that conditioning of UC tissue pieces provides an in vitro stem cell niche by maintenance of a 3-dimensional natural microenvironment for continuous MSC outgrowth and expansion. Indeed, culture of GFP-labeled UC tissue pieces was accompanied by increased outgrowth of GFP-labeled cells which was accelerated in conditioned UC tissue after cryo-storage. Moreover, cryopreserved conditioned UC tissue pieces in cryo-medium after thawing and explant culture could be cryopreserved again demonstrating renewed MSC outgrowth after repeated thawing with similar population doublings compared to the initial explant culture. Flow cytometry analysis of outgrowing cells revealed expression of the typical MSC markers CD73, CD90, and CD105. Furthermore, these cells demonstrated little if any senescence and cultures revealed stem cell-like characteristics by differentiation along the adipogenic, chondrogenic and osteogenic lineages.
Expression of MSC markers was maintained for at least 10 freeze/thaw/explant culture cycles demonstrating that repeated cryopreservation of conditioned UC tissue pieces provided a reproducible and enriched stem cell source.
在再生医学领域,使用大量人类多能间充质基质/干细胞(MSC)进行细胞治疗是组织工程和细胞库中的一个理想特性。
将脐带(UC)组织块在无添加成分的液氮中冷冻保存,解冻并重新培养后主要出现凋亡细胞,而使用冷冻培养基后观察到MSC的逐步生长。此外,通过初始外植体培养和随后用冷冻培养基进行冷冻保存来预处理UC组织块,可加速解冻后的进一步MSC培养。这些发现表明,对UC组织块进行预处理通过维持三维自然微环境以促进MSC持续生长和扩增,从而提供了一个体外干细胞生态位。实际上,绿色荧光蛋白(GFP)标记的UC组织块培养伴随着GFP标记细胞的生长增加,冷冻保存后在预处理的UC组织中这种生长加速。此外,解冻并进行外植体培养后保存在冷冻培养基中的预处理UC组织块可以再次冷冻保存,与初始外植体培养相比,反复解冻后显示出类似的群体倍增且有新的MSC生长。对生长出的细胞进行流式细胞术分析显示典型的MSC标志物CD73、CD90和CD105的表达。此外,这些细胞几乎没有衰老迹象,培养物通过沿脂肪生成、软骨生成和成骨谱系分化显示出干细胞样特征。
MSC标志物的表达在至少10个冻融/外植体培养周期中得以维持,这表明对预处理的UC组织块进行反复冷冻保存可提供一种可重复且富集的干细胞来源。