France L A, Scotchford C A, Grant D M, Rashidi H, Popov A A, Sottile V
Division of Materials, Mechanics and Structures, Faculty of Engineering, University of Nottingham, UK.
J Tissue Eng Regen Med. 2014 Aug;8(8):652-63. doi: 10.1002/term.1567. Epub 2012 Nov 14.
Human mesenchymal stem cells (MSCs), which can generate both osteoblasts and chondrocytes, represent an ideal resource for orthopaedic repair using tissue-engineering approaches. One major difficulty for the development of osteochondral constructs using undifferentiated MSCs is that serum is typically used in culture protocols to promote differentiation of the osteogenic component, whereas existing chondrogenic differentiation protocols rely on the use of serum-free conditions. In order to define conditions which could be compatible with both chondrogenic and osteogenic differentiation in a single bioreactor, we have analysed the efficiency of new biphasic differentiation regimes based on transient serum exposure followed by serum-free treatment. MSC differentiation was assessed either in serum-free medium or with a range of transient exposure to serum, and compared to continuous serum-containing treatment. Although osteogenic differentation was not supported in the complete absence of serum, marker expression and extensive mineralization analyses established that 5 days of transient exposure triggered a level of differentiation comparable to that observed when serum was present throughout. This initial phase of serum exposure was further shown to support the successful chondrogenic differentiation of MSCs, comparable to controls maintained in serum-free conditions throughout. This study indicates that a culture based on temporal serum exposure followed by serum-free treatment is compatible with both osteogenic and chondrogenic differentiation of MSCs. These results will allow the development of novel strategies for osteochondral tissue engineering approaches using MSCs for regenerative medicine.
人间充质干细胞(MSCs)能够生成成骨细胞和软骨细胞,是采用组织工程方法进行骨科修复的理想细胞来源。利用未分化的间充质干细胞构建骨软骨组织面临的一个主要困难在于,培养方案中通常使用血清来促进成骨成分的分化,而现有的软骨分化方案则依赖于无血清条件。为了确定在单个生物反应器中能够同时兼容软骨生成和成骨分化的条件,我们分析了基于短暂血清暴露随后进行无血清处理的新型双相分化方案的效率。在无血清培养基中或短暂暴露于一系列血清浓度下评估间充质干细胞的分化情况,并与持续含血清处理进行比较。尽管在完全无血清的情况下无法支持成骨分化,但标志物表达和广泛的矿化分析表明,5天的短暂血清暴露引发的分化水平与全程存在血清时观察到的相当。血清暴露的初始阶段进一步表明能够支持间充质干细胞成功进行软骨生成分化,与全程维持在无血清条件下的对照组相当。这项研究表明,基于短暂血清暴露随后进行无血清处理的培养方式与间充质干细胞的成骨和软骨生成分化均兼容。这些结果将有助于开发利用间充质干细胞进行再生医学的骨软骨组织工程新策略。