Sridharan BanuPriya, Laflin Amy D, Detamore Michael S
Bioengineering Program, University of Kansas, Lawrence, KS 66045 USA.
Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, KS 66045 USA.
Cell Mol Bioeng. 2018 Apr;11(2):99-115. doi: 10.1007/s12195-017-0517-4. Epub 2017 Dec 22.
Spheroids of mesenchymal stem cells (MSCs) in cartilage tissue engineering have been shown to enhance regenerative potential owing to their 3D structure. In this study, we explored the possibility of priming spheroids under different media to replace the use of inductive surface coatings for chondrogenic differentiation.
Rat bone marrow-derived MSCs were organized into cell spheroids by the hanging drop technique and subsequently cultured on hyaluronic acid (HA) coated or non-coated well plates under different cell media conditions. Endpoint analysis included cell viability, DNA and Glycosaminoglycan (GAG) and collagen content, gene expression and immunohistochemistry.
For chondrogenic applications, MSC spheroids derived on non-coated surfaces outperformed the spheroids derived from HA-coated surfaces in matrix synthesis and collagen II gene expression. Spheroids on non-coated surfaces gave rise to the highest collagen and GAG when primed with medium containing insulin-like growth factor (IGF) for 1 week during spheroid formation. Spheroids that were grown in chondroinductive raw material-inclusive media such as aggrecan or chondroitin sulfate exhibited the highest Collagen II gene expression in the non-coated surface at 1 week.
Media priming by growth factors and raw materials might be a more predictive influencer of chondrogenesis compared to inductive-surfaces. Such tailored bioactivity of the stem cell spheroids in the stage of the spheroid formation may give rise to a platform technology that may eventually produce spheroids capable of chondrogenesis achieved by mere media manipulation, skipping the need for additional culture on a modified surface, that paves the way for cost-effective technologies.
软骨组织工程中,间充质干细胞(MSCs)球体因其三维结构已显示出增强的再生潜力。在本研究中,我们探索了在不同培养基中预处理球体以替代使用诱导性表面涂层进行软骨分化的可能性。
通过悬滴技术将大鼠骨髓来源的间充质干细胞组织成细胞球体,随后在不同细胞培养基条件下,在透明质酸(HA)包被或未包被的孔板上培养。终点分析包括细胞活力、DNA、糖胺聚糖(GAG)和胶原蛋白含量、基因表达及免疫组织化学。
对于软骨生成应用,在非包被表面衍生的间充质干细胞球体在基质合成和胶原蛋白II基因表达方面优于在HA包被表面衍生的球体。在球体形成过程中,用含胰岛素样生长因子(IGF)的培养基预处理1周时,非包被表面的球体产生的胶原蛋白和GAG最高。在含聚集蛋白聚糖或硫酸软骨素等软骨诱导原料的培养基中生长的球体,在第1周时在非包被表面表现出最高的胶原蛋白II基因表达。
与诱导性表面相比,生长因子和原料对培养基的预处理可能是软骨生成更具预测性的影响因素。干细胞球体在球体形成阶段的这种定制生物活性可能会产生一种平台技术,最终可能通过单纯的培养基操作产生能够软骨生成的球体,无需在修饰表面上进行额外培养,这为具有成本效益的技术铺平了道路。