Almeida Henrique V, Liu Yurong, Cunniffe Gráinne M, Mulhall Kevin J, Matsiko Amos, Buckley Conor T, O'Brien Fergal J, Kelly Daniel J
Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland; Department of Mechanical and Manufacturing Engineering, School of Engineering, Trinity College Dublin, Dublin 2, Ireland.
Sports Surgery Clinic, Santry, Dublin 9, Ireland.
Acta Biomater. 2014 Oct;10(10):4400-9. doi: 10.1016/j.actbio.2014.05.030. Epub 2014 Jun 4.
The objective of this study was to develop a scaffold derived from cartilaginous extracellular matrix (ECM) that could be used as a growth factor delivery system to promote chondrogenesis of stem cells. Dehydrothermal crosslinked scaffolds were fabricated using a slurry of homogenized porcine articular cartilage, which was then seeded with human infrapatellar-fat-pad-derived stem cells (FPSCs). It was found that these ECM-derived scaffolds promoted superior chondrogenesis of FPSCs when the constructs were additionally stimulated with transforming growth factor (TGF)-β3. Cell-mediated contraction of the scaffold was observed, which could be limited by the additional use of 1-ethyl-3-3dimethyl aminopropyl carbodiimide (EDAC) crosslinking without suppressing cartilage-specific matrix accumulation within the construct. To further validate the utility of the ECM-derived scaffold, we next compared its chondro-permissive properties to a biomimetic collagen-hyaluronic acid (HA) scaffold optimized for cartilage tissue engineering (TE) applications. The cartilage-ECM-derived scaffold supported at least comparable chondrogenesis to the collagen-HA scaffold, underwent less contraction and retained a greater proportion of synthesized sulfated glycosaminoglycans. Having developed a promising scaffold for TE, with superior chondrogenesis observed in the presence of exogenously supplied TGF-β3, the final phase of the study explored whether this scaffold could be used as a TGF-β3 delivery system to promote chondrogenesis of FPSCs. It was found that the majority of TGF-β3 that was loaded onto the scaffold was released in a controlled manner over the first 10days of culture, with comparable long-term chondrogenesis observed in these TGF-β3-loaded constructs compared to scaffolds where the TGF-β3 was continuously added to the media. The results of this study support the use of cartilage-ECM-derived scaffolds as a growth factor delivery system for use in articular cartilage regeneration.
本研究的目的是开发一种源自软骨细胞外基质(ECM)的支架,该支架可作为生长因子递送系统,以促进干细胞的软骨生成。使用匀浆的猪关节软骨制成脱水热交联支架,然后接种人髌下脂肪垫来源的干细胞(FPSC)。结果发现,当构建体用转化生长因子(TGF)-β3额外刺激时,这些源自ECM的支架能促进FPSC的软骨生成。观察到支架的细胞介导收缩,可通过额外使用1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDAC)交联来限制,而不抑制构建体内软骨特异性基质的积累。为了进一步验证源自ECM的支架的效用,接下来我们将其软骨允许特性与针对软骨组织工程(TE)应用优化的仿生胶原-透明质酸(HA)支架进行了比较。源自软骨ECM的支架支持至少与胶原-HA支架相当的软骨生成,收缩较少,并保留了更大比例的合成硫酸化糖胺聚糖。在开发出一种有前景的用于TE的支架后,在外源供应TGF-β3的情况下观察到了卓越的软骨生成,研究的最后阶段探讨了这种支架是否可用作TGF-β3递送系统来促进FPSC的软骨生成。结果发现,加载到支架上的大部分TGF-β3在培养的前10天以可控方式释放,与将TGF-β3持续添加到培养基中的支架相比,在这些加载TGF-β3的构建体中观察到了相当的长期软骨生成。本研究结果支持将源自软骨ECM的支架用作关节软骨再生的生长因子递送系统。