Trinity Centre for Bioengineering, School of Engineering, Trinity College Dublin, Dublin 2, Ireland.
Biotechnol Appl Biochem. 2011 Sep-Oct;58(5):345-52. doi: 10.1002/bab.45. Epub 2011 Sep 23.
Articular cartilage has a limited capacity for self-renewal and repair. Tissue engineering of cartilage in vitro has been proposed as a solution to this problem; however, this approach is costly and requires a significant amount of time to grow the graft. An alternative approach is to implant chondroprogenitor cells seeded within a growth factor delivery scaffold directly into the defect site to promote tissue regeneration. The objective of this study was to develop a biocompatible growth factor delivery system capable of promoting chondrogenesis of infrapatellar fat pad (IFP)-derived stem cells. Transforming growth factor beta-1 (TGF-β1) was loaded into gelatin microspheres and incorporated into fibrin hydrogels containing IFP-derived stem cells. The release of TGF-β1 was quantified using an enzyme-linked immunosorbent assay, whereas chondrogenesis was demonstrated histologically and by quantifying sulfated glycosaminoglycan production after 21 days of in vitro culture. TGF-β1 loaded into gelatin microspheres appeared to be as effective in promoting chondrogenesis of IFP-derived stem cells as adding TGF-β1 directly to the medium. The influence of different microsphere fabrication parameters and TGF-β1 loading concentrations was also investigated but appeared to only have a small effect on subsequent chondrogenesis. The development of such growth factor delivery systems in combination with IFP-derived stem cells represents a potential new strategy for cartilage defect repair.
关节软骨自我更新和修复的能力有限。体外软骨组织工程被提出作为解决这个问题的一种方法;然而,这种方法成本高,需要大量的时间来生长移植物。另一种方法是将种植在生长因子递送支架内的软骨祖细胞直接植入缺陷部位,以促进组织再生。本研究的目的是开发一种能够促进髌下脂肪垫(IFP)来源的干细胞软骨形成的生物相容性生长因子递送系统。转化生长因子β-1(TGF-β1)被加载到明胶微球中,并与含有 IFP 来源的干细胞的纤维蛋白水凝胶结合。使用酶联免疫吸附试验定量测定 TGF-β1 的释放,而在体外培养 21 天后通过组织学和硫酸化糖胺聚糖产生的定量来证明软骨形成。负载到明胶微球中的 TGF-β1 似乎与直接将 TGF-β1 添加到培养基中一样有效地促进 IFP 来源的干细胞的软骨形成。还研究了不同的微球制造参数和 TGF-β1 加载浓度的影响,但似乎对随后的软骨形成只有很小的影响。这种生长因子递送系统与 IFP 来源的干细胞相结合的开发代表了软骨缺损修复的一种新的潜在策略。