Yang Shu-Hua, Chen Po-Quang, Chen Yi-Fang, Lin Feng-Huei
Institute of Biomedical Engineering, College of Engineering and College of Medicine, National Taiwan University, Taipei, Taiwan.
Artif Organs. 2005 Oct;29(10):806-14. doi: 10.1111/j.1525-1594.2005.00133.x.
Tissue engineering approaches for treating degenerative intervertebral discs aim to promote tissue regeneration then retard or even reverse the degenerative process. A gelatin/chondroitin-6-sulfate/hyaluronan tri-copolymer was developed to serve as a bioactive scaffold that could help human nucleus pulposus (NP) cells to preserve their cell viability/proliferation and promote matrix synthesis. Each scaffold was seeded with 1 x 10(6) monolayer-expanded human NP cells and then cultured in vitro. Over a 4-week cultivation period, cell-scaffold hybrids demonstrated active cell viability/proliferation and a progressive increase in net production of glycosaminoglycans. In comparison to monolayer cells, scaffold-cultured cells showed significantly higher mRNA expression in collagen II, aggrecan, Sox9, TGFbeta1, and TIMP1. Expression of mRNA was significantly suppressed in collagen I, collagen X, IL1, and Fas-associating death domain protein. Histological studies showed newly synthesized glycosaminoglycans deposits and collagen II in scaffolds. These results indicate that the tri-copolymer scaffold could be considered as a promising bioactive scaffold for regenerating human NP.
用于治疗退变椎间盘的组织工程方法旨在促进组织再生,进而延缓甚至逆转退变过程。一种明胶/硫酸软骨素-6-硫酸盐/透明质酸三元共聚物被开发用作生物活性支架,其可帮助人髓核(NP)细胞维持细胞活力/增殖并促进基质合成。每个支架接种1×10⁶个单层扩增的人NP细胞,然后进行体外培养。在4周的培养期内,细胞-支架复合物表现出活跃的细胞活力/增殖以及糖胺聚糖净产量的逐步增加。与单层细胞相比,支架培养的细胞在胶原蛋白II、聚集蛋白聚糖、Sox9、转化生长因子β1和金属蛋白酶组织抑制因子1(TIMP1)中显示出显著更高的mRNA表达。在胶原蛋白I、胶原蛋白X、白细胞介素1(IL1)和Fas相关死亡结构域蛋白中,mRNA的表达被显著抑制。组织学研究显示支架中有新合成的糖胺聚糖沉积物和胶原蛋白II。这些结果表明,该三元共聚物支架可被视为用于再生人NP的一种有前景的生物活性支架。