Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
J Control Release. 2012 Mar 10;158(2):224-32. doi: 10.1016/j.jconrel.2011.11.003. Epub 2011 Nov 10.
Self-assembling cell sheets have shown great potential for use in cartilage tissue engineering applications, as they provide an advantageous environment for the chondrogenic induction of human mesenchymal stem cells (hMSCs). We have engineered a system of self-assembled, microsphere-incorporated hMSC sheets capable of forming cartilage in the presence of exogenous transforming growth factor β1 (TGF-β1) or with TGF-β1 released from incorporated microspheres. Gelatin microspheres with two different degrees of crosslinking were used to enable different cell-mediated microsphere degradation rates. Biochemical assays, histological and immunohistochemical analyses, and biomechanical testing were performed to determine biochemical composition, structure, and equilibrium modulus in unconfined compression after 3 weeks of culture. The inclusion of microspheres with or without loaded TGF-β1 significantly increased sheet thickness and compressive equilibrium modulus, and enabled more uniform matrix deposition by comparison to control sheets without microspheres. Sheets incorporated with fast-degrading microspheres containing TGF-β1 produced significantly more GAG and GAG per DNA than all other groups tested and stained more intensely for type II collagen. These findings demonstrate improved cartilage formation in microsphere-incorporated cell sheets, and describe a tailorable system for the chondrogenic induction of hMSCs without necessitating culture in growth factor-containing medium.
自组装细胞片层在软骨组织工程应用中显示出巨大的潜力,因为它们为人类间充质干细胞(hMSC)的软骨诱导提供了有利的环境。我们构建了一种自组装的、包含微球的 hMSC 片层系统,该系统能够在存在外源性转化生长因子 β1(TGF-β1)或包含微球释放的 TGF-β1 的情况下形成软骨。使用两种不同交联程度的明胶微球来实现不同的细胞介导的微球降解速率。进行了生化分析、组织学和免疫组织化学分析以及无约束压缩下的生物力学测试,以确定培养 3 周后的生化组成、结构和平衡模量。与不含微球的对照片层相比,包含负载 TGF-β1 的微球或不包含 TGF-β1 的微球的片层显著增加了片层厚度和压缩平衡模量,并能够更均匀地沉积基质。含有 TGF-β1 的快速降解微球的片层产生的 GAG 和 GAG 每 DNA 显著高于所有其他测试组,并且对 II 型胶原的染色更强烈。这些发现表明,微球掺入细胞片层中可改善软骨形成,并描述了一种可定制的 hMSC 软骨诱导系统,而无需在含生长因子的培养基中培养。