Pan Haitao, Zheng Qixin, Yang Shuhua, Guo Xiaodong
Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
J Biomed Mater Res A. 2014 Dec;102(12):4526-35. doi: 10.1002/jbm.a.35129. Epub 2014 Feb 28.
Functionalization of polymer surfaces has been recognized as a valuable tool to improve their properties that significantly influence cellular behaviors, such as adhesion, proliferation, migration, and differentiation. In stem cell-mediated bone tissue engineering, surface multifunctionalization of polymeric scaffolds with cell-adhesive, osteoconductive, and osteoinductive biomolecules is a critical strategy to improve such properties. However, the traditional surface modification techniques such as physical deposition/adsorption, chemical modification, grafting, and plasma techniques have great limitations for immobilization of multiple bioactive molecules due to multistep procedures. Recently, a universal technique based on mussel-inspired self-polymerization of dopamine is developed for multifunctional coatings in a simple way. In our study, we used this newly developed technique to incorporate three biomolecules, cell adhesion-promoting (K)16 GRGDSPC peptides, osteoconductive hydroxyapatite (HAp) nanoparticles, and osteoinductive bone morphogenetic protein-2-derived P24 peptides, to functionalize poly(lactide-co-glycolide) (PLGA)-[Asp-PEG]n scaffolds, and the effects on biological behaviors of co-cultured rabbit-derived bone marrow stromal cells in vitro were investigated. The results showed (K)16 GRGDSPC, HAp, and P24 could be immobilized onto the scaffolds through predeposition of polydopamine (pDA) ad-layer, and the surface-modified scaffolds were noncytotoxic as well as the virgin scaffold. The pDA-assisted codeposition of (K)16 GRGDSPC, HAp, and P24 on the scaffold surfaces significantly promoted cell adhesion, proliferation, osteodifferentiation, and mineralization in vitro with synergistic effects. Taken together, the functionalized PLGA-[Asp-PEG]n polymeric scaffolds achieved significantly elevated affinity, osteoconductive and osteoinductive ability, and may be a potentially promising bone graft substitute for bone repair.
聚合物表面功能化已被视为一种有价值的工具,可用于改善其显著影响细胞行为(如粘附、增殖、迁移和分化)的性能。在干细胞介导的骨组织工程中,用具有细胞粘附性、骨传导性和骨诱导性的生物分子对聚合物支架进行表面多功能化是改善这些性能的关键策略。然而,传统的表面改性技术,如物理沉积/吸附、化学改性、接枝和等离子体技术,由于步骤繁多,在固定多种生物活性分子方面存在很大局限性。最近,一种基于贻贝启发的多巴胺自聚合的通用技术被开发出来,用于以简单的方式制备多功能涂层。在我们的研究中,我们使用这种新开发的技术将三种生物分子,即促进细胞粘附的(K)16 GRGDSPC肽、骨传导性羟基磷灰石(HAp)纳米颗粒和骨诱导性骨形态发生蛋白-2衍生的P24肽,整合到聚(丙交酯-共-乙交酯)(PLGA)-[Asp-PEG]n支架上,并研究了其对体外共培养的兔源骨髓基质细胞生物学行为的影响。结果表明,(K)16 GRGDSPC、HAp和P24可以通过聚多巴胺(pDA)吸附层的预沉积固定在支架上,并且表面改性的支架与原始支架一样无细胞毒性。pDA辅助(K)16 GRGDSPC、HAp和P24在支架表面的共沉积显著促进了体外细胞粘附、增殖、骨分化和矿化,并具有协同作用。综上所述,功能化的PLGA-[Asp-PEG]n聚合物支架实现了显著提高的亲和力、骨传导和骨诱导能力,可能是一种潜在的有前途的骨移植替代物用于骨修复。