Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Ann Biomed Eng. 2011 Jul;39(7):1872-81. doi: 10.1007/s10439-011-0327-0. Epub 2011 May 18.
Tissue engineering is an effective approach for the treatment of bone defects. Statins have been demonstrated to promote osteoblastic differentiation of bone marrow-derived stromal cells (BMSCs). Electrospun biodegradable fibers have also shown applicability to drug delivery in the form of bone tissue engineered scaffolds with nano- to microscale topography and high porosity similar to the natural extracellular matrix (ECM). The aim of this study was to investigate the feasibility of a simvastatin-releasing, biodegradable, nano- to microscale fiber scaffold (SRBFS) for bone tissue engineering with BMSCs. Simvastatin was released from SRBFS slowly. BMSCs were observed to spread actively and rigidly adhere to SRBFS. BMSCs on SRBFS showed an increase in alkaline phosphatase activity 2 weeks after cell culture. Furthermore, osteoclastogenesis was suppressed by SRBFS in vitro. The new bone formation and mineralization in the SRBFS group were significantly better than in the biodegradable fiber scaffold (BFS) without simvastatin 12 weeks after implantation of the cell-scaffold construct into an ectopic site on the murine back. These results suggest that SRBFS promoted osteoblastic differentiation of BMSCs in vitro and in vivo, and demonstrate feasibility as a bone engineering scaffold.
组织工程是治疗骨缺损的有效方法。他汀类药物已被证明能促进骨髓基质细胞(BMSCs)的成骨细胞分化。电纺生物可降解纤维也显示出适用于以具有纳米到微尺度形貌和类似于天然细胞外基质(ECM)的高孔隙率的骨组织工程支架形式的药物输送。本研究旨在探讨载有辛伐他汀的可生物降解、纳米到微尺度纤维支架(SRBFS)在 BMSCs 骨组织工程中的可行性。辛伐他汀从 SRBFS 中缓慢释放。观察到 BMSCs 积极扩展并牢固地附着在 SRBFS 上。细胞培养 2 周后,BMSCs 的碱性磷酸酶活性增加。此外,SRBFS 在体外抑制破骨细胞生成。植入细胞-支架构建体到鼠背部异位部位 12 周后,SRBFS 组的新骨形成和矿化明显优于没有辛伐他汀的可生物降解纤维支架(BFS)组。这些结果表明,SRBFS 促进了 BMSCs 的体外和体内成骨细胞分化,并证明了作为骨工程支架的可行性。