Miyazawa Atsuko, Matsuno Tomonori, Asano Kazunari, Tabata Yasuhiko, Satoh Tazuko
Department of Oral & Maxillofacial Surgery, The Nippon Dental University School of Life Dentistry.
Dent Mater J. 2015;34(4):466-74. doi: 10.4012/dmj.2014-272.
The objective of this study was to investigate the odontoblastic differentiation of dental pulp stem cells (DPSC) by biodegradable hydrogels incorporating simvastatin micelles, both in vitro and in vivo. Simvastatin (ST) was incorporated into the micelles of gelatin grafted with L-lactic acid oligomers (LAo) to allow water-solubilization. The simvastatin-LAo-grafted gelatin (LAo-g-gelatin) micelles were mixed with gelatin, followed by chemical crosslinking to form gelatin hydrogels (ST Mi/GH). The ST Mi were released from the gelatin hydrogel granules (GH) through enzymatic degradation. The ST Mi enhanced alkaline phosphatase activity, calcium deposition, and bone morphogenic protein-2 secretion of DPSC. When implanted subcutaneously into mice, the ST Mi/GH treated group exhibited increased dentin sialoprotein and calcium deposition, compared with those treated with GH plus free ST. It is possible to achieve odontoblastic differentiation of DPSC through the controlled release of ST from GH.
本研究的目的是在体外和体内研究通过掺入辛伐他汀胶束的可生物降解水凝胶诱导牙髓干细胞(DPSC)向成牙本质细胞分化。将辛伐他汀(ST)掺入接枝有L-乳酸低聚物(LAo)的明胶胶束中以实现水溶性。将辛伐他汀-LAo接枝明胶(LAo-g-明胶)胶束与明胶混合,然后进行化学交联以形成明胶水凝胶(ST Mi/GH)。ST Mi通过酶促降解从明胶水凝胶颗粒(GH)中释放出来。ST Mi增强了DPSC的碱性磷酸酶活性、钙沉积和骨形态发生蛋白-2分泌。当皮下植入小鼠时,与用GH加游离ST处理的组相比,ST Mi/GH处理组的牙本质涎蛋白和钙沉积增加。通过从GH中控制释放ST可以实现DPSC的成牙本质细胞分化。