Jang Ja Yong, Park Seung Hun, Park Ji Hoon, Lee Bo Keun, Yun Jeong-Ho, Lee Bong, Kim Jae Ho, Min Byoung Hyun, Kim Moon Suk
Department of Molecular Science and Technology, Ajou University, Suwon, 443-759, Korea.
Department of Periodontology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University, Jeonju, 561-712, Korea.
Macromol Biosci. 2016 Aug;16(8):1158-69. doi: 10.1002/mabi.201600001. Epub 2016 Apr 14.
In this study, human dental pulp stem cells (hDPSCs) are examined as a cellular source for bone tissue engineering using an in vivo-forming hydrogel. The hDPSCs are easily harvested in large quantities from extracted teeth. The stemness of harvested hDPSCs indicates their relative tolerance to ex vivo manipulation in culture. The in vitro osteogenic differentiation of hDPSCs is characterized using Alizarin Red S (ARS), von Kossa (VK), and alkaline phosphatase (ALP) staining. The solution of hDPSCs and a methoxy polyethylene glycol-polycaprolactone block copolymer (PC) is easily prepared by simple mixing at room temperature and in no more than 10 s it forms in vivo hydrogels after subcutaneous injection into rats. In vivo osteogenic differentiation of hDPSCs in the in vivo-forming hydrogel is confirmed by micro-computed tomography (CT), histological staining, and gene expression. Micro-CT analysis shows evidence of significant tissue-engineered bone formation in hDPSCs-loaded hydrogel in the presence of osteogenic factors. Differentiated osteoblasts in in vivo-forming hydrogel are identified by ARS and VK staining and are found to exhibit characteristic expression of genes like osteonectin, osteopontin, and osteocalcin. In conclusion, hDPSCs embedded in an in vivo-forming hydrogel may provide benefits as a noninvasive formulation for bone tissue engineering applications.
在本研究中,使用一种可在体内形成的水凝胶,将人牙髓干细胞(hDPSCs)作为骨组织工程的细胞来源进行了研究。hDPSCs很容易从拔除的牙齿中大量获取。所获取的hDPSCs的干性表明它们在体外培养操作中具有相对耐受性。使用茜素红S(ARS)、冯科萨(VK)和碱性磷酸酶(ALP)染色对hDPSCs的体外成骨分化进行了表征。hDPSCs溶液与甲氧基聚乙二醇-聚己内酯嵌段共聚物(PC)通过在室温下简单混合即可轻松制备,皮下注射到大鼠体内后,在不超过10秒内就会形成体内水凝胶。通过微型计算机断层扫描(CT)、组织学染色和基因表达证实了hDPSCs在体内形成的水凝胶中的体内成骨分化。微型CT分析显示,在存在成骨因子的情况下,负载hDPSCs的水凝胶中有显著的组织工程化骨形成的证据。通过ARS和VK染色鉴定了体内形成的水凝胶中分化的成骨细胞,并发现它们表现出骨连接蛋白、骨桥蛋白和骨钙素等基因的特征性表达。总之,嵌入体内形成的水凝胶中的hDPSCs作为骨组织工程应用的非侵入性制剂可能具有优势。