Song Yang, Wang Xiao-fei, Wang Yu-guang, Sun Yu-chun, Lv Pei-jun
Center of Digital Dentistry,Peking University School and Hospital of Stomatology; National Engineering Laboratory for Digital and Material Technology of Stomatology,Beijing 100081,China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2016 Feb 18;48(1):45-50.
To construct human adipose-derived mesenchymal stem cells (hASCs)-biomaterial mixture 3D bio-printing body and detect its osteogenesis in vivo, and to establish a guideline of osteogenesis in vivo by use of 3D bio-printing technology preliminarily.
P4 hASCs were used as seed cells, whose osteogenic potential in vitro was tested by alkaline phosphatase (ALP) staining and alizarin red staining after 14 d of osteogenic induction. The cells were added into 20 g/L sodium alginate and 80 g/L gelatin mixture (cell density was 1 × 10(6)/mL), and the cell-sodium alginate-gelatin mixture was printed by Bioplotter 3D bio-printer (Envision company, Germany), in which the cells'survival rate was detected by live- dead cell double fluorescence staining. Next, the printing body was osteogenically induced for 1 week to gain the experimental group; and the sodium alginate-gelatin mixture without cells was also printed to gain the control group. Both the experimental group and the control group were implanted into the back of the nude mice. After 6 weeks of implantation, the samples were collected, HE staining, Masson staining, immunohistochemical staining and Inveon Micro CT test were preformed to analyze their osteogenic capability.
The cells'survival rate was 89%± 2% after printing. Six weeks after implantation, the samples of the control group were mostly degraded, whose shape was irregular and gel-like; the samples of the experimental group kept their original size and their texture was tough. HE staining and Masson staining showed that the bone-like tissue and vessel in-growth could be observed in the experimental group 6 weeks after implantation, immunohistochemical staining showed that the result of osteocalcin was positive, and Micro CT results showed that samples of the experimental group had a higher density and the new bone volume was 18% ± 1%.
hASCs -biomaterial mixture 3D bio-printing body has capability of ectopic bone formation in nude mice, and it is feasible to apply cells-biomaterial mixture 3D bio-printing technology in the area of bone formation in vivo.
构建人脂肪间充质干细胞(hASCs)-生物材料混合物三维生物打印体并检测其体内成骨情况,初步建立利用三维生物打印技术进行体内成骨的指导原则。
采用第4代hASCs作为种子细胞,成骨诱导14 d后通过碱性磷酸酶(ALP)染色和茜素红染色检测其体外成骨潜能。将细胞加入20 g/L海藻酸钠和80 g/L明胶混合物(细胞密度为1×10⁶/mL)中,通过德国Envision公司的Bioplotter三维生物打印机打印细胞-海藻酸钠-明胶混合物,采用活死细胞双荧光染色检测细胞存活率。接着,将打印体进行1周的成骨诱导以获得实验组;同时打印不含细胞的海藻酸钠-明胶混合物以获得对照组。将实验组和对照组均植入裸鼠背部。植入6周后,收集样本,进行苏木精-伊红(HE)染色、Masson染色、免疫组织化学染色及Inveon Micro CT检测,分析其成骨能力。
打印后细胞存活率为89%±2%。植入6周后,对照组样本大多降解,形状不规则且呈凝胶状;实验组样本保持原有大小,质地坚韧。HE染色和Masson染色显示,植入6周后实验组可见类骨组织及血管长入,免疫组织化学染色显示骨钙素结果为阳性,Micro CT结果显示实验组样本密度更高,新骨体积为18%±1%。
hASCs-生物材料混合物三维生物打印体在裸鼠体内具有异位成骨能力,将细胞-生物材料混合物三维生物打印技术应用于体内骨形成领域是可行的。