RP技术制备PDLLA/TCP人工骨载体与LDPTH成骨效应相容性的体外实验
骨髓基质细胞,,载体;PTH;骨髓基质细胞;间隙连接蛋白,0引言,1材料和方法,2结果,3讨论,【参考文献】
Biocompatibility of RP manufactured PDLLA/TCP tissue engineered bone scaffolds in low dose PTHinduced bone anabolism in vitroMA Xing, HU YunYu, YAN YongNian, XIONG Zhuo, Lü Rong, WANG Jun, XU XinZhi, BAI JianPing
1PLA Institute of Orthopaedics, Xijing Hospital, Fourth Military Medical University, Xian 710033, China, 2Laser Rapid Prototyping Biomanufacturing Center, School of Mechanical Engineering, Tsinghua University, Beijing 100084, China
【Abstract】 AIM: To investigate the cell biocompatibility of tissue engineered bone scaffolds in lowdose parathyroid hormone (LDPTH)induced bone formation activities in vitro. METHODS: Tridimensional PDLLA/TCP scaffolds (with component ratio of 7∶3) were synthesized by RP and observed by scanning electron microscopy. Human bone marrow stromal cells (MSCs) were primarily cultured and divided into four groups according to the different mode of exposure. The four groups were: Group A, control culture group; Group B: PDLLA/TCP immersed medium culture group; Group C: LDPTH [10 nmol/L hPTH (1-34)] intermittent exposure group; and Group D: LDPTH+PDLLA/TCP immersed medium culture group. A 48 h incubation cycle was repeated 8 times in 4 groups and the cell proliferation, gap junctional intercellular communication (GJIC) and bone like formation activities in vitro were detected by number of cell doubling (NCD), Lucifer Yellow (LY) scrape loading dye transfer (SLDT) and Von Kossa staining, respectively. RESULTS: The PDLLA/TCP scaffolds established by RP technology had good biomaterial properties such as satisfactory microstructure and porosities. The PDLLA/TCP immersed culture medium had no significant negative effects on cell growth (P>0.05) and functional differentiation in the presence of LDPTH. CONCLUSION: PDLLA/TCP composite scaffolds established by RP have ideal microstructure, porosities and cell biocompatibilities in LDPTH stimulated bone formation activities. ......
您现在查看是摘要页,全文长 11812 字符。