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作 者:刘曦明[1] 罗飞[1] 曾玲[1] 谢肇[1] 陈庄洪 许建中[1] 李起鸿[1]
机构地区:[1]第三军医大学西南医院骨科全军矫形外科中心 [2]解放军武汉总医院骨科
出 处:《中国中医骨伤科杂志》2008年第3期31-34,共4页Chinese Journal of Traditional Medical Traumatology & Orthopedics
基 金:国家高技术研究发展计划(863计划)重大攻关课题(2006AA02A122)
摘 要:目的:评价多聚赖氨酸修饰的脱钙骨基质富集材料的细胞毒性,为该材料应用于临床提供实验依据。方法:参照GB/T16886.5-2003-ISO 10993-5:1999标准,将不同浓度的材料浸提液分别与人间充质干细胞(MSCs),成骨细胞(OS)体外复合培养。倒置相差显微镜行细胞形态学观察;MTT比色法测定1、3、5、7d的MSCs增殖活性;金氏比色法检测OS碱性磷酸酶活性。结果:不同时间点、不同浓度材料浸提液培养的MSCs均良好增殖,毒性0~1级;5d后浸提液培养组细胞增殖率优于阴性对照组(P<0.05),随材料浸提液浓度增加而增加;浸提液培养组OS碱性磷酸酶活性与阴性对照组相比差异无显著性(P>0.05)。结论:经多聚赖氨酸修饰的脱钙骨基质富集支架材料无细胞毒性,实验浓度范围内利于MSCs增殖,不影响OS的成骨活性。Objective: To evaluate the cytotoxicity of decalcified bone matrix decorated with poly-L-lysine in order to provide experimental proof for its clinical application. Methods: According to the criteria for evaluation of cellular trials recommended in GB/T16886.5--2003--ISO 10993--5:1999, the mesenchymal stem cells (MSCs) and osteoblast cells (OS) were cocultured with different doses of extracts of decalcified bone matrix decorated with poly-L-lysine in vitro. Cell morphology were observed by invert phase contrast microscope, MSCs proliferation and relative multiplication rate were calculated with MTT assay at 1, 3, 5 and 7 days. The activity of alkaline phosphatase (ALP) in OS was tested at the same time. Results: The growth and proliferation of MSCs were normal in different doses of extracts at different time point, levels of toxicity ranged from 0 to 1 grade. Relative multiplication rate of MSCs co-cultured with extracts was significantly higher than that without extracts after 5 days (P^0.05) and went higher as the extract dose denser. There was no obvious difference in ALP activity between OS co-cultured with and without extracts. Conclusion: The decalcified bone matrix decorated with poly-L-lysine showed no cytotoxicity and within experimental density, it could promote the proliferation of MSCs without affecting osteogenesis activity of OS.
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